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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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of the spine in children are rare, and further clinical description is necessary. This study investigated epidemiology, interventions, and outcomes of pediatric patients with spine and spinal cord tumors. The National Inpatient Sample and Kids’ Inpatient Database were used for the study. Outcomes were studied, and bivariate significant trends were analyzed in a multivariate setting. Analysis of 2870 patients between 2000 and 2009 found a median age of diagnosis of 11 years (Tables 1 and 2). Most were white (65.2%) and had private insurance (62.3%), and 46.8% of procedures were emergent operations. Treatment occurred at teaching (93.6%) and non-children’s hospitals (81.1%). Overall mortality rate was 1.7%, non-routine discharges occurred at a rate 19.9%, complications at 21.1%, and average total charges were $66,087. A majority of patients (87.5%) had no intervention, and of those patients receiving treatment, 78.2% underwent surgery and 23.1% had radiotherapy. Treatment with surgery alone increased significantly over time (p \u003C 0.0001). Odds ratio (OR) of mortality was significantly higher in 2006 (OR 3.5) and 2009 (OR 2.6) when compared to 2000. Complications (OR 7.9) and disease comorbidities (OR 1.5) were associated with significantly increased odds of mortality. Hospital characteristics, length of stay, and charges remained relatively unchanged. In recent years, there has been a decreasing incidence of spine and spinal cord tumors in children. Notably, a higher mortality rate is evident over time in addition to an increase in the proportion of patients undergoing surgery. The high percentage of emergent operations suggests a weak recognition of spine tumors in children and should prompt a call for increased awareness of this cancer. In spite of these findings, lack of tumor type identification was a limitation to this study.",{"EN":1214},"Treatment patterns of children with spine and spinal cord tumors: national outcomes and review of the literature",{"VOID":1216},"Hayden Gephart MG, Lober RM, Arrigo RT et al (2012) Trends in the diagnosis and treatment of pediatric primary spinal cord tumors. J Neurosurg Pediatr 10:555–559. doi:10.3171\u002F2012.9.PEDS1272\nHsu S, Quattrone M, Ostrom Q et al (2011) Incidence patterns for primary malignant spinal cord gliomas: a Surveillance, Epidemiology, and End Results study. J Neurosurg Spine 14:742–747. doi:10.3171\u002F2011.1.SPINE10351\nDolecek TA, Propp JM, Stroup NE, Kruchko C (2012) CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005-2009. Neuro-Oncology 14(Suppl 5):v1–49. doi:10.1093\u002Fneuonc\u002Fnos218\nSchellinger KA, Propp JM, Villano JL, McCarthy BJ (2008) Descriptive epidemiology of primary spinal cord tumors. J Neuro-Oncol 87:173–179. doi:10.1007\u002Fs11060-007-9507-z\nSpacca B, Giordano F, Donati P, Genitori L (2015) Spinal tumors in children: long-term retrospective evaluation of a series of 134 cases treated in a single unit of pediatric neurosurgery. Spine J 15:1949–1955. doi:10.1016\u002Fj.spinee.2015.04.012\nAhmed R, Menezes AH, Awe OO et al (2014) Long-term incidence and risk factors for development of spinal deformity following resection of pediatric intramedullary spinal cord tumors. J Neurosurg Pediatr 13:613–621. doi:10.3171\u002F2014.1.PEDS13317\nAhmed R, Menezes AH, Awe OO, Torner JC (2014) Long-term disease and neurological outcomes in patients with pediatric intramedullary spinal cord tumors. J Neurosurg Pediatr 13:600–612. doi:10.3171\u002F2014.1.PEDS13316\nSchneider C, Hidalgo ET, Schmitt-Mechelke T, Kothbauer KF (2014) Quality of life after surgical treatment of primary intramedullary spinal cord tumors in children. J Neurosurg Pediatr 13:170–177. doi:10.3171\u002F2013.11.PEDS13346\nStephen JH, Sievert AJ, Madsen PJ et al (2012) Spinal cord ependymomas and myxopapillary ependymomas in the first 2 decades of life: a clinicopathological and immunohistochemical characterization of 19 cases. J Neurosurg Pediatr 9:646–653. doi:10.3171\u002F2012.2.PEDS11285\nChoi GH, Oh JK, Kim TY et al (2012) The clinical features and surgical outcomes of pediatric patients with primary spinal cord tumor. Childs Nerv Syst 28:897–904. doi:10.1007\u002Fs00381-012-1718-8\nCasha S, Phan N, Rutka J (2006) Spinal cord and column tumors in children. Thieme 1:187–203\nÖzkan N, Jabbarli R, Wrede KH et al (2015) Surgical management of intradural spinal cord tumors in children and young adults: a single-center experience with 50 patients. Surg Neurol Int 6:F–7. doi:10.4103\u002F2152-7806.171236\nSahu RK, Das KK, Bhaisora KS et al Pediatric intramedullary spinal cord lesions: pathological spectrum and outcome of surgery. J Pediatr Neurosci 10:214–221. doi:10.4103\u002F1817-1745.165660\nKutluk T, Varan A, Kafali C et al (2015) Pediatric intramedullary spinal cord tumors: a single center experience. Eur J Paediatr Neurol 19:41–47. doi:10.1016\u002Fj.ejpn.2014.09.007\nShin JI, Lee NJ, Cho SK (2016) Pediatric cervical spine and spinal cord injury: a national database study. Spine (Phila Pa 1976) 41:283–292. doi:10.1097\u002FBRS.0000000000001176\nLarson AN, Polly DW, Ackerman SJ et al (2016) What would be the annual cost savings if fewer screws were used in adolescent idiopathic scoliosis treatment in the US? J Neurosurg Spine 24:116–123. doi:10.3171\u002F2015.4.SPINE131119\nPiatt JH (2015) Pediatric spinal injury in the US: epidemiology and disparities. J Neurosurg Pediatr 16:463–471. doi:10.3171\u002F2015.2.PEDS1515\nFord JB, Roberts CL, Algert CS et al (2007) Using hospital discharge data for determining neonatal morbidity and mortality: a validation study. BMC Health Serv Res 7:188. doi:10.1186\u002F1472-6963-7-188\nLundar T, Due-Tønnessen BJ, Scheie D, Brandal P (2014) Pediatric spinal ependymomas: an unpredictable and puzzling disease. Long-term follow-up of a single consecutive institutional series of ten patients. Childs Nerv Syst 30:2083–2088. doi:10.1007\u002Fs00381-014-2491-7\nSurawicz TS, McCarthy BJ, Kupelian V et al (1999) Descriptive epidemiology of primary brain and CNS tumors: results from the Central Brain Tumor Registry of the United States, 1990-1994. Neuro-Oncology 1:14–25\nGarcés-Ambrossi GL, McGirt MJ, Mehta VA et al (2009) Factors associated with progression-free survival and long-term neurological outcome after resection of intramedullary spinal cord tumors: analysis of 101 consecutive cases. J Neurosurg Spine 11:591–599. doi:10.3171\u002F2009.4.SPINE08159\nMilano MT, Johnson MD, Sul J et al (2010) Primary spinal cord glioma: a surveillance, epidemiology, and end results database study. J Neuro-Oncol 98:83–92. doi:10.1007\u002Fs11060-009-0054-7\nLin Y, Jea A, Melkonian SC, Lam S (2015) Treatment of pediatric grade II spinal ependymomas: a population-based study. J Neurosurg Pediatr 15:243–249. doi:10.3171\u002F2014.9.PEDS1473\nAdams H, Avendaño J, Raza SM et al (2012) Prognostic factors and survival in primary malignant astrocytomas of the spinal cord: a population-based analysis from 1973 to 2007. Spine (Phila Pa 1976) 37:E727–E735. doi:10.1097\u002FBRS.0b013e31824584c0\nWong AP, Dahdaleh NS, Fessler RG et al (2013) Risk factors and long-term survival in adult patients with primary malignant spinal cord astrocytomas. J Neuro-Oncol 115:493–503. doi:10.1007\u002Fs11060-013-1296-y\nWolff B, Ng A, Roth D et al (2012) Pediatric high grade glioma of the spinal cord: results of the HIT-GBM database. J Neuro-Oncol 107:139–146. doi:10.1007\u002Fs11060-011-0718-y\nBenesch M, Weber-Mzell D, Gerber NU et al (2010) Ependymoma of the spinal cord in children and adolescents: a retrospective series from the HIT database. J Neurosurg Pediatr 6:137–144. doi:10.3171\u002F2010.5.PEDS09553\nFeldman WB, Clark AJ, Safaee M et al (2013) Tumor control after surgery for spinal myxopapillary ependymomas: distinct outcomes in adults versus children: a systematic review. J Neurosurg Spine 19:471–476. doi:10.3171\u002F2013.6.SPINE12927\nLam SK, Pan I-W, Harris DA et al (2015) Patient-, procedure-, and hospital-related risk factors of allogeneic and autologous blood transfusion in pediatric spinal fusion surgery in the United States. Spine (Phila Pa 1976) 40:560–569. doi:10.1097\u002FBRS.0000000000000816\nKhursheed N, Rumana M, Ramzan A et al (2011) Pediatric epidural tumors of the spine--experience of a decade from the Kashmir Valley. Pediatr Neurosurg 47:22–30. doi:10.1159\u002F000327142\nSafaee M, Oh MC, Mummaneni PV et al (2014) Surgical outcomes in spinal cord ependymomas and the importance of extent of resection in children and young adults. J Neurosurg Pediatr 13:393–399. doi:10.3171\u002F2013.12.PEDS13383",{"VOID":1218},"10.1007\u002Fs00381-017-3433-y","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00381-017-3433-y",[1221,1245,1260,1278,1293,1306,1321],{"id":1222,"sortIndex":32,"researcher":28,"roles":1223,"affiliations":1224,"properties":1242},"ce2b673d-9377-4995-a688-a521700e0740",[1061],[1225,1233],{"id":1226,"sortIndex":32,"affiliation":1227,"properties":28},"f36be92b-e445-44a4-8bb0-8bcbe8ec7e24",{"id":1226,"createTime":28,"updateTime":28,"relativeEntities":1228,"slug":28,"properties":1229,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1232,"statistic":28},[],{"title":1230},{"VI":1231},"Center for Neurosurgical Outcomes Research, Maxine Dunitz Neurosurgical Institute, Department of Neurosurgery, Cedars-Sinai Medical Center, Advanced Health Sciences Pavilion, Los Angeles, USA",[],{"id":1234,"sortIndex":40,"affiliation":1235,"properties":1241},"1b7af4ec-100e-4acf-bf55-5429aafff136",{"id":1234,"createTime":28,"updateTime":28,"relativeEntities":1236,"slug":28,"properties":1237,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1240,"statistic":28},[],{"title":1238},{"VI":1239},"Department of Surgery, University of Arizona College of Medicine, Tucson, USA",[],{},{"title":1243},{"VI":1244},"Faris Shweikeh",{"id":1246,"sortIndex":40,"researcher":28,"roles":1247,"affiliations":1248,"properties":1257},"3de67994-f8bb-4669-ba96-fad5e6b1eee9",[1061],[1249],{"id":1250,"sortIndex":32,"affiliation":1251,"properties":28},"db5e970a-1e99-432d-929a-2597e0832fac",{"id":1250,"createTime":28,"updateTime":28,"relativeEntities":1252,"slug":28,"properties":1253,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1256,"statistic":28},[],{"title":1254},{"VI":1255},"Department of Neurosurgery, University of North Carolina, Chapel Hill, USA",[],{"title":1258},{"VI":1259},"Carolyn Quinsey",{"id":1261,"sortIndex":123,"researcher":28,"roles":1262,"affiliations":1263,"properties":1275},"bd2eaa31-47c8-4512-87f2-69508834c58d",[1061],[1264],{"id":1265,"sortIndex":32,"affiliation":1266,"properties":1272},"bea23acf-cd0d-49e9-8069-5ff0f04ef745",{"id":1265,"createTime":28,"updateTime":28,"relativeEntities":1267,"slug":28,"properties":1268,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1271,"statistic":28},[],{"title":1269},{"VI":1270},"Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States",[],{"title":1273},{"VI":1274},"Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA",{"title":1276},{"VI":1277},"Roger Murayi",{"id":1279,"sortIndex":42,"researcher":28,"roles":1280,"affiliations":1281,"properties":1290},"73403b62-5cde-417f-b8ca-d6549fb43821",[1061],[1282],{"id":1283,"sortIndex":32,"affiliation":1284,"properties":28},"0a11a52e-84b5-4f9f-84a7-45489fd58c51",{"id":1283,"createTime":28,"updateTime":28,"relativeEntities":1285,"slug":28,"properties":1286,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1289,"statistic":28},[],{"title":1287},{"VI":1288},"David Geffen School of Medicine at UCLA, Los Angeles, USA",[],{"title":1291},{"VI":1292},"Ryan Randle",{"id":1294,"sortIndex":45,"researcher":28,"roles":1295,"affiliations":1296,"properties":1303},"4835ab0e-7e12-4a7c-ad2e-7842d7dbae06",[1061],[1297],{"id":1226,"sortIndex":32,"affiliation":1298,"properties":28},{"id":1226,"createTime":28,"updateTime":28,"relativeEntities":1299,"slug":28,"properties":1300,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1302,"statistic":28},[],{"title":1301},{"VI":1231},[],{"title":1304},{"VI":1305},"Miriam Nuño",{"id":1307,"sortIndex":46,"researcher":28,"roles":1308,"affiliations":1309,"properties":1318},"3f2b55e7-acfe-4ade-8840-4499a56781e8",[1061],[1310],{"id":1311,"sortIndex":32,"affiliation":1312,"properties":28},"9e92a95a-c60a-4e64-add6-722f0616f756",{"id":1311,"createTime":28,"updateTime":28,"relativeEntities":1313,"slug":28,"properties":1314,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1317,"statistic":28},[],{"title":1315},{"VI":1316},"Department of Neurosurgery, University of Southern California, Los Angeles, USA",[],{"title":1319},{"VI":1320},"Mark D. Krieger",{"id":1322,"sortIndex":48,"researcher":28,"roles":1323,"affiliations":1324,"properties":1331},"2d061bd7-cfde-4711-9464-074cd8796c33",[1061],[1325],{"id":1226,"sortIndex":32,"affiliation":1326,"properties":28},{"id":1226,"createTime":28,"updateTime":28,"relativeEntities":1327,"slug":28,"properties":1328,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1330,"statistic":28},[],{"title":1329},{"VI":1231},[],{"title":1332},{"VI":1333},"J. 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case of a 9-year-old-boy with a left frontal hydatid cyst is reported. The infection was transmitted by a dog, the final host and a companion of the child. Recovery without complications was accomplished after puncturing, systemic antihelminthic therapy using mebendazole and, finally, total removal of the cyst.",{"EN":1403},"Cerebral manifestation of hydatid disease in a child",{"VOID":1405},"Abada M, Galli U, Bousallah A, Lehmann G, Abassioun K (1977) Hydatid cysts of the brain. Clinical and surgical problems about [sic] 100 cases. Neurochirurgie 23:195–204\nAbassioun K, Rahmat M, Ameli N (1978) Computerized tomography in hydatid cyst of the brain. J Neurosurg 49:408–411\nAllgoyer H, Märlin M, Weinzierl M, Bircher J., Paumgartner G (1984) Mebendazol-Therapie d. Echinokokosse. Dtsch Med Wochenschr 109:1521–1524\nAnan A, Luiguez R (1977) Hydatidosis of the nervous system. Proceedings of the Xth International Congress of Neurology, Barcelona, Spain, New York, pp 254–260\nAssad F, Lins E (1984) Mykotisches Aneurysma d. A. cerebri media bei Echinokokkenbefall. Neurochirurgia 27:89–92\nAzidi D (1973) A propos de cystes hydatiques operés a Theheran\u002FIran. G Iran Med Council 2:127\nBagchi Ak. (1983) Infections and infestation of the cerebral nervous system in India. Neurosurg Rev 6:93–101\nBalakischran D, Natarajan M (1973) Hydatid cysts of the skull. J. Indian Med Assoc 61:88–91\nBala Subramaniam U, Rahanuiam PB, Ramamurthi B (1970) Hydatid disease of the nervous system. Indian J Neurol 18:92\nBanna M (1976) Arachnoid cysts on computerized tomography. AJR 127:979–982\nBrumner G, Reisner Th, Schnaberth G (1980) Primärer intracerebraler Befall durch Echinococcus cysticus. Nervenarzt 51:43–46\nCarea R, Dowling RE, Gvevara JA (1975) Surgical treatment of hydatid cysts of the central nervous system in pediatric age (Dowlings technique). Child's Brain 1:4–21\nFischer E (1955) Die parasitiven Erkrankungen des ZNS und seiner Hüllen. In: Scholz W (ed) Handbuch der Neuropathologie. Springer, Berlin Heidelberg, pp 372–412\nHaddad FS (1957) Hydatid disease of the brain. Some consideration [sic] of its recurrence. Arch Int Hydatid 16:445–447\nKon P (1983) Human echinococcus. Follow-up of 23 patients treated with mebendazole. Infection 11:17–21\nMohadjer M, Alimohammed A, Tarassali Y, Khadiw M, Mirr M (1986) Die Bedeutung der präoperativen CT-Diagnose von Echinokokkus-Zysten d. Gehirns. Neurochirugia 29:50–52\nPeters G (1970) Klinische Neuropathologie. Thieme, Stuttgart, p 121\nPorat S (1984) Hydatid cyst of the spine causing paraplegia. Spine 9:648–653\nRaja-Reddy D, Ayananada RB, Prabhakar V, Subramaniam MV (1972) Hydatid disease of the central nervous system. Indian J Surg 34:191\nRodriguez JC, Gutierroz RA, Valdes OD, Dorfsmann GF (1978) The role of computed axial tomography in the diagnosis and treatment of brain inflammatory and parasitic lesions: our experience in Mexico. Neuroradiology 16:458–461\nSpillane JD (ed) (1977) Tropical neurology. Oxford University Press, London\nTuncalp Özgen MD, Vural Bertan MD, Tülay Kansu MD, Sema Akalin MD (1984) Intrasellar hydatid cyst. J Neurosurg 60:647–648\nVasal PC, Sharmar UP, Agaraval RK (1978) Jugular foramen syndrome due to hydatid cyst. Indian J Neurol 26:74\nVengsarkar US, Abraham U (1965) Hydatid disease of the spine. 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In: Samuel Greenblatt H, Forcht Dagi T, Mel Epstein H (eds) A history of neurosurgery. Park Ridge, Illinois, pp 345–354\nOtto AW (1831) A compendium of human and comparative pathological anatomy. B. Fellowes, London\nVirchow R (1851) Über den Cretinismus, namentlich in Franken, und über pathologische Schädelformen. 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sarcoma (HS) of the central nervous system (CNS) is exceptionally rare in pediatric patients, historically associated with an exceptionally poor prognosis. Here, the authors present a novel case of protracted progression-free survival following surgical excision, radiotherapy and temozolomide. A 15-year-old Caucasian girl presented with a two-month history of headache, diplopia, vomiting, lethargy, weight loss and neurocognitive deterioration without gross neurological deficit on physical examination. Magnetic resonance imaging (MRI) of the brain identified a 5.8 × 4.7 × 4.0 cm lesion in the right frontal lobe with associated mass effect and no dissemination. Following two surgical procedures, gross total resection was achieved. Histology and immunohistochemistry confirmed HS, with strong CD163 staining. After focal radiotherapy with concomitant temozolomide, and a further seven cycles of temozolomide, the patient made an excellent recovery and is recurrence free without neurological deficit, 23 months following presentation. To the authors’ knowledge, this is the first incidence of a prolonged, functionally preserved and recurrence-free outcome following a diagnosis of HS within the CNS of a pediatric patient. We suggest early diagnosis prior to dissemination and complete surgical resection as an essential treatment goal in this rare disease.",{"EN":1622},"Primary cerebral histiocytic sarcoma in childhood: a case report of protracted survival and review of the literature",{"VOID":1624},"Favara BE, Feller AC, Pauli M, et al. (1997) Contemporary classification of histiocytic disorders. Med Pediatr Oncol 29:157–166. doi:10.1002\u002F(SICI)1096-911X(199709)29:3\u003C157::AID-MPO1>3.0.CO;2-C\nEgeler RM, Schmitz L, Sonneveld P, et al. (1995) Malignant histiocytosis: a reassessment of cases formerly classified as histiocytic neoplasms and review of the literature. Med Pediatr Oncol 25:1–7\nAlmefty RO, Tyree TL, Fusco DJ, et al. (2013) Primary histiocytic sarcoma of the brain mimicking cerebral abscess. J Neurosurg-Pediatr 12:251–257. doi:10.3171\u002F2013.6.PEDS12533\nCheuk W, Walford N, Lou J, et al. (2001) Primary histiocytic lymphoma of the central nervous system—a neoplasm frequently overshadowed by a prominent inflammatory component. Am J Surg Pathol 25:1372–1379. doi:10.1097\u002F00000478-200111000-00004\nGomi K, Tanaka M, Yoshida M, et al. (2012) Primary cerebellar histiocytic sarcoma in a 17-month-old girl case report. J Neurosurg-Pediatr 10:126–129. doi:10.3171\u002F2012.5.PEDS11270\nOrsey A, Paessler M, Lange BJ, Nichols KE (2008) Central nervous system juvenile xanthogranuloma with malignant transformation. Pediatr Blood Cancer 50:927–930. doi:10.1002\u002Fpbc.21252\nSun W, Nordberg ML, Fowler MR (2003) Histiocytic sarcoma involving the central nervous system—clinical, immunohistochemical, and molecular genetic studies of a case with review of the literature. Am J Surg Pathol 27:258–265. doi:10.1097\u002F00000478-200302000-00017\nTorres CF, Korones DN, Powers JM, Vadasz AG (1996) Primary leptomeningeal histiocytic lymphoma in a young child. Med Pediatr Oncol 27:547–550. doi:10.1002\u002F(SICI)1096-911X(199612)27:6\u003C547::AID-MPO7>3.0.CO;2-L\nO’Brien M (2010) Aids to the examination of the peripheral nervous system. Saunders\nStupp R, Mason WP, van den Bent MJ, et al. (2005) Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 352:987–996. doi:10.1056\u002FNEJMoa043330\nRawson J, Robinson A, Grogan P, Marshall S (2012) A rare neoplasm masquerading as an infectious process. Neurology 78(Meeting Abstracts 1):P03.143. doi:10.1212\u002FWNL.78.1_MeetingAbstracts.P03.143\nVos JA, Abbondanzo SL, Barekman CL, Andriko JW, Miettinen M, Aguilera NS (2005) Histiocytic sarcoma: a study of five cases including the histiocyte marker CD163. Mod Pathol 18:693–704\nPerez-Ruiz E, Delgado M, Sanz A, et al. (2013) Primary leptomeningeal histiocytic sarcoma in a patient with a good outcome: a case report and review of the literature. J Med Case Rep 7:127–127. doi: 10.1186\u002F1752-1947-7-127\nBell SL, Hanzely Z, Alakandy LM, et al. (2012) Primary meningeal histiocytic sarcoma: a report of two unusual cases. Neuropathol Appl Neurobiol 38:111–114. doi:10.1111\u002Fj.1365-2990.2011.01205.x\nWu W, Sayit AT, Vinters HV, et al. (2013) Primary central nervous system histiocytic sarcoma presenting as a postradiation sarcoma: case report and literature review. Hum Pathol 44:1177–1183. doi:10.1016\u002Fj.humpath.2012.11.002\nCao M, Eshoa C, Schultz C, et al. (2007) Primary central nervous system histiocytic sarcoma with relapse to mediastinum—a case report and review of the literature. 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ventriculomegaly (VM) refers to the enlargement of the cerebral ventricles in utero. It is associated with the postnatal diagnosis of hydrocephalus. VM is clinically diagnosed on ultrasound and is defined as an atrial diameter greater than 10 mm. Because of the anatomic detailed seen with advanced imaging, VM is often further characterized by fetal magnetic resonance imaging (MRI). Fetal VM is a heterogeneous condition with various etiologies and a wide range of neurodevelopmental outcomes. These outcomes are heavily dependent on the presence or absence of associated anomalies and the direct cause of the ventriculomegaly rather than on the absolute degree of VM. In this review article, we discuss diagnosis, work-up, counseling, and management strategies as they relate to fetal VM. We then describe imaging-based research efforts aimed at using prenatal data to predict postnatal outcome. Finally, we review the early experience with fetal therapy such as in utero shunting, as well as the advances in prenatal diagnosis and fetal surgery that may begin to address the limitations of previous therapeutic efforts.",{"EN":1896},"Fetal ventriculomegaly: Diagnosis, treatment, and future directions",{"VOID":1898},"Edwards JH (1958) Congenital malformations of the central nervous system in Scotland. Br J Prev Soc Med 12:115–130\nLaurence KM, Carter CO, David PA (1968) Major central nervous system malformations in South Wales. I. Incidence, local variations and geographical factors. Br J Prev Soc Med 22:146–160\nAlmog B, Gamzu R, Achiron R et al (2003) Fetal lateral ventricular width: what should be its upper limit? A prospective cohort study and reanalysis of the current and previous data. J Ultrasound Med 22:39–43\nCardoza JD, Goldstein RB, Filly RA (1988) Exclusion of fetal ventriculomegaly with a single measurement: the width of the lateral ventricular atrium. Radiology 169:711–714. doi:10.1148\u002Fradiology.169.3.3055034\nGoynumer G, Yayla M, Arisoy R, Turkmen O (2014) The criterion value of fetal cerebral lateral ventricular atrium width for diagnosis of ventriculomegaly. Clin Exp Obstet Gynecol 41:67–71\nMcKechnie L, Vasudevan C, Levene M (2012) Neonatal outcome of congenital ventriculomegaly. Semin Fetal Neonatal Med 17:301–307. doi:10.1016\u002Fj.siny.2012.06.001\nGriffiths PD, Reeves MJ, Morris JE et al (2010) A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging. AJNR Am J Neuroradiol 31:106–111. doi:10.3174\u002Fajnr.A1767\nNorton M (2016) Fetal cerebral ventriculomegaly. In: UpToDate\nBruner JP, Davis G, Tulipan N (2006) Intrauterine shunt for obstructive hydrocephalus—still not ready. Fetal Diagn Ther 21:532–539. doi:10.1159\u002F000095668\nWang K-C, Lee JY, Kim S-K et al (2011) Fetal ventriculomegaly: postnatal management. Childs Nerv Syst 27:1571–1573. doi:10.1007\u002Fs00381-011-1556-0\nVon Koch CS, Gupta N, Sutton LN, Sun PP (2003) In utero surgery for hydrocephalus. Childs Nerv Syst 19:574–586. doi:10.1007\u002Fs00381-003-0775-4\nPilu G, Reece EA, Goldstein I et al (1989) Sonographic evaluation of the normal developmental anatomy of the fetal cerebral ventricles: II. The atria. Obstet Gynecol 73:250–256\nMelchiorre K, Bhide A, Gika AD et al (2009) Counseling in isolated mild fetal ventriculomegaly. Ultrasound Obstet Gynecol 34:212–224. doi:10.1002\u002Fuog.7307\nSadan S, Malinger G, Schweiger A et al (2007) Neuropsychological outcome of children with asymmetric ventricles or unilateral mild ventriculomegaly identified in utero. BJOG 114:596–602. doi:10.1111\u002Fj.1471-0528.2007.01301.x\nAtad-Rapoport M, Schweiger A, Lev D et al (2015) Neuropsychological follow-up at school age of children with asymmetric ventricles or unilateral ventriculomegaly identified in utero. BJOG 122:932–938. doi:10.1111\u002F1471-0528.12976\nDurfee SM, Kim FM, Benson CB (2001) Postnatal outcome of fetuses with the prenatal diagnosis of asymmetric hydrocephalus. J Ultrasound Med 20:263–268\nGaglioti P, Oberto M, Todros T (2009) The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes. Prenat Diagn 29:381–388. doi:10.1002\u002Fpd.2195\nKandula T, Fahey M, Chalmers R et al (2015) Isolated ventriculomegaly on prenatal ultrasound: what does fetal MRI add? J Med Imaging Radiat Oncol 59:154–162. doi:10.1111\u002F1754-9485.12287\nHannon T, Tennant PWG, Rankin J, Robson SC (2012) Epidemiology, natural history, progression, and postnatal outcome of severe fetal ventriculomegaly. Obstet Gynecol 120:1345–1353. doi:10.1097\u002FAOG.0b013e3182732b53\nGaglioti P, Danelon D, Bontempo S et al (2005) Fetal cerebral ventriculomegaly: outcome in 176 cases. Ultrasound Obstet Gynecol 25:372–377. doi:10.1002\u002Fuog.1857\nSethna F, Tennant PWG, Rankin J, Robson SC (2011) Prevalence, natural history, and clinical outcome of mild to moderate ventriculomegaly. Obstet Gynecol 117:867–876. doi:10.1097\u002FAOG.0b013e3182117471\nPagani G, Thilaganathan B, Prefumo F (2014) Neurodevelopmental outcome in isolated mild fetal ventriculomegaly: systematic review and meta-analysis. Ultrasound Obstet Gynecol 44:254–260. doi:10.1002\u002Fuog.13364\nCardoen L, De Catte L, Demaerel P et al (2011) The role of magnetic resonance imaging in the diagnostic work-up of fetal ventriculomegaly. Facts Views Vis ObGyn 3:159–163\nPier DB, Levine D, Kataoka ML et al (2011) Magnetic resonance volumetric assessments of brains in fetuses with ventriculomegaly correlated to outcomes. J Ultrasound Med 30:595–603\nParazzini C, Righini A, Doneda C et al (2012) Is fetal magnetic resonance imaging indicated when ultrasound isolated mild ventriculomegaly is present in pregnancies with no risk factors? Prenat Diagn 32:752–757. doi:10.1002\u002Fpd.3896\nBenacerraf BR, Shipp TD, Bromley B, Levine D (2007) What does magnetic resonance imaging add to the prenatal sonographic diagnosis of ventriculomegaly? J Ultrasound Med 26:1513–1522\nSalomon LJ, Ouahba J, Delezoide A-L et al (2006) Third-trimester fetal MRI in isolated 10- to 12-mm ventriculomegaly: is it worth it? BJOG 113:942–947. doi:10.1111\u002Fj.1471-0528.2006.01003.x\nManganaro L, Savelli S, Francioso A et al (2009) Role of fetal MRI in the diagnosis of cerebral ventriculomegaly assessed by ultrasonography. Radiol Med 114:1013–1023. doi:10.1007\u002Fs11547-009-0434-2\nMorris JE, Rickard S, Paley MNJ et al (2007) The value of in-utero magnetic resonance imaging in ultrasound diagnosed foetal isolated cerebral ventriculomegaly. Clin Radiol 62:140–144. doi:10.1016\u002Fj.crad.2006.06.016\nKelly EN, Allen VM, Seaward G et al (2001) Mild ventriculomegaly in the fetus, natural history, associated findings and outcome of isolated mild ventriculomegaly: a literature review. Prenat Diagn 21:697–700\nVergani P, Locatelli A, Strobelt N et al (1998) Clinical outcome of mild fetal ventriculomegaly. Am J Obstet Gynecol 178:218–222\nParilla BV, Endres LK, Dinsmoor MJ, Curran L (2006) In utero progression of mild fetal ventriculomegaly. Int J Gynaecol Obstet 93:106–109. doi:10.1016\u002Fj.ijgo.2006.01.026\nMelchiorre K, Liberati M, Celentano C et al (2009) Neurological outcome following isolated 10-12 mm fetal ventriculomegaly. Arch Dis Child Fetal Neonatal Ed 94:F311–F312. doi:10.1136\u002Fadc.2007.134312\nBeeghly M, Ware J, Soul J et al (2010) Neurodevelopmental outcome of fetuses referred for ventriculomegaly. Ultrasound Obstet Gynecol 35:405–416. doi:10.1002\u002Fuog.7554\nKutuk MS, Ozgun MT, Uludag S et al (2013) Postnatal outcome of isolated, nonprogressive, mild borderline fetal ventriculomegaly. Childs Nerv Syst 29:803–808. doi:10.1007\u002Fs00381-013-2020-0\nDevaseelan P, Cardwell C, Bell B, Ong S (2010) Prognosis of isolated mild to moderate fetal cerebral ventriculomegaly: a systematic review. J Perinat Med 38:401–409. doi:10.1515\u002FJPM.2010.048\nLaskin MD, Kingdom J, Toi A et al (2005) Perinatal and neurodevelopmental outcome with isolated fetal ventriculomegaly: a systematic review. J Matern Fetal Neonatal Med 18:289–298. doi:10.1080\u002F14767050500329775\nBreeze ACG, Alexander PMA, Murdoch EM et al (2007) Obstetric and neonatal outcomes in severe fetal ventriculomegaly. 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ependymomas in children have high rates of recurrence. Salvage therapy typically includes repeat resection, possibly chemotherapy, and re-irradiation. Stereotactic radiosurgery has been used for re-irradiation. It offers the theoretical advantages of delivering a high dose of radiation to a small target, providing a maximum dose to the tumor while avoiding surrounding critical brain structures and previously irradiated tissue. Few reports in the literature describe this technique, with mixed, but not often successful, outcomes.",{"EN":2151},"The role of stereotactic radiotherapy in the management of ependymomas",{"VOID":2153},"Aggarwal R, Yeung D, Kumar P, Muhlbauer M, Kun LE (1997) Efficacy and feasibility of stereotactic radiosurgery in the primary management of unfavorable pediatric ependymoma. Radiother Oncol 43:269–273\nDuffner PK, Krischer JP, Sanford RA et al (1998) Prognostic factors in infants and very young children with intracranial ependymomas. Pediatr Neurosurg 28:215–222\nEndo H, Kumabe T, Jokura H, Shirane R, Tominaga T (2004) Case report: stereotactic radiosurgery for nodular dissemination of anaplastic ependymoma. Acta Neurochir 146:291–298\nForeman NK, Love S, Thorne R (1996) Intracranial ependymomas: analysis os prognostic factors in a population-based series. Pediatr Neurosurg 24:119–125\nGrabb PA, Lunsford LD, Albright AL, Kondziolka D, Flickinger JC (1996) Stereotactic radiosurgery for glial neoplasms of childhood. Neurosurgery 38(4):696–702\nHirato M, Nakamura M, Inoue HK, Ohye C, Hirato J, Shibazaki T, Andou Y (1995) Gamma knife radiosurgery for the treatment of brainstem tumors. Stereotact Funct Neurosurg 64(Suppl 1):32–41\nHodgson DC, Goumnerova LC, Loeffler JS, Dutton S, Black PM, Alexander E III, Xu R, Kooy H, Silver B, Tarbell N (2001) Radiosurgery in the management of pediatric brain tumors. Int J Radiation Oncology Biol Phys 50(4):929–935\nHorn B, Heideman R, Geyer R, Pollack I, Packer R, Goldwein J, Tomita T, Schomberg P, Ater J, Luchtman-Jones L, Rivlin K, Lamborn K, Prados M, Bollen A, Berger M, Dahl G, McNeil E, Patterson K, Shaw D, Kubalik M, Russo C (1999) A multi-institutional retrospective study of intracranial ependymomas in children: identification of risk factors. J Pediatr Hematol Oncol 21:203–211\nJawahar A, Kondiolka D, Flickinger JC, Lunsford LD (1999) Adjuvant stereotactic radiosurgery for anaplastic ependymoma. Stereotact Funct Neurosurg 73(1–4):23–30\nKano H, Niranjan A, Kondziolka D, Flickinger JC, Lunsford LD (2009) Outcome predictors for intracranial ependymoma radiosurgery. Neurosurg 64:279–288\nLiu AK, Foreman NK, Gaspar LE, Trinidad E, Handler MH (2009) Maximally safe resection followed by hypofractionated re-irradiation for locally recurrent ependymoma in children. Pediatr Blood Cancer 00:1–4\nLo SS, Chang EL, Sloan AE (2006) Role of stereotactic radiosurgery and fractionated stereotactic radiotherapy in the management of intracranial ependymoma. Expert Rev Neurotherapeutics 6(4):501–507\nLo SS, Abdulrahman R, DesRosiers PM, Fakiris AJ, Witt TC, Worth RM, Dittmer PH, DesRosiers CM, Frost S, Timmerman RD (2006) The role of gamma knife radiosurgery in the management of unresectable gross disease or gross residual disease after surgery in ependymoma. Journal of Neuro-Oncology 79:51–56\nLoeffler JS, Rossitch E, Siddon R, Moore MR, Rockoff MA, Alexander E (1990) Role of stereotactic radiosurgery with a linear accelerator in treatment of intracranial arteriovenous malformations and tumors in children. Pediatrics 85:774–782\nMansur DB, Drzymala RE, Rich KM, Klein EE, Simpson JR (2004) The efficacy of stereotactic radiosurgery in the management of intracranial ependymoma. Journal of Neuro-Oncology 66:187–190\nMerchant TE (2002) Current management of childhood ependymoma. Oncology 6(5):629–642\nMerchant TE, Boop FA, Kun LE, Sanford RA (2008) A retrospective study of surgery and reirradiation for recurrent ependymoma. Int J Radiation Oncology Biol Phys 71(1):87–97\nNazar GB, Hoffman HJ, Becker LE, Jenkin D, Humphreys RP, Hendrick EB (1990) Intratentorial ependymomas in childhood: prognostic factors and treatment. J Neurosurg 72:408–417\nNeedle MN, Goldwein JW, Grass J, Cnaan A, Bergman I, Molloy P, Sutton L, Zhao H, Garvin JH, Phillips PC (1997) Adjuvant chemotherapy for the treatment of intracranial ependymoma of childhood. Cancer 80:341–347\nPerilongo G, Massimino M, Sotti G, Belfontali T, Masiero L, Rigobello L, Garre L, Carli M, Lombardi F, Solero C, Sainati L, Canale V, del Prever AB, Biangaspero F, Andreussi L, Massa C, Madon E (1997) Analysies of prognostic factors in a retrospective review of 92 children with ependymoma: Italian Pediatric Neurooncology Group. Med Pediatr Oncol 29:79–85\nPollack IF, Gerszten PC, Martinez AJ, Lo KH, Shultz B, Albright AL, Janosky J, Deutsch M (1995) Intracranial ependymomas of childhood: long-term outcome and prognostic factors. Neurosurgery 37:655–666\nRobertson PL, Zeltzer P, Boyett JM, Rorke LB, Allen JC, Geyer JR, Stanley P, Li H, Albright AL, McGuire-Cullen P, Finlay JL, Stevens KR, Milstein JM, Packer RJ, Wisoff J (1998) Survival and prognostic factors following radiation therapy and chemotherapy for ependymomas in children: a report of the Children’s Cancer Group. J Neurosurg 88:695–703\nRousseau P, Habrand J, Sarrazin D, Kalifa C, Terrier-Lacombe MJ, Rekacewicz C, Rey A (1994) Treatment of intracranial ependymomas of children: review of a 15-year experience. Int J Radiat Biol Phys 28:381–386\nStafford SL, Pollock BE, Foote RL, Gorman DA, Nelson DF, Schomberg PJ (2000) Stereotactic radiosurgery for recurrent ependymoma. Cancer 88(4):870–875\nSutton LN, Goldwein J, Perilongo G, Lang B, Schut L, Rorke L (1990) Prognostic factors in childhood ependymomas. Pediatr Neurosurg 16:57–65\nWeprin BE, Hall WA, Cho KH, Sperduto PW, Gerbi BJ, Moertel C (1996) Stereotactic radiosurgery in pediatric patients. Pediatr Neurol 15:193–199",{"VOID":2155},"10.1007\u002Fs00381-009-0879-6","2025-01-25T12:21:42.798+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00381-009-0879-6",[2159,2191],{"id":2160,"sortIndex":32,"researcher":28,"roles":2161,"affiliations":2162,"properties":2189},"17b70b40-325d-48b4-889c-9e610ee3d6aa",[1061],[2163,2171,2180],{"id":2164,"sortIndex":32,"affiliation":2165,"properties":28},"296ad30c-ca6f-485a-b907-91f5c909b4c2",{"id":2164,"createTime":28,"updateTime":28,"relativeEntities":2166,"slug":28,"properties":2167,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2170,"statistic":28},[],{"title":2168},{"VI":2169},"Division of Neurosurgery, Childrens Hospital Los Angeles, Los Angeles, USA",[],{"id":2172,"sortIndex":40,"affiliation":2173,"properties":2179},"a250ab68-3e73-4095-8a31-a29d3fde2a3a",{"id":2172,"createTime":28,"updateTime":28,"relativeEntities":2174,"slug":28,"properties":2175,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2178,"statistic":28},[],{"title":2176},{"VI":2177},"Department of Neurological Surgery, Keck School of Medicine, University of Southern California, Los Angeles, USA",[],{},{"id":2181,"sortIndex":123,"affiliation":2182,"properties":2188},"ce52d01f-2a86-46a9-9a3c-c1b4503d2a26",{"id":2181,"createTime":28,"updateTime":28,"relativeEntities":2183,"slug":28,"properties":2184,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2187,"statistic":28},[],{"title":2185},{"VI":2186},"Division of Pediatric Neurosurgery, Los Angeles, USA",[],{},{"title":2190},{"VI":1320},{"id":2192,"sortIndex":40,"researcher":28,"roles":2193,"affiliations":2194,"properties":2208},"64183060-57ac-4a92-814d-2480fd638cbe",[1061],[2195,2201],{"id":2164,"sortIndex":32,"affiliation":2196,"properties":28},{"id":2164,"createTime":28,"updateTime":28,"relativeEntities":2197,"slug":28,"properties":2198,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2200,"statistic":28},[],{"title":2199},{"VI":2169},[],{"id":2172,"sortIndex":40,"affiliation":2202,"properties":2207},{"id":2172,"createTime":28,"updateTime":28,"relativeEntities":2203,"slug":28,"properties":2204,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2206,"statistic":28},[],{"title":2205},{"VI":2177},[],{},{"title":2209},{"VI":2210},"J. 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anomalies most frequently present at birth or in early childhood, and the craniofacial region is the most common site of involvement. A long history of misleading nomenclature born of confusion about the presentation and natural history of various vascular anomalies has made appropriate diagnosis difficult. The present article emphasizes the importance of clarity of nomenclature for proper diagnosis, both clinically and radiographically, to guide appropriate therapy. In addition, updates on clinical concepts, imaging, and treatment strategies will be discussed. Pediatric vascular anomalies can be divided into two broad categories: vascular tumors and vascular malformations. This biologic classification is based on differences in natural history, cellular turnover, and histology. An updated classification was introduced in 1996 by the International Society for the Study of Vascular Anomalies (ISSVA) to include infantile hemangioma variants, other benign vascular tumors, and combined lesions. Widespread confusion propagated throughout the literature and in clinical practice stems from the continued improper use of many of the terms used to describe vascular tumors and malformations ignoring their pathophysiology. This leads to errors in diagnosis and the dissemination of misinformation to patients and clinicians. Certain terms should be abandoned for more appropriate terms. The clinical presentation usually identifies what general type of vascular anomaly is present, either vascular tumor or vascular malformation. Imaging provides crucial information about the initial diagnosis and aids in follow-up. Adoption and use of uniform nomenclature in the ISSVA classification system is the first vital step in correct diagnosis and treatment of often complicated vascular tumors and vascular malformations. A multidisciplinary team approach is necessary to provide optimal care for patients, and the necessity for specialists in all areas to communicate using standardized terminology cannot be overemphasized.",{"EN":2279},"Update on pediatric extracranial vascular anomalies of the head and neck",{"EN":2281},"",{"VOID":2283},"Werner J, Dünne A-A, Folz BJ, Rochels R, Bien S, Ramaswamy S, Lipper BM (2001) Current concepts in the classification, diagnosis and treatment of hemangiomas and vascular malformations of the head and neck. Eur Arch Otorhinolaryngol 258:141–149\nMulliken JB, Glowacki J (1982) Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg 69(3):412–422\nEnjolras O, Mulliken JB (1997) Vascular tumors and vascular malformations (new issues). Adv Dermatol 13:375–423\nDubois J, Garel L (1999) Imaging and therapeutic approach of hemangiomas and vascular malformations in the pediatric age group. 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