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We report a case of postoperative isolated bile duct leakage managed successfully by combination therapy of percutaneous transhepatic portal vein embolization (PTPE) and bile duct ablation with ethanol. A 61-year-old man diagnosed with hepatocellular carcinoma underwent partial hepatectomy. On postoperative day 1, bile leakage was detected at the drainage tube. Simple drainage treatment did not improve the situation. He was diagnosed with isolated bile leakage based on fistulogram from the drainage tube that showed the bile duct at segments V and VIII but not the common bile duct. A volume of drainage fluid of 200 mL\u002Fday was observed. Combination therapy with PTPE and bile duct ablation with ethanol was planned. After the percutaneous transhepatic cholangiography, the drainage tube was inserted into the bile duct, and PTPE was performed to segments V and VIII. The amount of drainage fluid decreased, and bile duct ablation with ethanol was performed to the isolated bile duct. No complication was found following combination therapy. In this case, we successfully treated a patient with isolated bile leakage by combination therapy with PTPE and bile duct ablation.",{"EN":74},"Successful treatment of isolated bile leakage after hepatectomy combination therapy with percutaneous transhepatic portal embolization and bile duct ablation with ethanol: a case report",{"VOID":76},"[\"8504110721514802188\"]",{"VOID":78},"10.1186\u002Fs40792-018-0463-y","PUBLICATION","VERIFIED","2024-05-05T04:12:41.051+00:00","Auto 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Prospective evaluation of the International Study Group for Liver Surgery definition of bile leak after a liver resection and the role of routine operative drainage: an international multicentre study. HPB (Oxford). 2015;17:46–51.","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS1365182X15311655",{"doi":291},"10.1111\u002Fhpb.12322",{"id":293,"text":294,"url":295,"identifiers":296},"701182f3-bfa7-4406-be5d-fdebaad5eb83","Kyoden Y, Imamura H, Sano K, Beck Y, Sugawara Y, Kokudo N, et al. Value of prophylactic abdominal drainage in 1269 consecutive cases of elective liver resection. J Hepatobiliary Pancreat Sci. 2010;17:186–92.","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1007\u002Fs00534-009-0161-z",{"doi":297},"10.1007\u002Fs00534-009-0161-z",{"id":299,"text":300,"url":301,"identifiers":302},"4c68646b-0035-4279-8000-0006b275d4fa","Yang T, Zhang J, Lu JH, Yang GS, Wu MC, Yu WF. 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J Hepatobiliary Pancreat Sci. 2017;24:33–41.",{"doi":303},{"id":18,"text":311,"url":18,"identifiers":312},"Capussotti L, Ferrero A, Vigano L, Sgotto E, Muratore A, Polastri R. Bile leakage and liver resection: where is the risk? Arch Surg. 2006;141:690–4. discussion 695",{},{"id":299,"text":314,"url":301,"identifiers":315},"Erdogan D, Busch OR, van Delden OM, Rauws EA, Gouma DJ, van Gulik TM. Incidence and management of bile leakage after partial liver resection. Dig Surg. 2008;25:60–6.",{"doi":303},{"id":299,"text":317,"url":301,"identifiers":318},"Ishii H, Ochiai T, Murayama Y, Komatsu S, Shiozaki A, Kuriu Y, et al. Risk factors and management of postoperative bile leakage after hepatectomy without bilioenteric anastomosis. Dig Surg. 2011;28:198–204.",{"doi":303},{"id":299,"text":320,"url":301,"identifiers":321},"Nagano Y, Togo S, Tanaka K, Masui H, Endo I, Sekido H, et al. Risk factors and management of bile leakage after hepatic resection. World J Surg. 2003;27:695–8.",{"doi":303},{"id":323,"text":324,"url":325,"identifiers":326},"9c66bdc4-df52-415f-9f67-ab005e55c76b","Koch M, Garden OJ, Padbury R, Rahbari NN, Adam R, Capussotti L, et al. Bile leakage after hepatobiliary and pancreatic surgery: a definition and grading of severity by the International Study Group of Liver Surgery. Surgery. 2011;149:680–8.","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0039606010006781",{"doi":327},"10.1016\u002Fj.surg.2010.12.002",{"id":299,"text":329,"url":301,"identifiers":330},"Itoh S, Yoshizumi T, Shirabe K, Kimura K, Okabe H, Harimoto N, et al. Functional remnant liver assessment predicts liver-related morbidity after hepatic resection in patients with hepatocellular carcinoma. Hepatol Res. 2017;47:398–404.",{"doi":303},{"id":299,"text":332,"url":301,"identifiers":333},"Fukuhisa H, Sakoda M, Hiwatashi K, Iino S, Minami K, Hashiguchi M, et al. Surgical treatment for the excluded bile leakage from Spiegel lobe after right hemihepatectomy: a case report. Int J Surg Case Rep. 2017;39:159–63.",{"doi":303},{"id":299,"text":335,"url":301,"identifiers":336},"Sakamoto K, Tamesa T, Yukio T, Tokuhisa Y, Maeda Y, Oka M. Risk factors and managements of bile leakage after hepatectomy. World J Surg. 2016;40:182–9.",{"doi":303},{"id":299,"text":338,"url":301,"identifiers":339},"Woo S, Chung JW, Hur S, Joo SM, Kim HC, Jae HJ, et al. Liver abscess after transarterial chemoembolization in patients with bilioenteric anastomosis: frequency and risk factors. AJR Am J Roentgenol. 2013;200:1370–7.",{"doi":303},{"id":341,"text":342,"url":343,"identifiers":344},"f35fbd4f-f5d2-4bd3-ad9a-e8638e136275","Sadakari Y, Miyoshi A, Ohtsuka T, Kohya N, Takahashi T, Matsumoto K, et al. Percutaneous transhepatic portal embolization for persistent bile leakage after hepatic resection: report of a case. 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J Gastroenterol Hepatol. 2002;17:807–10.",{"doi":303},{"id":299,"text":356,"url":301,"identifiers":357},"Sakaguchi T, Shibasaki Y, Morita Y, Oishi K, Suzuki A, Fukumoto K, et al. Postoperative bile leakage managed by interventional intrabiliary ethanol ablation. Hepatogastroenterology. 2011;58:157–60.",{"doi":303},{"id":299,"text":359,"url":301,"identifiers":360},"Shimizu T, Yoshida H, Mamada Y, Taniai N, Matsumoto S, Mizuguchi Y, et al. Postoperative bile leakage managed successfully by intrahepatic biliary ablation with ethanol. World J Gastroenterol. 2006;12:3450–2.",{"doi":303},{"id":299,"text":362,"url":301,"identifiers":363},"Kataoka M, Ooeda Y, Yoshioka S, Wakatsuki K, Tonooka T, Kawamoto J, et al. Percutaneous transhepatic ethanol ablation for postoperative bile leakage after a hepatectomy. Hepatogastroenterology. 2011;58:988–91.",{"doi":303},{"id":299,"text":365,"url":301,"identifiers":366},"Kyokane T, Nagino M, Oda K, Nimura Y. An experimental study of selective intrahepatic biliary ablation with ethanol. J Surg Res. 2001;96:188–96.",{"doi":303},{"id":299,"text":368,"url":301,"identifiers":369},"Ikeda A, Noda T, Hatano H, Takata A, Hirota M, Oshima K, et al. A case of intractable bile leakage after surgery for gallbladder cancer successfully treated by transcatheter arterial embolization. Gan To Kagaku Ryoho. 2015;42:1734–6.",{"doi":303},false,{"id":372,"createTime":373,"updateTime":374,"relativeEntities":375,"slug":376,"properties":377,"entityType":79,"verifyStatus":80,"verifyTime":388,"verifyNote":82,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":389,"fullTextUrl":18,"authors":390,"publicationType":243,"publisherRelationship":436,"citationCount":18,"citationInfo":18,"publishDate":471,"publishYear":472,"citationAnalyzeStatus":473,"lastCitationAnalyze":18,"indexDatabases":474,"openAccess":18,"references":18,"isForceReanalyzing":370},"d00801e8-a5ea-46ab-8155-5dda17546ac8","2023-12-07T11:39:05.823+00:00","2026-07-17T22:04:51.417+00:00",[],"A-novel-reconstruction-technique-of-a-tracheal-defect-in-the-emergent-setting-using-a-thymus-flap-in-a-patient-with-tracheoinnominate-artery-fistula",{"abstract":378,"title":380,"gsPaper":382,"references":384,"doi":386},{"EN":379},"There is a very high mortality associated with a tracheoinnominate artery fistula; however, when patients survive, they often require reconstruction of the eroded tracheal defect after the bleeding has been controlled. This is the case of an 83-year-old male with a tracheoinnominate artery fistula who was stabilized in the operating room and underwent repair of his trachea. A novel technique of using the thymus gland as a pedicled flap to repair a large tracheal defect was executed after achieving hemostasis. The patient’s defect was repaired successfully following control of the fistula. We have shown that the thymus gland can be used successfully as a pedicled flap for repair of a tracheal defect in the setting of a tracheoinnominate artery fistula.",{"EN":381},"A novel reconstruction technique of a tracheal defect in the emergent setting using a thymus flap in a patient with tracheoinnominate artery fistula",{"VOID":383},"[\"14475285457170695793\"]",{"VOID":385},"Menen RS, Pak JJ, Dowell MA, Patel AR, Ashiku SK, Velotta JB. Treatment of tracheoinnominate fistula with ligation of the innominate artery: a case report. Perm J. 2016;20(3).\nGrant CA, Dempsey G, Harrison J, Jones T. Tracheo-innominate artery fistula after percutaneous tracheostomy: three case reports and a clinical review. Br J Anaesth. 2005;96(1):127–31.\nReger B, Neu R, Hofmann HS, Ried M. High mortality in patients with tracheoarterial fistulas: clinical experience and treatment recommendations. Interact Cardiovasc Thorac Surg. 2017;26(1):12–7.\nUdelsman BV, Eaton J, Muniappan A, Morse CR, Wright CD, Mathisen DJ. Repair of large airway defects with bioprosthetic materials. J Thorac Cardiovasc Surg. 2016;152(5):1388–97.\nAbouarab AA, Elsayed HH, Elkhayat H, Mostafa A, Cleveland DC, El Nori A. Current solutions for long-segment tracheal reconstruction. Ann Thorac Cardiovasc Surg. 2017:ra-16.\nIodice F, Brancaccio G, Lauri A, Di Donato R. Preventive ligation of the innominate artery in patients with neuromuscular disorders. Eur J Cardiothorac Surg. 2007;31(4):747–9.\nPalchik E, Bakken AM, Saad N, Saad WA, Davies MG. Endovascular treatment of tracheoinnominate artery fistula: a case report. Vasc Endovasc Surg. 2007;41(3):258–61.\nAhn HY, Son BS, Kim DH. Recurrent tracheoinnominate artery fistula due to stent graft fracture. Eur J Pediatr surg Rep. 2015;3(01):012–4.\nShimizu K, Nagashima T, Ohtaki Y, Takeyoshi I. Novel repair of a defect in the cervical trachea with a thymus pedicle flap. J Thorac Cardiovasc Surg. 2014;147(6):1988–90.\nAnderson M, Grucela A. Toxic megacolon. Semin Colon Rectal Surg. 2019;30(3):100691 WB Saunders.",{"VOID":387},"10.1186\u002Fs40792-019-0763-x","2024-06-25T04:29:54.620+00:00","https:\u002F\u002Fsurgicalcasereports.springeropen.com\u002Farticles\u002F10.1186\u002Fs40792-019-0763-x",[391,408,423],{"id":392,"sortIndex":19,"researcher":18,"roles":393,"affiliations":394,"properties":403,"displayName":405,"givenName":18,"familyName":18},"da5e54c6-ed7c-496a-9fb0-659271c0eda5",[88],[395],{"id":396,"sortIndex":19,"affiliation":397,"properties":18},"21ace375-7c1b-49a7-80dd-8f7f311e0d15",{"id":396,"createTime":18,"updateTime":18,"relativeEntities":398,"slug":18,"properties":399,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":402,"statistic":18},[],{"title":400},{"VI":401},"Department of Surgery, Icahn School of Medicine at Mount Sinai South Nassau, Oceanside, USA",[],{"title":404,"gsAuthor":406},{"VI":405},"Tyler B. Draeger",{"VOID":407},"[\"tzWTAUMAAAAJ\"]",{"id":409,"sortIndex":55,"researcher":18,"roles":410,"affiliations":411,"properties":420,"displayName":422,"givenName":18,"familyName":18},"40c115ed-0e7d-4c91-a873-5a0303904ddf",[88],[412],{"id":413,"sortIndex":19,"affiliation":414,"properties":18},"2b8864f0-c1b6-41a8-8071-cd426bd063c2",{"id":413,"createTime":18,"updateTime":18,"relativeEntities":415,"slug":18,"properties":416,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":419,"statistic":18},[],{"title":417},{"VI":418},"Division of Cardiothoracic Surgery, Department of Surgery, Icahn School of Medicine at Mount Sinai South Nassau, Oceanside, USA",[],{"title":421},{"VI":422},"Shahriyour K. Andaz",{"id":424,"sortIndex":57,"researcher":18,"roles":425,"affiliations":426,"properties":433,"displayName":435,"givenName":18,"familyName":18},"311642be-bbcc-4b44-9e4f-db3f7bfc027d",[88],[427],{"id":413,"sortIndex":19,"affiliation":428,"properties":18},{"id":413,"createTime":18,"updateTime":18,"relativeEntities":429,"slug":18,"properties":430,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":432,"statistic":18},[],{"title":431},{"VI":418},[],{"title":434},{"VI":435},"Vanessa R. Gibson",{"url":389,"publisher":437,"properties":466},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":438,"slug":10,"properties":439,"entityType":16,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":19,"subjectFields":442,"manageAffiliations":447,"indexDatabases":453,"url":18,"thumbnailPath":18,"statistic":461,"gsStatistic":18,"type":18,"analyzePriority":18},[],{"title":440,"eissn":441},{"EN":13},{"VOID":15},[443],{"id":22,"createTime":18,"updateTime":18,"relativeEntities":444,"label":445,"description":446,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":25},{},[448],{"id":29,"createTime":18,"updateTime":18,"relativeEntities":449,"slug":18,"properties":450,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":452,"statistic":18},[],{"title":451},{"EN":33},[],[454],{"id":37,"indexDatabase":455,"url":50,"indexYears":18,"academicFieldIds":460,"indexDatabaseRanking":18},{"id":39,"createTime":18,"updateTime":18,"relativeEntities":456,"label":457,"description":458,"key":46,"publicationTags":459,"standard":18},[],{"EN":42,"VI":42},{"EN":44,"VI":45},[48,49],[52],{"impactFactor":19,"impactFactorByYear":462,"i10Index":19,"i10IndexLast5Year":19,"totalPublication":55,"totalPublicationByYear":463,"totalCitation":57,"totalCitationByYear":464,"totalCitationPerPublication":57,"totalCitationPerPublicationByYear":465,"hindexLast5Year":55,"hindex":55},{"2023":55},{"2022":55},{"2022":57},{"2022":57},{"pages":467,"volume":469},{"VOID":468},"1-6",{"VOID":470},"6","2020-01-14",2020,"DONE_GET_PLATFORM_ID",[48],{"id":476,"createTime":477,"updateTime":478,"relativeEntities":479,"slug":480,"properties":481,"entityType":79,"verifyStatus":80,"verifyTime":492,"verifyNote":82,"languages":18,"translateLanguages":18,"viewCount":55,"primaryUrl":493,"fullTextUrl":18,"authors":494,"publicationType":243,"publisherRelationship":577,"citationCount":18,"citationInfo":18,"publishDate":612,"publishYear":613,"citationAnalyzeStatus":17,"lastCitationAnalyze":478,"indexDatabases":614,"openAccess":18,"references":18,"isForceReanalyzing":370},"e3084902-8907-4fca-8154-b3b715c8bf93","2024-02-14T16:38:22.485+00:00","2026-07-16T22:08:52.661+00:00",[],"SMARCB1-and-vimentin-positive-esophageal-carcinoma-with-undifferentiated-components-rhabdoid-features-and-a-good-prognosis-a-case-report",{"abstract":482,"title":484,"gsPaper":486,"references":488,"doi":490},{"EN":483},"Undifferentiated carcinoma of the esophagus with rhabdoid features is a very rare histologic finding that is occasionally associated with the loss of SWI\u002FSNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 (SMARCB1); however, until now, few survey reports of this type of tumor have been published. In this study, we describe a case of esophageal carcinoma with undifferentiated components and rhabdoid features that was exclusively positive for vimentin and SMARCB1 in a patient with prolonged survival. A 67-year-old man complained of a stomachache and loss of appetite persisting for 1 month. He was then admitted to the hospital. Diagnostic imaging studies revealed a transdiaphragmatic circular ulcerative tumor of the esophagogastric region. Biopsy specimens showed undifferentiated round cell carcinoma. The patient underwent lower esophageal resection and total gastrectomy with lymph node dissection. Microscopic analysis revealed that most of the primary tumor consisted of large undifferentiated round cells and scattered rhabdoid cells. The tumor invaded the muscular layer in the esophagus and the subserosal layer in the stomach, and metastasis was noted in only one lymph node. Immunohistochemical analysis revealed that the round and rhabdoid cells found in the primary tumor were diffusely positive for SMARCB1 and vimentin. The tumor displayed focal positivity for the anti-pan-cytokeratin antibody AE1\u002FAE3. In the positive lymph node, round undifferentiated carcinoma cells were admixed with squamous carcinoma cells that were positive for cytokeratin 5\u002F6 and 34βE12. The MIB-1 index was 19.7% and 0.5% for the round cells from the primary tumor and epithelial cells from the metastatic lymph node lesion, respectively, and 70.1% for the round cells from the metastatic lymph node lesion. The patient has been alive for 10 years after surgery without tumor recurrence. We reported a rare case of esophageal carcinoma with undifferentiated components, rhabdoid features, and a good prognosis.",{"EN":485},"SMARCB1- and vimentin-positive esophageal carcinoma with undifferentiated components, rhabdoid features, and a good prognosis: a case report",{"VOID":487},"[\"6842704227762410119\"]",{"VOID":489},"Shinghi AD, Seethala RR, Nason K, Foxwell TJ, Roche RL, McGrath KM, Levy RM, Luketich JD, Davison JM. Undifferentiated carcinoma of the esophagus: a clinicopathological study of 16 cases. Hum Pathol. 2015;46:366–75.\nMontgomery E, Field JK, Boffetta P, Daigo Y, Shimizu M, Shimoda T. In: Bosman FT, Carneiro F, Hruban RH, Theise ND, editors. World Health Organization classification of tumours of the digestive system. 4th ed, volume 3. Lyon: IARC Press; 2010. p. 18–24.\nRaza MA, Mazzara PF. Sarcomatoid carcinoma of esophagus. Arch Pathol Lab Med. 2011;135:945–8.\nMadan AK, Long AE, Weldon CB, Jaffe BM. Esophageal carcinosarcoma. J Gastrointest Surg. 2001;5:414–7.\nOoi A, Kawahara E, Okada Y, Mizukami Y, Sugawara S, Noto Y, Fujita H. Carcinosarcoma of the esophagus. An immunohistochemical and electron microscopic study. Acta Pathol Jpn. 1986;36:151–9.\nTakubo K, Nakamura K, Sawabe M, Arai T, Esaki Y, Miyashita M, Mafune K, Tanaka Y, Sasajima K. Primary undifferentiated small cell carcinoma of the esophagus. Hum Pathol. 1999;30:216–21.\nTerada T. Small cell neuroendocrine carcinoma of the esophagus: report of 6 cases with immunohistochemical and molecular genetic analysis of KIT and PDGFRA. Int J Clin Exp Pathol. 2013;6:485–91.\nShimizu K, Takiyama W, Mandai K, Tanada M, Kawabuchi Y, Heike Y. Undifferentiated carcinoma with lymphoid infiltration of the esophagus: a case report. Jan J Clin Oncol. 1999;29:494–7.\nYamada T, Tatsuzawa Y, Yagi S, Fujioka S, Kitagawa S, Nakagawa M, Minato H, Kurumaya H, Matsunou H. Lymphoepithelioma-like esophageal carcinoma: report of a case. Surg Today. 1999;29:542–4.\nTerada T. Epstein-Barr virus associated lymphoepithelial carcinoma of the esophagus. Int J Clin Exp Med. 2013;6:219–26.\nNg WC, Leong HT, Ma KF, Yip WL, Suen WM. Malignant rhabdoid tumour of the oesophagus: a case report. J Clin Pathol. 2003;56:713–4.\nVarghese LR, Stanley MW, Lucido ML, Mallery S, Lai R, Bardales RH. Esophageal carcinoma with a rhabdoid phenotype: a case report of diagnosis by endoscopic ultrasound-guided fine-needle aspiration. Diagn Cytopathol. 2005;33:407–11.\nAgaimy A, Rau TT, Hartmann A, Stoehr R. SMARCB1(INI1)-negative rhabdoid carcinomas of the gastrointestinal tract: clinicopathologic and molecular study of a highly aggressive variant with literature review. Am J Surg Pathol. 2014;38:910–20.\nAgaimy A, Daum O, Märkl B, Lichtmannegger I, Michal M, Hartmann A. SWI\u002FSNF complex-deficient undifferentiated\u002Frhabdoid carcinomas of the gastrointestinal tract: a series of 13 cases highlighting mutually exclusive loss of SMARCA4 and SMARCA2 and frequent co-inactivation of SMARCB1 and SMARCA2. Am J Surg Pathol. 2016;40:544–53.\nDadone B, Fontaine D, Mondot L, Cristofari G, Jouvet A, Godfraind C, Varlet P, Ranchère-Vince D, Coindre JM, Gastaud L, Baudoin C, Peyron AC, Thyss A, Coutts M, Michiels JF, Pedeutour F, Burel-Vandenbos F. Meningeal SWI\u002FSNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily B member 1 (SMARCB1)-deficient tumours: an emerging group of meningeal tumours. Neuropathol Appl Neurobiol. 2017;43:433–49.\nHollmann T, Hornick JL. INI-deficient tumors: diagnostic features and molecular genetics. Am J Surg Pathol. 2011;35:e47–63.\nWilson BG, Roberts CW. SWI\u002FSNF nucleosome remodellers and cancer. Nat Rev Cancer. 2011;11:481–92.\nUeyama T, Nagai E, Yao T, Tsuneyoshi M. Vimentin-positive gastric carcinomas with rhabdoid features. A clinicopathologic and immunohistochemical study. Am J Surg Pathol. 1993;17:813–9.\nMirza A, Foster L, Valentine H, Welch I, West CM, Pritchard S. Investigation of the epithelial to mesenchymal transition markers S100A4, vimentin and Snail1 in gastroesophageal junction tumors. Dis Esophagus. 2014;27:485–92.\nAgaimy A, Bertz S, Cheng L, Hes O, Junker K, Keck B, Lopez-Beltran A, Stöckle M, Wullich B, Hartmann A. Loss of expression of the SWI\u002FSNF complex is a frequent event in undifferentiated\u002Fdedifferentiated urothelial carcinoma of the urinary tract. Virchows Arch. 2016;469:321–30.\nSchartinger VH, Falkeis C, Laimer K, Sprinzl GM, Riechelmann H, Rasse M, Virgolini I, Dudás J. Neuroendocrine differentiation in head and neck squamous cell carcinoma. J Laryngol Otol. 2012;126:1261–70.\nSidney LE, Branch MJ, Dunphy SE, Dua HS, Hopkinson A. Concise review: evidence for CD34 as a common marker for diverse progenitors. Stem Cells. 2014;32:1380–9.\nKishida H, Sodemoto Y, Ushigome S, Kubota S, Kataba Y. Non-oat cell small cell carcinoma of the esophagus. Report of a case with ultrastructural observation. Acta Pathol Jpn. 1983;33:403–13.\nGoldblum JR, Lamps LW, McKenney JK, Myers JL. Rosai and Ackerman’s surgical pathology. Philadelphia: ELSEVIER; 2018. p. 511–9.\nKhokhar N, Nasir H, Amir M, Hassan S, Khan K, Ahmed M. Lymphoepithelioma-like carcinoma of the esophagus: a rare tumor. J Coll Physicians Surg Pak. 2017;27:S114–6.\nNakasono M, Hirokawa M, Suzuki M, Takizawa H, Okitsu H, Okamura S, Muguruma N, Ito S, Sano T. Lymphoepithelioma-like carcinoma of the esophagus: report of a case with non-progressive behavior. J Gastroenterol Hepatol. 2007;22:2344–7.\nSashiyama H, Nozawa A, Kimura M, Momura E, Tamaru JI, Ninomiya E, Koide Y, Iino M, Ozawa K. Case report: a case of lymphoepithelioma-like carcinoma of the oesophagus and review of the literature. J Gastroenterol Hepatol. 1999;14:534–9.\nChino O, Kijima H, Shimada H, Mizutani K, Nishi T, Tanaka H, Tanaka M, Serizawa A, Tajima T, Makuuchi H. Esophageal squamous cell carcinoma with lymphoid stroma: report of 3 cases with immunohistochemical analysis. Gatrointest Endosc. 2001;54:513–7.\nTakubo K, Lambie NK. Barrett’s adenocarinoma of the esophagus with lymphoid stroma. J Clin Gastroenterol. 2001;33:141–4.\nWang HH, Wu MS, Shun CT, Wang HP, Lin CC, Lin JT. Lymphoepithelioma-like carcinoma of the stomach: a subset of gastric carcinoma with distinct clinicopathological features and high prevalence of Epstein-Barr virus infection. Hepatogastroenterol. 1999;46:1214–9.\nTsang WYW, Chan JKC. Lymphoepithelial carcinoma. In: Barnes L, Eveson JW, Reichart P, Sidransky, editors. . Lyon: IARC Press; 2005. p. 18–9.",{"VOID":491},"10.1186\u002Fs40792-019-0562-4","2024-06-25T05:45:27.320+00:00","https:\u002F\u002Fsurgicalcasereports.springeropen.com\u002Farticles\u002F10.1186\u002Fs40792-019-0562-4",[495,519,532,547,562],{"id":496,"sortIndex":19,"researcher":18,"roles":497,"affiliations":498,"properties":516,"displayName":518,"givenName":18,"familyName":18},"bfe07f2f-9995-42c6-af86-9b98695779a6",[88],[499,507],{"id":500,"sortIndex":19,"affiliation":501,"properties":18},"e58b5d9f-afae-447d-be64-f40ed86af73d",{"id":500,"createTime":18,"updateTime":18,"relativeEntities":502,"slug":18,"properties":503,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":506,"statistic":18},[],{"title":504},{"VI":505},"Department of Surgery, Fukui General Hospital, Fukui, Japan",[],{"id":508,"sortIndex":55,"affiliation":509,"properties":515},"347f3503-7043-43b5-b8c2-ab6066bc489f",{"id":508,"createTime":18,"updateTime":18,"relativeEntities":510,"slug":18,"properties":511,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":514,"statistic":18},[],{"title":512},{"VI":513},"Department of Surgery, Japan Community Health Care Organization Fukui Katsuyama General Hospital, Fukui, Japan",[],{},{"title":517},{"VI":518},"Hideki Nagano",{"id":520,"sortIndex":55,"researcher":18,"roles":521,"affiliations":522,"properties":529,"displayName":531,"givenName":18,"familyName":18},"48b17192-9b95-4b0a-992b-f5921cc0438c",[88],[523],{"id":500,"sortIndex":19,"affiliation":524,"properties":18},{"id":500,"createTime":18,"updateTime":18,"relativeEntities":525,"slug":18,"properties":526,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":528,"statistic":18},[],{"title":527},{"VI":505},[],{"title":530},{"VI":531},"Toshimasa Izumi",{"id":533,"sortIndex":57,"researcher":18,"roles":534,"affiliations":535,"properties":544,"displayName":546,"givenName":18,"familyName":18},"2b6ae2f1-0e97-4d4b-9212-1f54676ad7d4",[88],[536],{"id":537,"sortIndex":19,"affiliation":538,"properties":18},"3c7a3cf1-247f-488b-9e60-b00af49b4e6b",{"id":537,"createTime":18,"updateTime":18,"relativeEntities":539,"slug":18,"properties":540,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":543,"statistic":18},[],{"title":541},{"VI":542},"Department of Pathology, Fukui General Hospital, Fukui, Japan",[],{"title":545},{"VI":546},"Ei Kawahara",{"id":548,"sortIndex":131,"researcher":18,"roles":549,"affiliations":550,"properties":559,"displayName":561,"givenName":18,"familyName":18},"10841d9e-8963-4b9a-bba8-4e0c9f826c0a",[88],[551],{"id":552,"sortIndex":19,"affiliation":553,"properties":18},"d2b5927e-822e-4eb7-a30c-333859435654",{"id":552,"createTime":18,"updateTime":18,"relativeEntities":554,"slug":18,"properties":555,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":558,"statistic":18},[],{"title":556},{"VI":557},"Department of Pathology, Kanazawa University, Kanazawa, Japan",[],{"title":560},{"VI":561},"Takeru Oyama",{"id":563,"sortIndex":145,"researcher":18,"roles":564,"affiliations":565,"properties":574,"displayName":576,"givenName":18,"familyName":18},"762e2fa9-bb65-4b51-9c06-8710d4e80df0",[88],[566],{"id":567,"sortIndex":19,"affiliation":568,"properties":18},"db3af7af-4654-43fd-8a58-e286e852de16",{"id":567,"createTime":18,"updateTime":18,"relativeEntities":569,"slug":18,"properties":570,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":573,"statistic":18},[],{"title":571},{"VI":572},"1st Department of Surgery, Faculty of Medicine, University of Fukui, Eiheiji-cho, Japan",[],{"title":575},{"VI":576},"Takanori Goi",{"url":493,"publisher":578,"properties":607},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":579,"slug":10,"properties":580,"entityType":16,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":19,"subjectFields":583,"manageAffiliations":588,"indexDatabases":594,"url":18,"thumbnailPath":18,"statistic":602,"gsStatistic":18,"type":18,"analyzePriority":18},[],{"title":581,"eissn":582},{"EN":13},{"VOID":15},[584],{"id":22,"createTime":18,"updateTime":18,"relativeEntities":585,"label":586,"description":587,"parentId":18,"standard":18,"scholarHubFieldId":18},[],{"EN":25},{},[589],{"id":29,"createTime":18,"updateTime":18,"relativeEntities":590,"slug":18,"properties":591,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":593,"statistic":18},[],{"title":592},{"EN":33},[],[595],{"id":37,"indexDatabase":596,"url":50,"indexYears":18,"academicFieldIds":601,"indexDatabaseRanking":18},{"id":39,"createTime":18,"updateTime":18,"relativeEntities":597,"label":598,"description":599,"key":46,"publicationTags":600,"standard":18},[],{"EN":42,"VI":42},{"EN":44,"VI":45},[48,49],[52],{"impactFactor":19,"impactFactorByYear":603,"i10Index":19,"i10IndexLast5Year":19,"totalPublication":55,"totalPublicationByYear":604,"totalCitation":57,"totalCitationByYear":605,"totalCitationPerPublication":57,"totalCitationPerPublicationByYear":606,"hindexLast5Year":55,"hindex":55},{"2023":55},{"2022":55},{"2022":57},{"2022":57},{"pages":608,"volume":610},{"VOID":609},"1-8",{"VOID":611},"5","2019-01-16",2019,[48],{"id":616,"createTime":617,"updateTime":618,"relativeEntities":619,"slug":620,"properties":621,"entityType":79,"verifyStatus":80,"verifyTime":630,"verifyNote":82,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":631,"fullTextUrl":18,"authors":632,"publicationType":243,"publisherRelationship":720,"citationCount":19,"citationInfo":754,"publishDate":757,"publishYear":755,"citationAnalyzeStatus":17,"lastCitationAnalyze":758,"indexDatabases":759,"openAccess":18,"references":760,"isForceReanalyzing":370},"a8628b43-50ff-45b1-8021-ef5c062f6d0c","2024-01-12T23:32:49.572+00:00","2026-07-13T20:30:09.928+00:00",[],"A-case-of-successful-slide-tracheoplasty-for-long-segment-congenital-tracheal-stenosis-in-a-neonate-with-a-congenital-diaphragmatic-hernia-and-Fallot-s-tetralogy",{"abstract":622,"title":624,"gsPaper":626,"doi":628},{"EN":623},"Congenital tracheal stenosis (CTS) is a rare and life-threatening airway disorder, which is often associated with cardiac malformations. Among them, neonatal symptomatic CTS with cardiac malformations has an extremely poor prognosis. In contrast to cardiac malformation, congenital diaphragmatic hernia (CDH) has rarely been associated with CTS. We report a neonatal case in which slide tracheoplasty and intracardiac repair were performed simultaneously for CTS and Fallot’s tetralogy (TOF). An infant with left CDH and Fallot's tetralogy (TOF) was born by cesarean section at 38 weeks of gestation. At the time of resuscitation, a 2.5 mm (ID) endotracheal tube could only be inserted just below the vocal cords. After repairing the CDH at 3 days of age, planned extubation was performed at 7 days of age. However, the patient required re-intubation due to life-threatening episodes after 2 days of the extubation. Enhanced CT revealed a long segment CTS from the upper trachea to the right bronchus (length of stenosis: 40 mm, minimum inner diameter: 2 mm). At 24 days of age, veno-arterial extracorporeal membrane oxygenation (ECMO) was introduced due to severe respiratory failure. At 28 days of age, slide tracheoplasty and palliative right ventricular outflow tract reconstruction (RVOTR) was performed with cardiopulmonary bypass (CPB). After tracheoplasty, a 3.5 mm tracheal (ID) tube could be placed in the reconstructed trachea in a patient with CTS. ECMO was completed 7 days after the operation. On the 17th day after the operation, he was extubated successfully. He was discharged 5 months after birth with home oxygenation therapy. We reported the successful simultaneous correction of slide tracheoplasty and palliative RVOTR for a neonate with CDH. ECMO was used for respiratory management before and after surgery.",{"EN":625},"A case of successful slide tracheoplasty for long-segment congenital tracheal stenosis in a neonate with a congenital diaphragmatic hernia and Fallot’s 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Prognostic factors in the surgical treatment of congenital tracheal stenosis: a multicenter analysis of the literature. J Pediatr Surg. 2006;41(1):221–5.",{},{"id":299,"text":765,"url":301,"identifiers":766},"Arcieri L, Moschetti R, Assanta N, Cantinotti M, Baggi R, Mirabile L, Murzi B. Successful simultaneous correction of complex congenital tracheal stenosis and tetralogy of fallot. World J Pediatr Congenit Heart Surg. 2012;3(4):511–4.",{"doi":303},{"id":768,"text":769,"url":770,"identifiers":771},"76a05eaf-c4a0-41ba-8241-8ac57cd92215","Herrera P, Caldarone C, Forte V, Campisi P, Holtby H, Chait P, Chiu P, Cox P, Yoo SJ, Manson D, Kim PC. The current state of congenital tracheal stenosis. Pediatr Surg Int. 2007;23(11):1033–44.","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs00383-007-1945-3",{"doi":772},"10.1007\u002Fs00383-007-1945-3",{"id":299,"text":774,"url":301,"identifiers":775},"Eliliot M, Roebuck D, Noctor C, et al. The management of congenital tracheal stenosis. Int J Pediatr Otorhinolaryngol. 2003;67(Suppl 1):S183–92.",{"doi":303},{"id":299,"text":777,"url":301,"identifiers":778},"Wang S, Zhang H, Zhu L, Zhen J, Liu J, Xu Z. Surgical management of congenital tracheal stenosis associated with tracheal bronchus and congenital heart disease. Eur J Cardiothorac Surg. 2016;49:1201–6.",{"doi":303},{"id":780,"text":781,"url":782,"identifiers":783},"20601d0e-ed09-443a-80a3-7ebbcf4fe81a","Okamoto T, Nishijima E, Maruo A, Yokoi A, Takamizawa S, Satoh S, et al. Congenital tracheal stenosis: the prognostic significance of associated cardiovascular anomalies and the optimal timing of surgical treatment. J Pediatr Surg. 2009;44:325–8.","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0022346808009445",{"doi":784},"10.1016\u002Fj.jpedsurg.2008.10.080",{"id":786,"text":787,"url":788,"identifiers":789},"64b7d8a4-9ca0-41f4-8ae1-3f7cdf8586e6","Tsugawa C, Nishijima E, Muraji T, Satoh S, Takamizawa S, Yamaguchi M, Yoshimura N, Oka S, Kimura K. Tracheoplasty for long segment congenital tracheal stenosis: analysis of 29 patients over two decades. J Pediatr Surg. 2003;38(12):1703–6.","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0022346803006353",{"doi":790},"10.1016\u002Fj.jpedsurg.2003.08.037",{"id":792,"text":793,"url":794,"identifiers":795},"3765ba8c-bacf-4706-b9c8-45707d60745d","Morita K, Yokoi A, Fukuzawa H, Hisamatsu C, Endo K, Okata Y, Tamaki A, Mishima Y, Oshima Y, Maeda K. Surgical intervention strategies for congenital tracheal stenosis associated with a tracheal bronchus based on the location of stenosis. Pediatr Surg Int. 2016;32(9):915–9.","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs00383-016-3928-8",{"doi":796},"10.1007\u002Fs00383-016-3928-8",{"id":798,"text":799,"url":800,"identifiers":801},"237ca604-169e-4e68-955b-889e602cacd1","Yokoi A, Oshima Y, Nishijima E. The role of adjunctive procedures in reducing postoperative tracheobronchial obstruction in single lung patients with congenital tracheal stenosis undergoing slide tracheoplasty. J Pediatr Surg. 2017;52(5):677–9.","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0022346817300465",{"doi":802},"10.1016\u002Fj.jpedsurg.2017.01.014",{"id":299,"text":804,"url":301,"identifiers":805},"Chung SR, Yang JH, Jun TG, Kim WS, Kim YH, Kang IS, Huh J, Song JY, Cho J. Clinical outcomes of slide tracheoplasty in congenital tracheal stenosis. Eur J Cardiothorac Surg. 2015;47(3):537–42.",{"doi":303},{"id":299,"text":807,"url":301,"identifiers":808},"DeMarcantonio MA, Hart CK, Yang CJ, Tabangin M, Rutter MJ, Bryant R, Manning PB, de Alarcón A. Slide tracheoplasty outcomes in children with congenital pulmonary malformations. Laryngoscope. 2017;127(6):1283–7.",{"doi":303},{"id":299,"text":810,"url":301,"identifiers":811},"Chou AK, Huang SC, Chen SJ, Huang PM, Wang JK, Wu MH, Chen YS, Chang CI, Chiu IS, Wu ET. Unilateral lung agenesis–detrimental roles of surrounding vessels. Pediatr Pulmonol. 2007;42(3):242–8.",{"doi":303},{"id":299,"text":813,"url":301,"identifiers":814},"Backer CL, Kelle AM, Mavroudis C, Rigsby CK, Kaushal S, Holinger LD. Tracheal reconstruction in children with unilateral lung agenesis or severe hypoplasia. Ann Thorac Surg. 2009;88(2):624–30.",{"doi":303},{"id":299,"text":816,"url":301,"identifiers":817},"Nose K, Kamata S, Sawai T, Tazuke Y, Usui N, Kawahara H, Okada A. Airway anomalies in patients with congenital diaphragmatic hernia. 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A 55-year-old man with acute lower-limb ischemia was referred to our hospital after endovascular intervention failed and underwent above-the-knee amputation for severe limb necrosis. On postoperative day 8, he developed small bowel necrosis and underwent resection. Histopathological examination of the resected bowel revealed that the submucosal arterial emboli were positive for the markers of squamous cells. He had unresectable lung squamous cell carcinoma with left atrium invasion. The subsequent embolisms were thought to be caused by the advanced lung cancer. ATE is rare but should be considered as a differential diagnosis for unidentified arterial occlusion.",{"EN":828},"Acute lower limb ischemia and intestinal necrosis due to arterial tumor embolism from advanced lung cancer: a case report and literature review",{"VOID":830},"[\"13087759337863029291\"]",{"VOID":832},"Miroslav M, Lazar D, Aleksandar M, Predrag D, Svetozar P. Rare forms of peripheral arterial embolism. Vascular. 2005;13:222–9.\nXiromeritis N, Klonaris C, Papas S, Valsamis M, Bastounis E. Recurrent peripheral arterial embolism from pulmonary cancer. Int Angiol. 2000;19:79–83.\nHeitmiller RF. Prognostic significance of massive bronchogenic tumor embolus. Ann Thorac Surg. 1992;53:153–5.\nChandler C. Malignant arterial tumor embolization. J Surg Oncol. 1993;52:197–202.\nDahle E, Gogenur I, Norgaard P. Intestinal necrosis in young patient due to arterial tumour embolism. BMJ Case Rep 2012 Sep 14;2012. pii: bcr0120125558. doi: https:\u002F\u002Fdoi.org\u002F10.1136\u002Fbcr.01.2012.5558.\nPrioleau PG, Katzenstein AA. Major peripheral arterial occlusion due to malignant tumor embolism. Cancer. 1987;42:2009–14.\nTopalian SL, Sznol M, McDermott DF, Kluger HM, Carvajal RD, Sharfman WH, et al. Survival, durable response, and long-term safety in patients with previously treated advanced renal cell carcinoma receiving nivolumab. J Clin Oncol. 2015;33:2013–20.\nTaber RE. Massive systemic tumor embolization during pneumonictomy. Ann Surg. 1061;154:263–8.\nWebb DF, Tomatis L, Taber RE, Ponka JL. Successful surgical management of superior mesenteric and femoral artery tumor emboli resulting from pneumonectomy. Henry Ford Hosp Bull. 1965;13:299–302.\nWhyte RI, Starkey TD, Orringer MB, Mich AA. Tumor emboli from lung neoplasms involving the pulmonary vein. 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and the resultant peptic ulcer related to an enteric duplication has been quite rarely reported in the literature. We herein report the case of a 4-year-old girl who presented with hypergastrinemia and a duodenal ulcer at 2 years of age. She had been followed up with a proton pump inhibitor, which resulted in resolution of the ulcer; however, unexplained hypergastrinemia had continued. A cystic lesion at the antrum was discovered at 4 years of age, which we suspected to be a gastric duplication. After we resected the lesion, the hypergastrinemia resolved without recurrence of the duodenal ulcer. The histology was compatible with a gastric duplication, and the lumen was lined with antral mucosa that strongly stained positive for gastrin. We presumed that the antral mucosa inside the duplication in our case had no hydrogen ion feedback inhibition of gastrin release from gastrin cells and increased release of gastrin from the mucosa inside the duplication led to the duodenal ulcer. Only two cases have been reported in the literature that had hypergastrinemia related to enteric duplication. Gastric duplication should be included in the differential diagnosis of sustained hypergastrinemia in children.",{"EN":1023},"Hypergastrinemia and a duodenal ulcer caused by gastric duplication",{"VOID":1025},"[\"9808083199916701170\"]",{"VOID":1027},"Murty T, Bhargava R, Rakas F. Gastroduodenal duplication. J Pediatr Surg. 1992;4:515–7.\nSiddiqui A, Shamberger R, Filler R, Perez-Atayde A, Lillehei C. Enteric duplications of the pancreatic head: definitive management by local resection. J Pediatr Surg. 1998;33:1117–21.\nStephen T, Bendon R, Nagaraj H, Sachdeva R. Antral duplication cyst: a cause of hypergastrinemia, recurrent peptic ulceration, and hemorrhage. J Pediatr Gastroenterol Nutr. 1998;26:216–8.\nHolcomb G, Gheissari A, O’Neill J, Shorter N, Bishop H. Surgical management of alimentary tract duplications. Ann Surg. 1989;209:167–74.\nCunningham S, Hansel D, Fishman E, Cameron J. Foregut duplication cyst of the stomach. J Gastrointest Surg. 2006;10:620–1.\nArnold R. Diagnosis and differential diagnosis of hypergastrinemia. Wien Klin Wochenschr. 2007;119:564–9.\nPashankar D, Israle D, Jevon G, Buchan A. Effect of long term treatment on antral G and D cells in children. 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               \u003Cjats:title>Background\u003C\u002Fjats:title>\n                \u003Cjats:p>The rate of residual liver recurrence after the resection of colorectal liver metastases is high, and most cases recur within 5 years of the initial hepatectomy. Here, we report two cases of residual liver recurrence after radical resection of colorectal liver metastases after a long recurrence-free survival period.\u003C\u002Fjats:p>\n              \u003C\u002Fjats:sec>\u003Cjats:sec>\n                \u003Cjats:title>Case presentation\u003C\u002Fjats:title>\n                \u003Cjats:p>Case 1 involved a 62-year-old woman treated for ascending colon cancer in April 2011 who underwent right hepatectomy for synchronous colorectal liver metastasis in April 2012. However, in September 2021, computed tomography revealed residual recurrence in the lateral segment of the liver, and a lateral segmentectomy of the liver was performed. In Case 2, a 52-year-old man treated for cecal cancer in July 2002 underwent lateral segmentectomy of the liver for metachronous colorectal liver metastasis in October 2006. Subsequently, there was no recurrence; however, computed tomography showed residual liver recurrence in the right lobe of the liver in October 2021, and an expanded posterior hepatic segmentectomy was performed.\u003C\u002Fjats:p>\n                \u003Cjats:p>Histopathological findings in both cases were consistent with colorectal liver metastases.\u003C\u002Fjats:p>\n              \u003C\u002Fjats:sec>\u003Cjats:sec>\n                \u003Cjats:title>Conclusions\u003C\u002Fjats:title>\n                \u003Cjats:p>We encountered two cases in which residual liver recurrence was observed after a long period of recurrence-free survival. Although rare, there have been a few cases of late recurrence of liver metastases after radical resection of cancer liver metastases.\u003C\u002Fjats:p>\n              \u003C\u002Fjats:sec>",{"EN":1233},"Two cases of colorectal liver metastasis with residual liver recurrence after a long recurrence-free survival 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Current management of colorectal liver metastases. Surg Oncol Clin N Am. 2000; 9: 853–76",{"doi":1497},"10.1016\u002FS1055-3207(18)30126-1",{"id":18,"text":1499,"url":18,"identifiers":1500},"Hasegawa K, Saiura A, Takayama T, Miyagawa S, Yamamoto J, Ijichi M, et al. Adjuvant oral uracil-tegafur with leucovorin for colorectal cancer liver metastases: a randomized controlled trial. PLoS ONE. 2016;11: e0162400.",{"doi":1501},"10.1371\u002Fjournal.pone.0162400",{"id":18,"text":1503,"url":18,"identifiers":1504},"de Jong MC, Mayo SC, Pulitano C, Lanella S, Ribero D, Strub J, et al. Repeat curative intent liver surgery is safe and effective for recurrent colorectal liver metastasis: results from an international multi-institutional analysis. J Gastrointest Surg. 2009;13:2141–51.",{"doi":1505},"10.1007\u002Fs11605-009-1050-0",{"id":18,"text":1507,"url":18,"identifiers":1508},"Meyerhardt JA, Mangu PB, Flynn PJ, Korde L, Loprinzi CL, Minsky BD, et al. Follow-up care, surveillance protocol, and secondary prevention measures for survivors of colorectal cancer: American society of clinical oncology clinical practice guideline endorsement. J Clin Oncol. 2013;31:4465–70.",{"doi":1509},"10.1200\u002FJCO.2013.50.7442",{"id":18,"text":1511,"url":18,"identifiers":1512},"Hardiman KM, Felder SI, Friedman G, Migaly J, Paquette IM, Feingold DL. The American society of colon and rectal surgeons clinical practice guidelines for the surveillance and survivorship care of patients after curative treatment of colon and rectal cancer. Dis Colon Rectum. 2021;64:517–33.",{"doi":1513},"10.1097\u002FDCR.0000000000001984",{"id":18,"text":1515,"url":18,"identifiers":1516},"Seo SI, Lim SB, Yoon YS, Kim CW, Yu CS, Kim TW, et al. Comparison of recurrence patterns between ≤5 years and >5 years after curative operations in colorectal cancer patients. J Surg Oncol. 2013;108:9–13.",{"doi":1517},"10.1002\u002Fjso.23349",{"id":18,"text":1519,"url":18,"identifiers":1520},"Daniels AM, Vogelaar JFJ. Late onset pulmonary metastasis more than 10 years after primary sigmoid carcinoma. World J Gastrointest Pathophysiol. 2017;8:96–9.",{"doi":1521},"10.4291\u002Fwjgp.v8.i2.96",{"id":18,"text":1523,"url":18,"identifiers":1524},"Ikuta K, Hirakawa H, Ikeuchi M, Shio S. Lung metastasis occurring 12 years after colonic cancer surgery. Intern Med. 2022;61:1619–20.",{"doi":1525},"10.2169\u002Finternalmedicine.8054-21",{"id":18,"text":1527,"url":18,"identifiers":1528},"Yonenaga Y, Yokoyama S. Isolated liver metastasis detected 11 years after the curative resection of rectal cancer: a case report. World J Clin Cases. 2021;9:8923–31.",{"doi":1529},"10.12998\u002Fwjcc.v9.i29.8923",{"id":18,"text":1531,"url":18,"identifiers":1532},"Nagano T, Itoh S, Miyashita Y, Shimagaki T, Wang H, Kurihara T, et al. Late recurrence of cancer stem cell-positive colorectal cancer liver metastases after 15 years. Clin J Gastroenterol. 2021;14:613–6.",{"doi":1533},"10.1007\u002Fs12328-020-01330-1",{"id":18,"text":1535,"url":18,"identifiers":1536},"Battula N, Tsapralis D, Mayer D, Isaac J, Muiesan P, Sutcliffe RP, et al. Repeat liver resection for recurrent colorectal metastases: a single-centre, 13-year experience. HPB (Oxford). 2014;16:157–63.",{"doi":1537},"10.1111\u002Fhpb.12096",{"id":18,"text":1539,"url":18,"identifiers":1540},"Metcalfe MS, Mullin EJ, Maddern GJ. Choice of surveillance after hepatectomy for colorectal metastases. Arch Surg. 2004;139:749–54.",{"doi":1541},"10.1001\u002Farchsurg.139.7.749",{"id":18,"text":1543,"url":18,"identifiers":1544},"Okamura R, Hida K, Nishizaki D, Sugihara K, Sakai Y. Proposal of a stage-specific surveillance strategy for colorectal cancer patients: a retrospective analysis of Japanese large cohort. Eur J Surg Oncol. 2018;44:449–55.",{"doi":1545},"10.1016\u002Fj.ejso.2018.01.080",{"id":18,"text":1547,"url":18,"identifiers":1548},"Cho YB, Chun HK, Yun HR, Lee WS, Yun SH, Lee WY. Clinical and pathologic evaluation of patients with recurrence of colorectal cancer five or more years after curative resection. Dis Colon Rectum. 2007;50:1204–10.",{"doi":1549},"10.1007\u002Fs10350-007-0247-0",{"id":18,"text":1551,"url":18,"identifiers":1552},"Wurster EF, Tenckhoff S, Probst P, Jensen K, Dölger E, Knebel P, et al. A systematic review and meta-analysis of the utility of repeated versus single hepatic resection for colorectal cancer liver metastases. HPB. 2017;19:491–7.",{"doi":1553},"10.1016\u002Fj.hpb.2017.02.440",{"id":1555,"createTime":1556,"updateTime":1557,"relativeEntities":1558,"slug":1559,"properties":1560,"entityType":79,"verifyStatus":80,"verifyTime":1571,"verifyNote":82,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":1572,"fullTextUrl":18,"authors":1573,"publicationType":243,"publisherRelationship":1734,"citationCount":18,"citationInfo":18,"publishDate":1768,"publishYear":1769,"citationAnalyzeStatus":1770,"lastCitationAnalyze":1771,"indexDatabases":1772,"openAccess":18,"references":18,"isForceReanalyzing":370},"9cfd6c67-d1bc-4e9f-8142-ccc59b3ccb07","2024-01-09T00:09:17.520+00:00","2026-07-08T05:50:05.609+00:00",[],"Management-of-horizontal-duodenal-perforation-a-report-of-three-cases-and-review-of-literature",{"abstract":1561,"title":1563,"gsPaper":1565,"references":1567,"doi":1569},{"EN":1562},"Perforation of the horizontal duodenum is very rare due to the presence in retroperitoneal space. It depicts an unusual clinical picture and is difficult to diagnose, leading to increased morbidity and mortality. The treatment strategies are usually varied and based on small series of cases, literature reviews, and expert opinions. Here, we presented three cases of horizontal duodenal perforation in three different clinical processes. The first case, a 30-year-old male patient, presented with abdominal pain and hematemesis after experiencing a physical assault on the previous day. Computed tomography (CT) scan showed rupture of the horizontal duodenum. It was repaired by side-to-side duodenojejunostomy. Postoperatively, he had anastomotic leakage, disseminated intravascular coagulation, and pulmonary failure and recovered after a long hospital stay. The second case, an 81-year-old female, had duodenal perforation with endoscopic coagulation of the bleeding diverticulum. Segmental resection of the duodenum and side-to-side duodenojejunostomy were performed. Postoperatively, there was slight anastomotic leakage, but surgical intervention was not needed. The third case, an 89-year-old female, was a patient with obstructive jaundice due to pancreas head carcinoma, who developed perforation of the horizontal duodenum during endoscopic retrograde cholangiopancreatography (ERCP). After unsuccessful conservative management, duodenojejunostomy at the perforated site and gastric bypass were performed. The postoperative course was uneventful. Early suspicion and investigation is necessary for cases of abdominal injuries. CT scan is the investigation of choice. The management options should be based on the clinical condition of the patient, comorbidities, surgical expertise, existing guidelines, and available resources.",{"EN":1564},"Management of horizontal duodenal perforation: a report of three cases and review of literature",{"VOID":1566},"[]",{"VOID":1568},"Jansen M, Du Toit DF, Warren BL. Duodenal injuries: surgical management adapted to circumstances. Injury. 2002;33(7):611–5.\nPhilip NP, Singla S, Chakravarthi R, Philip NP. MDCT findings in iatrogenic duodenal perforation. J Evol Med Dent Sci. 2013;2(14):2397–401.\nCrippa S, Falconi M, Bettini R, Barugola G, Germenia S, Alvia R, Pederzoli P. Isolated blunt duodenal trauma: delayed diagnosis and favorable outcome with “quadruple tube” decompression. J Pancreas (Online). 2007;8(5):617–20.\nAssalia A, Suissa A, Ilivitzki A, Mahajna A, Yassin K, Hashmonai M, Krausz MM. Validity of clinical criteria in the management of endoscopic retrograde cholangiopancreatography-related duodenal perforations. Arch Surg. 2007;142(11):1059–64.\nTurner RC, Steffen CM, Boyd P. Endoscopic duodenal perforation: surgical strategies in a regional centre. World J Emerg Surg. 2014;9(1):11.\nGarcı’a Santos E, Soto Sa’nchez A, Verde JM, Marini CP, Asensio JA, Petrone P. Lesiones duodenales secundarias a traumatismo: revisión de la literatura. Cir Esp. 2015;93:68–74.\nMotomura Y, Akahoshi K, Gibo J, Kanayama K, Fukuda S, Hamada S, Otsuka Y, Kubokawa M, Kajiyama K, Nakamura K. Immediate detection of endoscopic retrograde cholangiopancreatography-related periampullary perforation: fluoroscopy or endoscopy? World J Gastroenterol. 2014;20(42):15797.\nBalasubramanian G, Vijayakumar C, Anbarasu I, Sudharsanan S, Raj Kumar N, Baskaran D. Isolated rupture of duodenum following blunt trauma abdomen: report of a case of avulsion of pylorus. Int Surg J. 2017;4(8)2845–7. doi:10.18203\u002F2349-2902.isj20173143.\nMoore EE, Cogbill TH, Malangoni MA, Jurkovich GJ, Champion HR, Gennarelli TA, McAninch JW, Pachter HL, Shackford SR, Trafton PG. Organ injury scaling, II: pancreas, duodenum, small bowel, colon, and rectum. J Trauma. 1990;30(11):1427–9.\nKim BS, Kim IG, Ryu BY, Kim JH, Yoo KS, Baik GH, Kim JB, Jeon JY. Management of endoscopic retrograde cholangiopancreatography-related perforations. J Korean Surg Soc. 2011;81(3):195–204.\nIvatury RR, Nallathambi MA, Gaudino J, Rohman M, Stahl WM. Penetrating duodenal injuries. Analysis of 100 consecutive cases. Ann Surg. 1985;202(2):153–8.\nChaudhry R, Tiwari GL, Singh Y. Damage control surgery for abdominal trauma. Medical Journal Armed Forces India. 2006;62(3):259–62.\nLiu Y, Wang D, Li Z. Endoscopic closure for EUS and ERCP related duodenal perforation by endoclips. Gastroenterol Res Pract. 2016;15:2016.\nClavien PA, Barkun J, de Oliveira ML, Vauthey JN, Dindo D, Schulick RD, de Santibañes E, Pekolj J, Slankamenac K, Bassi C, Graf R. The Clavien-Dindo classification of surgical complications: five-year experience. 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fibrous tumor (SFT) is a relatively rare mesenchymal tumor that mainly affects adults. Its prognosis is good after curative resection, but distant recurrences after 10 years or longer have been reported. Recurrent SFT usually arises as a local lesion; distant metastasis is rarely reported. Here, we report lung metastases that recurred a decade after excising a retroperitoneal primary SFT. A 44-year-old woman had an SFT resected from her right retroperitoneum at our hospital. Ten years later, at age 54, she underwent a lung resection after CT showed three suspected metastases in her left lung. All three were histologically diagnosed as lung metastases from the retroperitoneal SFT. However, whereas the primary SFT had 1–2 mitotic cells\u002F10 high power fields (HPF), the metastatic lesion increased malignancy, at 50\u002F10 HPF. Patients who have had resected SFTs should be carefully followed up, as malignancy may change in distant metastasis, as in this case.",{"EN":1783},"Retroperitoneal fibrous tumor recurring as lung metastases after 10 years: a case report",{"VOID":1566},{"EN":1786},"",{"VOID":1788},"Gold JS, Antonescu CR, Hajdu C, Ferrone CR, Hussain M, Lewis JJ, et al. Clinicopathologic correlates of solitary fibrous tumors. Cancer. 2002;94(4):1057–68.\nBaldi GG, Stacchiotti S, Mauro V, Dei Tos AP, Gronchi A, Pastorino U, et al. Solitary fibrous tumor of all sites: outcome of late recurrences in 14 patients. Clin Sarcoma Res. 2013;3:4.\nKlemperer P, Coleman BR. Primary neoplasms of the pleura. A report of five cases. Am J Ind Med. 1992;22(1):1–31.\nSaid JW, Nash G, Banks-Schlegel S, Sassoon AF, Shintaku IP. Localized fibrous mesothelioma: an immunohistochemical and electron microscopic study. Hum Pathol. 1984;15(5):440–3.\nEngland DM, Hochholzer L, McCarthy MJ. Localized benign and malignant fibrous tumors of the pleura. A clinicopathologic review of 223 cases. Am J Surg Pathol. 1989;13(8):640–58.\nMaki T, Fujino S, Misu K, Kaneko H, Inomata H, Omi M, et al. Integrally calcified solitary fibrous tumor in the retroperitoneum: a case report and review of the literature. Surg Case Rep. 2016;2(1):14.\nKunieda K, Tanaka Y, Nagao N, Yamaguchi K, Sano J, Osada S, et al. Large solitary fibrous tumor of the retroperitoneum: report of a case. Surg Today. 2004;34(1):90–3.\nKanthan R, Torkian B. Recurrent solitary fibrous tumor of the pleura with malignant transformation. Arch Pathol Lab Med. 2004;128(4):460–2.\nKrishnadas R, Froeschle PO, Berrisford RG. Recurrence and malignant transformation in solitary fibrous tumour of the pleura. Thorac Cardiovasc Surg. 2006;54(1):65–7.",{"VOID":1790},"10.1186\u002Fs40792-021-01209-4","2024-06-24T12:55:18.954+00:00","https:\u002F\u002Fsurgicalcasereports.springeropen.com\u002Farticles\u002F10.1186\u002Fs40792-021-01209-4",[1794,1809,1822,1835,1848,1861,1874,1887,1900],{"id":1795,"sortIndex":19,"researcher":18,"roles":1796,"affiliations":1797,"properties":1806,"displayName":1808,"givenName":18,"familyName":18},"e80c0862-8f49-47cd-bc3f-aa0a9f0e91fe",[88],[1798],{"id":1799,"sortIndex":19,"affiliation":1800,"properties":18},"ae1ff4c9-c6ee-4e3a-9884-1066df4da2a4",{"id":1799,"createTime":18,"updateTime":18,"relativeEntities":1801,"slug":18,"properties":1802,"entityType":18,"verifyStatus":18,"verifyTime":18,"verifyNote":18,"languages":18,"translateLanguages":18,"viewCount":18,"url":18,"parentIds":1805,"statistic":18},[],{"title":1803},{"VI":1804},"Department of Surgery, Japan Community Health Care Organization Kumamoto General Hospital, Yatsushiro, 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treatment options for lymphatic malformations (LMs) are multimodal. Recently, the effectiveness of treating LMs with Eppikajyutsuto (TJ-28) has been reported. TJ-28 is a kind of oral herbal medicine classified as the traditional Japanese Kampo medicine. A 12-year-old girl was admitted to our hospital for intermittent upper abdominal pain. Radiological examinations revealed a large (9.5 × 5.8 × 10.0 cm) retroperitoneal LM, which was suspected to adhering and stretching both pancreas head and duodenum. The large retroperitoneal tumor resection might induce involving complications because of the size and the location. Therefore, we used TJ-28 in order to diminish the tumor size before surgery. The patient received oral doses of 7.5 g\u002Fday (2.5 g × 3 times\u002Fday) of TJ-28. Six months after the medication, the tumor decreased markedly to 3.5 × 1.5 × 1.2 cm in size. Thereafter, the mass was sub-totally resected (95%) via a 3 cm trans-umbilical incision without any surgical complications. We reported a case of successfully treated retroperitoneal LM with the combination treatment of TJ-28 and surgery. Based on our experience, this TJ-28 treatment option may be very useful in treating cases of LMs having surgical difficulties because of size and\u002For location.",{"EN":1958},"A large retroperitoneal lymphatic malformation successfully treated with traditional Japanese Kampo medicine in combination with surgery",{"VOID":1566},{"VOID":1961},"Kulungowski AM, Fishman SJ. Chapter 125. Vascular anomalies. In: Coran A, editor. Pediatric Surgery. 7th ed. New York, NA: Saunders; 2012. p. 1621–4.\nBagrodia N, Defnet AM, Kandel JJ. Management of lymphatic malformations in children. Curr Opin Pediatr. 2015;27:356–63. doi:10.1097\u002FMOP.0000000000000209.\nHorbach SE, Jolink F, van der Horst CM. Oral sildenafil as a treatment option for lymphatic malformations in PIK3CA-related tissue overgrowth syndromes. Dermatol Thera. 2016;29:466–9. doi:10.1111\u002Fdth.12398.\nOzeki M, Fukao T, Kondo N. Propranolol for intractable diffuse lymphangioma. N Engl J Med. 2011;364:1380–2. doi:10.1056\u002FNEJMc1013217.\nMcCormick A, Rosenberg S, Trier K, et al. A case of a central conducting lymphatic anomaly responsive to sirolimus. Pediatrics. 2016; 137: doi: 10.1542\u002Fpeds.2015-2694.\nVlahovic AM, Vlahovic NS, Haxhija EQ. Sirolimus for the treatment of a massive capillary-lymphatico-venous malformation: a case report. Pediatrics. 2015;136:e513–6. doi:10.1542\u002Fpeds.2014-3469.\nOgawa-Ochiai K, Sekiya N, Kasahara Y, et al. A case of mediastinal lymphangioma successfully treated with Kampo medicine. J Altern Complement Med. 2011;17:563–5. doi:10.1089\u002Facm.2010.0562.\nHashizume N, Yagi M, Egami H, et al. Clinical efficacy of herbal medicine for pediatric lymphatic malformations: a pilot study. Pediatr Dermatol. 2016;33:191–5. doi:10.1111\u002Fpde.12777.\nKasahara Y, Hikino H, Tsurufuji S, et al. Antiinflammatory actions of ephedrines in acute inflammations. Planta Med. 1985;51:325–31.\nMatsuo K, Koizumi K, Fujita M, et al. Efficient use of a crude drug\u002Fherb library reveals ephedra herb as a specific antagonist for TH2-specific chemokine receptors CCR3, CCR4 and CCR8. Front Cell Dev Biol. 2016;4:54. doi:10.3389\u002Ffcell.2016.00054.\nAoki K, Yamakuni T, Yoshida M, et al. Ephedorae herba decreases lipoploysaccharide-induced cyclooxgenase-2 protein expression and NF-κB-dependent transcription in C6 rat glioma cells. J Pharmacol Sci. 2005;98:327–30.\nSidle DM, Maddalozzo J, Meier JD, et al. Altered pigment epithelium-derived factor and vascular endothelial growth factor levels in lymphangioma pathogenesis and clinical recurrence. Arch Otolaryngol Head Neck Surg. 2005;131:990–5.\nBrouillard P, Boon L, Vikkula M. Genetics of lymphatic anomalies. 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