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Studies that emphasize important diagnostic and prognostic features involving human tissue provide the basis for publication of works utilizing standard techniques, as well as those from applied and basic science. 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The patient usually presents with nonspecific symptoms and a remarkable deterioration in performance status. The occurrence of synchronous IVLBCL and renal cell carcinoma (RCC) is extremely rare. A right kidney tumor was found in a 72-year-old man with a history of low back pain. The kidney was enlarged, with a tumor mass measuring 4.5 × 4 × 4 cm. Sections exhibited a RCC (clear cell type, nuclear grade I). Also an extensive tumor affecting capillaries and small veins was present, positive for CD45, CD20, BCL-2, and MUM1\u002FIRF-4, consistent with IVLBCL. The lymphoma was circumscribed to the RCC. The final diagnosis was IVLBCL with a RCC as collision tumor. After that, with neurological findings, central nervous system compromise by lymphoma was made. The patient started a first cycle of chemotherapy, progressive deterioration of the sensorium, and positive blood cultures for Klebsiella pneumoniae and Escherichia coli. The patient died 8 days later of acute respiratory failure. No autopsy was done. IVLBCL is an aggressive and systemic disease characterized by massive proliferation of tumor cells without a known primary site. Clinical identification and histopathologic diagnosis are relevant issues in the therapeutic management of these lymphomas. Until now, only one case of IVLBCL coexisting with RCC has been reported. In this article, we report a second case of IVLBCL with RCC simultaneous, as an unusual collision tumor. \u003C\u002Fjats:p>",{"EN":147},"Intravascular Large B-Cell Lymphoma and Renal Clear Cell Carcinoma as Collision Tumor: A Case Report and Review of the Literature",{"VOID":149},"33345662",{"VOID":151},"10.1177\u002F1066896920981633","PUBLICATION","VERIFIED","Auto 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Diffuse large B-cell lymphoma. In: Jaffe E, Arber D, Campo E, eds. Hematopathology. 2nd ed. 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We reviewed the cases of endometriosis of soft tissue sites seen at a tertiary soft tissue center. All cases of extra-abdominal soft tissue endometriosis diagnosed at this institution over a 13-year period were reviewed, and clinical and pathologic findings were recorded. Forty-five patients had diagnoses of soft tissue endometriosis and there were 34 diagnostic biopsies and 26 surgical excision specimens. All but 1 case were abdominal wall lesions, with 1 located in the upper arm. A total of 33 patients presented with lesions in scars of previous operations (31 in Pfannenstiel incisions for Caesarean sections, presenting with a median interval of 6 years (range 1-16 years) following surgery). The lesions ranged in size from 1 to 8 cm (median 3.5 cm). One case showed decidualized stroma with trophoblast cells, while 2 had secondary adenocarcinoma arising from endometriosis. Eighteen cases were tested for β-catenin expression immunohistochemically, of which 5 showed at least focal nuclear positivity in the surrounding fibrous tissue (although not within glands or stroma). Soft tissue endometriosis is seen most commonly in surgical scars, particularly following Caesarean sections. Spontaneous endometriosis also most commonly occurs in the abdominal wall, although can occur exceptionally at unusual sites, such as extremities. Secondary changes, including carcinomas, can arise from endometriosis. The differential diagnosis of these lesions includes fibromatosis, which may be erroneously diagnosed on small, nonrepresentative core biopsy specimens. \u003C\u002Fjats:p>",{"EN":369},"Endometriosis of Extra-Abdominal Soft Tissues",{"VOID":371},"27098587",{"VOID":373},"10.1177\u002F1066896916644322",[156],"https:\u002F\u002Fjournals.sagepub.com\u002Fdoi\u002F10.1177\u002F1066896916644322",[377,399,416,433],{"id":378,"sortIndex":25,"researcher":24,"roles":379,"affiliations":380,"properties":392},"10e71947-e961-4d57-a039-4bf169233eca",[],[381],{"id":382,"sortIndex":25,"affiliation":383,"properties":24},"49dd5c58-0583-4987-8d9e-52a540cd1ef0",{"id":384,"createTime":385,"updateTime":386,"relativeEntities":387,"slug":388,"properties":389,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"7fd45094-212b-4ca6-b8a8-4a14b29cf9eb","2023-12-18T01:02:46.721+00:00","2024-12-25T00:05:58.214+00:00",[],"Royal-Marsden-Hospital-London-UK",{"title":390},{"VI":391},"Royal Marsden Hospital, London, UK",{"openalex":393,"orcid":395,"title":397},{"VOID":394},"A5102793149",{"VOID":396},"https:\u002F\u002Forcid.org\u002F0000-0001-8638-7506",{"EN":398},"Jayson Wang",{"id":400,"sortIndex":113,"researcher":24,"roles":401,"affiliations":402,"properties":409},"c2c50021-deca-48c5-a65c-da4d1abb8fea",[],[403],{"id":404,"sortIndex":25,"affiliation":405,"properties":24},"9da19be0-cc84-4be1-ba4d-59c6c29559f9",{"id":384,"createTime":385,"updateTime":386,"relativeEntities":406,"slug":388,"properties":407,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":408},{"VI":391},{"openalex":410,"orcid":412,"title":414},{"VOID":411},"A5048179253",{"VOID":413},"https:\u002F\u002Forcid.org\u002F0000-0002-0557-9379",{"EN":415},"Christina Messiou",{"id":417,"sortIndex":111,"researcher":24,"roles":418,"affiliations":419,"properties":426},"6e51bd95-b080-469d-a8ec-e7320c18b2be",[],[420],{"id":421,"sortIndex":25,"affiliation":422,"properties":24},"70c1a320-9290-4a74-a8a6-4bb6a0ca2cd3",{"id":384,"createTime":385,"updateTime":386,"relativeEntities":423,"slug":388,"properties":424,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":425},{"VI":391},{"openalex":427,"orcid":429,"title":431},{"VOID":428},"A5046385124",{"VOID":430},"https:\u002F\u002Forcid.org\u002F0000-0001-9727-8030",{"EN":432},"Khin Thway",{"id":434,"sortIndex":115,"researcher":24,"roles":435,"affiliations":436,"properties":443},"6464ae9e-3881-4041-a92b-fe7c89396a82",[],[437],{"id":438,"sortIndex":25,"affiliation":439,"properties":24},"d911199a-6f13-42d2-a207-4450608f15a4",{"id":384,"createTime":385,"updateTime":386,"relativeEntities":440,"slug":388,"properties":441,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":442},{"VI":391},{"openalex":444,"orcid":446,"title":448},{"VOID":445},"A5059717371",{"VOID":447},"https:\u002F\u002Forcid.org\u002F0000-0003-2413-0697",{"EN":449},"D. 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Desmoplastic small round cell tumor (DSRCT) is an aggressive round cell sarcoma that arises in the abdominal cavity\u002Fpelvis of young males. We sought to expand its clinicopathologic spectrum. Methods. Cases of DSRCT presenting in patients >30 years of age or tumors arising outside of the abdominal cavity\u002Fpelvis were retrieved. Results. Thirty-four cases were identified. Sixteen tumors arose at atypical sites (head\u002Fneck, intracranial, thigh, axilla\u002Fshoulder, inguinal\u002Fparatesticular, intraosseous, and uterine corpus). The remaining 18 patients were older than 30 years, and their tumors involved the abdomen or pelvis. The majority of cases showed areas with classic histology, while 6 cases exhibited solid growth and 5 showed macronodular architecture. Cytologic appearance included round cell, rhabdoid, epithelioid, and small cell. Conclusion. 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It most often occurs in the genitourinary tract; however, isolated cases have been reported in many other organs, including colon, stomach, lung, liver, bone, uterus, and skin. In the bladder, which is the most common site of involvement, it may be mistaken for malignancy on cystoscopic examination or computerized topography scan. Gram-negative bacteria such as Escherichia coli and Klebsiella pneumonia are often isolated from malakoplakia lesions, although other less common bacteria such as Rhodococcus equi may also be found. This is a case report of prostatic malakoplakia diagnosed on needle core biopsy from a patient suspected to harbor a malignancy. \u003C\u002Fjats:p>",{"EN":1223},"Malakoplakia of the Prostate on Needle Core Biopsy: A Case Report and Review of the Literature",{"VOID":1225},"17172507",{"VOID":1227},"10.1177\u002F1066896906295892",[156],"https:\u002F\u002Fjournals.sagepub.com\u002Fdoi\u002F10.1177\u002F1066896906295892",[1231,1251,1271,1288],{"id":1232,"sortIndex":25,"researcher":24,"roles":1233,"affiliations":1234,"properties":1246},"19bae96b-a523-4d35-b45e-5ae0de609ee1",[],[1235],{"id":1236,"sortIndex":25,"affiliation":1237,"properties":24},"9994ece6-5c6c-48b4-be0d-eca93da327a5",{"id":1238,"createTime":1239,"updateTime":1240,"relativeEntities":1241,"slug":1242,"properties":1243,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"9c1620f2-e755-4662-87cc-447f350413ee","2023-11-26T22:46:54.131+00:00","2024-10-08T11:17:11.306+00:00",[],"Departments-of-Pathology-and-Laboratory-Medicine-University-of-Rochester-Medical-Center-Rochester-New-York",{"title":1244},{"VI":1245},"Departments of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York",{"openalex":1247,"title":1249},{"VOID":1248},"A5105973935",{"EN":1250},"David G. 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L, 1902, Zeitschrift fur klinische Medizin., 47, 208",{},{"id":24,"text":1352,"url":24,"identifiers":1353},"von Hansemann D., 1903, Virchows Archivfurpathologische Anatomie., 173, 302",{},{"id":24,"text":1355,"url":24,"identifiers":1356},"Damjanov I, 1981, Pathol Annu., 6, 103",{},{"id":24,"text":1358,"url":24,"identifiers":1359},"10.1378\u002Fchest.115.3.889",{"doi":1358},{"id":24,"text":1361,"url":24,"identifiers":1362},"Carruthers NC., 1959, Can J Surg., 2, 213",{},{"id":24,"text":1364,"url":24,"identifiers":1365},"Sencer O, 1979, Arch Pathol Lab Med., 103, 446",{},{"id":24,"text":1367,"url":24,"identifiers":1368},"Darvishian F, 2001, Ann Clin Lab Sci., 31, 147",{},{"id":24,"text":1370,"url":24,"identifiers":1371},"Oppenheimer JR, 1997, Arch of Pathol Lab Med., 121, 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Acute interstitial nephritis is commonly seen in kidney biopsies of patients with acute renal failure; however, granulomatous interstitial nephritis (GIN) is rare. We identified 46 cases of GIN in a 17-year period in this institution and we investigated their most probable etiologies. Complete clinical information was available in 38 patients. Seventeen of 38 patients (44.7%) were classified as drug-induced. Renal sarcoidosis was responsible for 28.9% of cases, and the remaining 15.9% of cases included Wegeners granulomatosis, foreign body giant cell reaction, GIN secondary to intravesical bacillus Calmette-Guerin therapy for bladder cancer, and xanthogranulomatous pyelonephritis. Clinical investigation failed to reveal possible etiology in 4 patients (10.5%), classified as idiopathic. We concluded that three quarters of our cases were either drug-induced or due to sarcoidosis; only a small proportion of our cases occurred secondary to any other cause or to unknown factors. \u003C\u002Fjats:p>",{"EN":1407},"Granulomatous Interstitial Nephritis: A Clinicopathologic Study of 46 Cases from a Single Institution",{"VOID":1409},"16501836",{"VOID":1411},"10.1177\u002F106689690601400110","Author affiliation is blank",[156],"https:\u002F\u002Fjournals.sagepub.com\u002Fdoi\u002F10.1177\u002F106689690601400110",[1416,1445,1462,1473],{"id":1417,"sortIndex":25,"researcher":24,"roles":1418,"affiliations":1419,"properties":1440},"a170d4d6-6be7-4b75-b85f-a6b0fb43657a",[],[1420,1430],{"id":1421,"sortIndex":25,"affiliation":1422,"properties":24},"2157af40-2d69-42a6-83da-91390cfec46b",{"id":1423,"createTime":1424,"updateTime":1424,"relativeEntities":1425,"slug":1426,"properties":1427,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"80f44f5f-3df4-4c3b-a9d8-11cb95821fc5","2024-09-22T10:06:00.858+00:00",[],"Department-of-Pathology-Brigham-and-Womens-Hospital-Harvard-Medical-School-Boston-MA",{"title":1428},{"EN":1429},"Department of Pathology, Brigham and Womens Hospital-Harvard Medical School, Boston, MA",{"id":1431,"sortIndex":115,"affiliation":1432,"properties":24},"445a1b41-c5c1-4522-a551-862151c4dfec",{"id":1433,"createTime":1434,"updateTime":1434,"relativeEntities":1435,"slug":1436,"properties":1437,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"b7944444-682d-487d-94ec-2652511cd4c3","2024-09-22T10:06:00.861+00:00",[],"Department-of-Pathology-Brigham-and-Womens-Hospital-Harvard-Medical-School-Boston-MA-Pathology-and-Lab-Medicine-Emory-University-EUH-H188-1364-Clifton-Road-NE-Atlanta-GA-30322",{"title":1438},{"EN":1439},"Department of Pathology, Brigham and Womens Hospital-Harvard Medical School, Boston, MA; Pathology and Lab Medicine, Emory University EUH, H188, 1364 Clifton Road NE, Atlanta, GA 30322",{"openalex":1441,"title":1443},{"VOID":1442},"A5027528681",{"EN":1444},"Vanesa Bijol",{"id":1446,"sortIndex":111,"researcher":24,"roles":1447,"affiliations":1448,"properties":1455},"19ea4afb-4156-4c5f-b952-572706bc7e81",[],[1449],{"id":1450,"sortIndex":25,"affiliation":1451,"properties":24},"96e5724b-45d2-4a1c-8f48-31b88c0b317a",{"id":1423,"createTime":1424,"updateTime":1424,"relativeEntities":1452,"slug":1426,"properties":1453,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":1454},{"EN":1429},{"openalex":1456,"orcid":1458,"title":1460},{"VOID":1457},"A5013889724",{"VOID":1459},"https:\u002F\u002Forcid.org\u002F0000-0001-6442-3465",{"EN":1461},"Helmut G. 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Malignant extragonadal germ cell tumors primary to the lung are quite uncommon lesions, but pure yolk sac tumor is even more exceptional. This is believed to be the first reported case of yolk sac tumor of the lung in which an intense and diffuse immunoreactivity for CDX2, a marker of intestinal differentiation reportedly expressed also in gonadal yolk sac tumor, was associated with increased serum levels of the alkaline phosphatase intestinal isoform. Nine months after radical surgery and adjuvant chemotherapy, the patient is alive and well without evidence of recurrent or metastatic disease and with serum levels of the alkaline phosphatase intestinal isoform within normal limits. 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CDX2 has been detected in the majority of colorectal adenocarcinoma cases and may be useful in determining the sites of origin of tumors. In this study, the authors evaluated CDX2 expression in germ cell tumors (GCTs) by immunohistochemistry. Forty cases of testicular GCTs and 8 cases of metastatic GCTs were retrieved for study. In the 40 cases of testicular GCTs, 13 were pure seminomas and 27 mixed GCTs. Yolk sac tumor (YST) was identified by morphology and glypican 3 staining in 20 testicular mixed GCTs. Of these 20 cases, 8 cases showed 1+ positivity for CDX2. Other primitive components of GCTs were negative. For the 6 cases of metastatic mixed GCT with YST, 4 cases were positive, 2+ in 2 cases and 1+ in 2 cases. 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Ectopic adrenal cortical neoplasms are extremely rare, and only a few have involved the CNS. We report the first case of an intramedullary oncocytic adrenal cortical neoplasm of the spinal cord with immunohistochemical (IMHC) confirmation. A 27-year-old man presented with progressive lower extremity weakness, spastic paraparesis, decreased reflexes, and hypoesthesia below T10. A spinal myelogram showed cauda equina blockade and obliteration of sacral nerve roots. This prompted emergent surgical intervention. A well-circumscribed, approximately 3 × 2 cm, light brown to tan, intramedullary tumor was identified at the level of the conus medullaris. Histologically, the tumor showed sheets and nests of plump, cytologically bland polygonal cells with abundant eosinophilic cytoplasm. A single mitosis, but no necrosis, was identified. By IMHC, the cells were positive for inhibin, melan-A, and synaptophysin, and negative for GFAP, EMA, cytokeratins, S-100, HMB-45, and chromogranin. Electron microscopy study performed from paraffin-embedded tissues demonstrated abundant mitochondria, and lipid vacuoles. This case confirms the occurrence of adrenal cortical neoplasms in the CNS and is the first report of an intradural, intramedullary adrenal cortical adenoma of the spinal cord, and the first to occur in a male. This tumor should be considered in the differential diagnosis of tumors of the CNS. \u003C\u002Fjats:p>",{"EN":2030},"Spinal Adrenal Cortical Adenoma with Oncocytic Features: Report of the First Intramedullary Case and Review of the Literature",{"VOID":2032},"15306940",{"VOID":2034},"10.1177\u002F106689690401200309",[156],"https:\u002F\u002Fjournals.sagepub.com\u002Fdoi\u002F10.1177\u002F106689690401200309",[2038,2057,2076,2097,2116,2138,2160],{"id":2039,"sortIndex":111,"researcher":24,"roles":2040,"affiliations":2041,"properties":2052},"6bd8dcb2-2b50-4cdd-92e6-0d1505a26c77",[],[2042],{"id":2043,"sortIndex":25,"affiliation":2044,"properties":24},"666c3e9d-ef55-422e-8464-6110643df64d",{"id":2045,"createTime":2046,"updateTime":2046,"relativeEntities":2047,"slug":2048,"properties":2049,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"63ab303a-fef9-4672-bba0-fdf7e0118569","2025-02-03T05:42:01.064+00:00",[],"Biopse-Laboratories-Ceara-Brazil",{"title":2050},{"EN":2051},"Biopse Laboratories, Ceara, Brazil",{"openalex":2053,"title":2055},{"VOID":2054},"A5111619635",{"EN":2056},"Régia Maria do Socorro Vidal Patrocínio",{"id":2058,"sortIndex":115,"researcher":24,"roles":2059,"affiliations":2060,"properties":2071},"a8acf571-9d7d-4d5c-9acc-cdbae8c27842",[],[2061],{"id":2062,"sortIndex":25,"affiliation":2063,"properties":24},"f49fce45-3a14-4699-aa0a-45a3ad84956c",{"id":2064,"createTime":2065,"updateTime":2065,"relativeEntities":2066,"slug":2067,"properties":2068,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"35bd803f-d59f-4b52-a2d5-6be156c55393","2025-02-03T05:42:00.988+00:00",[],"Department-of-Pathology-Washington-Children-s-Hospital-Washington-DC",{"title":2069},{"EN":2070},"Department of Pathology, Washington Children’s Hospital, Washington DC",{"openalex":2072,"title":2074},{"VOID":2073},"A5108395090",{"EN":2075},"Mariarita Santi",{"id":2077,"sortIndex":113,"researcher":24,"roles":2078,"affiliations":2079,"properties":2090},"2ef452b3-75dd-4c7d-b250-4c6cd3c5c3d9",[],[2080],{"id":2081,"sortIndex":25,"affiliation":2082,"properties":24},"63173bfb-03a1-4eac-9703-7b58fd77918e",{"id":2083,"createTime":2084,"updateTime":2084,"relativeEntities":2085,"slug":2086,"properties":2087,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"29b98e6c-83b8-4bd3-beab-2e3e46d6d14c","2025-02-03T05:42:01.011+00:00",[],"Department-of-Surgery-Hospital-Das-Clinicas-Ceara-Brazil",{"title":2088},{"EN":2089},"Department of Surgery, Hospital Das Clinicas, Ceara Brazil",{"openalex":2091,"orcid":2093,"title":2095},{"VOID":2092},"A5058808837",{"VOID":2094},"https:\u002F\u002Forcid.org\u002F0000-0001-7694-9624",{"EN":2096},"Arnaldo Ribeiro de Arruda",{"id":2098,"sortIndex":110,"researcher":24,"roles":2099,"affiliations":2100,"properties":2111},"76236694-d1c0-4a45-9eba-e1a0af596656",[],[2101],{"id":2102,"sortIndex":25,"affiliation":2103,"properties":24},"99adb716-b284-422e-bf62-7649e60877ef",{"id":2104,"createTime":2105,"updateTime":2105,"relativeEntities":2106,"slug":2107,"properties":2108,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"4b4c6c22-36dc-4955-ba5c-7ab958ac866b","2025-02-03T05:42:01.190+00:00",[],"Neuropathology-and-Autopsy-Service-MCV-Hospitals-Virginia-Commonwealth-University-Richmond-VA",{"title":2109},{"EN":2110},"Neuropathology and Autopsy Service, MCV Hospitals, Virginia Commonwealth University, Richmond, VA",{"openalex":2112,"title":2114},{"VOID":2113},"A5087643619",{"EN":2115},"Nitya R. 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oncocytomas of uncertain malignant potential, and 4 oncocytic carcinomas. Histologically all tumors were entirely or predominantly composed of oncocytes. Immunohistochemically all tumors were immunoreactive for mitochondrial antigen mES-13. Electron microscopy was performed in 8 cases and was confirmatory of the oncocytic cell change. The morphologic parameters of the Weiss system, considered to be predictive of the biologic behavior of conventional (nononcocytic) adrenocortical tumors, are reviewed in the context of their possible application to the oncocytic tumor variant. Proposed major criteria (high mitotic rate, atypical mitoses, venous invasion) and minor criteria (large size and huge weight, necrosis, capsular invasion, sinusoidal invasion) in distinguishing malignant tumors are discussed, and definitional criteria (predominantly cells with eosinophilic and granular cytoplasm, high nuclear grade, diffuse architectural pattern) in common with all types of oncocytic tumors are outlined. The authors’ proposed working rules for diagnostic categorization of oncocytic adrenocortical tumors are defined, with the presence of 1 major criterion indicating malignancy, 1 to 4 minor criteria indicating uncertain malignant potential (borderline), and the absence of all major and minor criteria indicative of benignancy. Using these criteria, the diagnosis of malignancy was straightforward in 3 of the 4 cases designated as oncocytic carcinoma (presence of at least 2 major criteria and all the minor criteria), while in 1 case the original diagnosis of benign oncocytoma was reversed to malignant following critical review of the original pathologic material after local tumor recurrence. Tumor recurrence occurred in 2 carcinomas at 8 and 20 months, respectively, and was followed in 1 case by the patient’s death. The third patient expired at 6 months from unrelated causes, and the fourth patient is free of disease at the relatively short follow-up interval of 6 months. Regarding the 4 patients with borderline tumors, all are alive with no evidence of disease, with follow-up ranging from 10 to 61 months (mean 38.7 months). The 2 benign tumors have a follow-up of 25 and 30 months, respectively. Diagnostic difficulties are delineated and a complete review of the literature on this topic has also been performed.\u003C\u002Fjats:p>",{"EN":2270},"Adrenocortical Oncocytic Tumors: Report of 10 Cases and Review of the Literature",{"VOID":2272},"15306935",{"VOID":2274},"10.1177\u002F106689690401200304",[156],"https:\u002F\u002Fjournals.sagepub.com\u002Fdoi\u002F10.1177\u002F106689690401200304",[2278,2298,2317,2336,2357,2378,2398,2419],{"id":2279,"sortIndex":487,"researcher":24,"roles":2280,"affiliations":2281,"properties":2293},"45ec9306-6b84-4e9e-b12c-de7332e5922c",[],[2282],{"id":2283,"sortIndex":25,"affiliation":2284,"properties":24},"05585516-275a-44f8-bfe5-429d208e7f21",{"id":2285,"createTime":2286,"updateTime":2287,"relativeEntities":2288,"slug":2289,"properties":2290,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"e0d57f4e-c349-4fb9-9138-5c6c307cdd30","2024-02-09T04:24:41.650+00:00","2025-02-03T05:42:00.113+00:00",[],"Department-of-Pathology-City-of-Hope-National-Medical-Center-Duarte-California-USA",{"title":2291},{"VI":2292},"Department of Pathology, City of Hope National Medical Center, Duarte, California, USA",{"openalex":2294,"title":2296},{"VOID":2295},"A5112182874",{"EN":2297},"Lawrence M. 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