Results 151 to 160 of about 401,011 (182)

Xp11.2 translocation renal cell carcinoma with NONO-TFE3 gene fusion: morphology, prognosis, and potential pitfall in detecting TFE3 gene rearrangement

Modern Pathology, 2017
Qiu-yuan Xia, Zhe Wang, N. Chen, H. Gan, X. Teng, Shan-Shan Shi, Xuan Wang, Xue Wei, Sheng-bing Ye, Rui Li, Heng-Hui Ma, Zhen-feng Lu, Xiao-jun Zhou, Q. Rao   +13 more
semanticscholar   +1 more source

Adult-onset renal cell carcinoma associated with Xp11.2 translocation/TFE3 gene fusion: 3 case reports and review of literature. [PDF]

Medicine (Baltimore), 2018
Gong P, Zhuang Q, Wang K, Xu R, Chen Y, Wang X, Yin S.   +6 more
europepmc   +1 more source

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Xp11.2 translocation tumor

Journal of the American Academy of Physician Assistants, 2014
Xp11.2 translocation tumor is a rare but aggressive form of renal cell carcinoma that predominantly occurs in children but also may be found in young adults. Because this type of cancer is diagnosed via histologic and chromosomal analysis, clinicians should consider translocation tumor in the differential diagnosis of patients with renal lesions and ...
Howard E, Asaki, Gianni, Moshero, Melissa L, Stanton, Mitchell R, Humphreys   +3 more
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Renal Cell Carcinoma Associated With Xp11.2 Translocations, Report of a Case

Urology, 2010
Renal cell carcinomas (RCCs) associated with Xp11.2 translocations (Xp11.2 translocation RCCs) are rare and occur predominantly in children and adolescents. A case of such tumor in a 12-year boy is reported. Grossly the cut surface of the ill-defined mass was polychromatic, containing areas of hemorrhage and necrosis.
Hongbiao, Jing, Yanhong, Tai, Dazhou, Xu, Fan, Yang, Ming, Geng   +4 more
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Radiologic–pathologic correlation of renal cell carcinoma associated with Xp11.2 translocation

Acta Radiologica, 2013
Background The prognosis of translocation RCCs in adult patients is relatively poor compared to that of other subtypes of RCCs. Although there have been several reports regarding radiologic findings of translocation RCC, studies with histologic correlation could help to understand the imaging features.
Hyun Jung, Koo, Hyuck Jae, Choi, Mi-hyun, Kim, Kyoung-Sik, Cho   +3 more
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Renal Cell Carcinoma with Xp11.2 Translocation in a 7-Year-Old Boy

Klinische Pädiatrie, 2010
More than 90% of pediatric renal tumors are nephroblastomas while renal cell carcinomas (RCC) are rare in children (< 5%).According to the clinical diagnoses of a nephroblastoma stage IV a 7-year-old boy with a kidney tumor and peripheral pulmonary lesion was preoperatively treated for 8 weeks with Vincristine, Actinomycin D and Adriamycin.
C, Jayasinghe, N, Siegler, I, Leuschner, G, Fleischhack, M, Born, A M, Müller   +5 more
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Renal carcinomas associated with Xp11.2 translocations: Are CT findings suggestive of the diagnosis?

Clinical Radiology, 2014
The purpose of the present study was to summarize the computed tomography (CT) features of renal carcinomas associated with Xp11.2 translocations, and determine whether the diagnosis can be reliably deduced from imaging findings.Radiological studies of six patients (aged from 9-29 years) with renal carcinoma associated with Xp11.2 translocations were ...
J, He, Y, Huan, Q, Qiao, J, Zhang, J S, Zhang   +4 more
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Pediatric Renal Cell Carcinoma Associated With Xp11.2 Translocation/TFE3 Gene Fusion

International Journal of Surgical Pathology, 2008
Renal cell carcinoma (RCC) in children and young adults is rare and pathologically problematic. RCC can be either hereditary or sporadic and has a guarded prognosis because appropriate management has not been established. A case of RCC in an 11-year-old is reported.
Ni Wayan, Winarti, Pedram, Argani, Angelo M, De Marzo, Jessica, Hicks, Ketut, Mulyadi   +4 more
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[Research advances in Xp11.2 translocation renal cell carcinoma].

Ai zheng = Aizheng = Chinese journal of cancer, 2010
Xp11.2 translocation renal cell carcinoma (RCC) is a newly identified category of RCC described in the 2004 WHO Classification of Kidney Tumors. Although the incidence is very rare, it accounts about one third of pediatric RCCs. It is different from other RCCs in clinical manifestations, histopathologic features, biological behaviour and prognosis.
Jian-Hua, Huang, Fang-Jian, Zhou
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Long-term outcomes of children with Xp11.2 translocation renal cell carcinoma.

Journal of Clinical Oncology, 2012
9569 Background: We aimed to assess the clinico-pathological characteristics and the long-term prognosis of Xp11.2 translocation renal cell carcinoma (Xp-RCC) in children. Methods: A total of 52 Japanese children with renal tumors were presented to our institutions.
Hiroshi Asanuma, Ryuichi Mizuno, Aya Masuda, Hiroyuki Satoh, Zenichi Matsui, Hidaka Kono, Kazunobu Shinoda, Eiji Kikuchi, Hirohiko Nagata, Akira Miyajima, Ken Nakagawa, Mototsugu Oya   +11 more
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