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Morphology and Immunohistochemistry for 2SC and FH Aid in Detection of Fumarate Hydratase Gene Aberrations in Uterine Leiomyomas From Young Patients.2SC和FH的形态学及免疫组织化学有助于检测年轻患者子宫平滑肌瘤中的延胡索酸水合酶基因异常。
Am J Surg Pathol. 2015 Nov;39(11):1529-39. doi: 10.1097/PAS.0000000000000520.
2
Clear Cell Renal Cell Carcinoma With Borderline Features of Clear Cell Papillary Renal Cell Carcinoma: Combined Morphologic, Immunohistochemical, and Cytogenetic Analysis.具有透明细胞乳头状肾细胞癌边缘特征的透明细胞肾细胞癌:形态学、免疫组织化学和细胞遗传学联合分析
Am J Surg Pathol. 2015 Nov;39(11):1502-10. doi: 10.1097/PAS.0000000000000514.
3
Tubulocystic renal cell carcinoma is an entity that is immunohistochemically and genetically distinct from papillary renal cell carcinoma.管状囊性肾细胞癌在免疫组化和遗传学上有别于乳头状肾细胞癌。
Histopathology. 2016 May;68(6):850-7. doi: 10.1111/his.12840. Epub 2015 Oct 21.
4
PSF/SFPQ is a very common gene fusion partner in TFE3 rearrangement-associated perivascular epithelioid cell tumors (PEComas) and melanotic Xp11 translocation renal cancers: clinicopathologic, immunohistochemical, and molecular characteristics suggesting classification as a distinct entity.PSF/SFPQ 是 TFE3 重排相关血管周上皮样细胞瘤(PEComa)和黑色素性 Xp11 易位肾细胞癌中非常常见的基因融合伙伴:提示分类为独特实体的临床病理、免疫组织化学和分子特征。
Am J Surg Pathol. 2015 Sep;39(9):1181-96. doi: 10.1097/PAS.0000000000000502.
5
Clear cell papillary renal cell carcinoma and renal angiomyoadenomatous tumor: two variants of a morphologic, immunohistochemical, and genetic distinct entity of renal cell carcinoma.透明细胞乳头状肾细胞癌和肾血管肌腺瘤样肿瘤:肾细胞癌一种形态学、免疫组化及遗传学特征独特的实体的两种变体。
Am J Surg Pathol. 2015 Jul;39(7):889-901. doi: 10.1097/PAS.0000000000000456.
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Clear cell-papillary renal cell carcinoma of the kidney not associated with end-stage renal disease: clinicopathologic correlation with expanded immunophenotypic and molecular characterization of a large cohort with emphasis on relationship with renal angiomyoadenomatous tumor.不伴有终末期肾病的肾透明细胞乳头状肾细胞癌:与一大组病例扩展的免疫表型及分子特征的临床病理相关性,重点关注与肾血管肌腺瘤的关系
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A Novel SDHA-deficient Renal Cell Carcinoma Revealed by Comprehensive Genomic Profiling.全面基因组分析揭示的一种新型 SDHA 缺陷型肾细胞癌。
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Recurrent epimutation of SDHC in gastrointestinal stromal tumors.胃肠道间质瘤中SDHC的复发性表观突变
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Acquired cystic disease-associated renal cell carcinoma with a focal sarcomatoid component: Report of a case showing more pronounced polysomy of chromosomes 3 and 16 in the sarcomatoid component.获得性囊性疾病相关性肾细胞癌伴局灶性肉瘤样成分:1例报告,显示肉瘤样成分中3号和16号染色体多倍体更为明显。
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Thyroid-like follicular renal cell carcinoma: an emerging morphological variant.甲状腺样滤泡性肾细胞癌:一种新出现的形态学变异型。
Pathology. 2014 Dec;46(7):657-60. doi: 10.1097/PAT.0000000000000176.

罕见及近期报道的肾细胞癌的分子遗传学与免疫组织化学特征

Molecular genetics and immunohistochemistry characterization of uncommon and recently described renal cell carcinomas.

作者信息

Rao Qiu, Xia Qiu-Yuan, Cheng Liang, Zhou Xiao-Jun

机构信息

1 Department of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China ; 2 Department of Pathology and Laboratory, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Chin J Cancer Res. 2016 Feb;28(1):29-49. doi: 10.3978/j.issn.1000-9604.2016.01.03.

DOI:10.3978/j.issn.1000-9604.2016.01.03
PMID:27041925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4779753/
Abstract

Renal cell carcinoma (RCC) compromises multiple types and has been emerging dramatically over the recent several decades. Advances and consensus have been achieved targeting common RCCs, such as clear cell carcinoma, papillary RCC and chromophobe RCC. Nevertheless, little is known on the characteristics of several newly-identified RCCs, including clear cell (tubulo) papillary RCC, Xp11 translocation RCC, t(6;11) RCC, succinate dehydrogenase (SDH)-deficient RCC, acquired cystic disease-associated RCC, hereditary leiomyomatosis RCC syndrome-associated RCC, ALK translocation RCC, thyroid-like follicular RCC, tubulocystic RCC and hybrid oncocytic/chromophobe tumors (HOCT). In current review, we will collect available literature of these newly-described RCCs, analyze their clinical pathologic characteristics, discuss their morphologic and immunohistologic features, and finally summarize their molecular and genetic evidences. We expect this review would be beneficial for the understanding of RCCs, and eventually promote clinical management strategies.

摘要

肾细胞癌(RCC)有多种类型,在最近几十年中显著增多。针对常见的肾细胞癌,如透明细胞癌、乳头状肾细胞癌和嫌色性肾细胞癌,已经取得了进展并达成了共识。然而,对于几种新发现的肾细胞癌的特征,包括透明细胞(小管)乳头状肾细胞癌、Xp11易位性肾细胞癌、t(6;11)肾细胞癌、琥珀酸脱氢酶(SDH)缺陷型肾细胞癌、获得性囊性疾病相关性肾细胞癌、遗传性平滑肌瘤病肾细胞癌综合征相关性肾细胞癌、ALK易位性肾细胞癌、甲状腺样滤泡性肾细胞癌、肾小管囊性肾细胞癌和混合性嗜酸性细胞/嫌色性肿瘤(HOCT),人们了解甚少。在本综述中,我们将收集这些新描述的肾细胞癌的现有文献,分析它们的临床病理特征,讨论它们的形态学和免疫组织化学特征,最后总结它们的分子和遗传学证据。我们期望本综述将有助于对肾细胞癌的理解,并最终促进临床管理策略的发展。