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Chromophobe hepatocellular carcinoma with abrupt anaplasia: a proposal for a new subtype of hepatocellular carcinoma with unique morphological and molecular features

机译:带有不典型增生的生色性肝细胞癌:一种具有独特形态和分子特征的新型肝细胞癌亚型的提议

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Hepatocellular carcinomas exhibit heterogeneous morphologies by routine light microscopy. Although some morphologies represent insignificant variations in growth patterns, others may represent unrecognized subtypes of hepatocellular carcinoma. Identification of these subtypes could lead to separation of hepatocellular carcinomas into discrete groups with unique underlying genetic changes, prognosis, or therapeutic responses. In order to identify potential subtypes, two pathologists independently screened a cohort of 219 unselected hepatocellular carcinoma resection specimens and divided cases into potential subtypes. One of these promising candidate subtypes was further evaluated using histological and molecular techniques. This subtype was characterized by a unique and consistent set of histological features: smooth chromophobic cytoplasm, abrupt focal nuclear anaplasia (small clusters of tumor cells with marked nuclear anaplasia in a background of tumor cells with bland nuclear cytology), and scattered microscopic pseudocysts—we designate this variant as ‘chromophobe hepatocellular carcinoma with abrupt anaplasia’. Thirteen cases were identified (6% of all hepatocellular carcinomas), including 6 men and 7 women with an average age of 61 years. Six cases occurred in cirrhotic livers. Serum AFP was elevated in 6 out of 10 cases. There were a variety of underlying liver diseases, but cases were enrichment for chronic hepatitis B, P=0.006. Interestingly, at the molecular level, this variant was strongly associated with the alternative lengthening of telomere (ALT) phenotype by telomere FISH. ALT is a telomerase-independent mechanism of telomere maintenance and is found in approximately 8% of unselected hepatocellular carcinomas. In contrast, 11/12 (92%) of the cases of chromophobe hepatocellular carcinoma with abrupt anaplasia were ALT-positive. In summary, we propose that chromophobe hepatocellular carcinoma with abrupt anaplasia represents a new subtype of hepatocellular carcinoma with unique morphological and molecular features.
机译:肝细胞癌通过常规光学显微镜表现出异质形态。尽管某些形态代表生长模式的微小变化,但其他形态可能代表无法识别的肝细胞癌亚型。这些亚型的鉴定可能导致肝细胞癌分为具有独特的潜在遗传变化,预后或治疗反应的离散组。为了识别潜在的亚型,两名病理学家独立筛选了219个未经选择的肝细胞癌切除标本的队列,并将病例分为潜在的亚型。使用组织学和分子技术进一步评估了这些有希望的候选亚型之一。该亚型的特点是具有独特且一致的组织学特征:平滑的发色细胞质,突变性局灶性核发育不全(肿瘤细胞呈淡薄小簇,在无核细胞学的肿瘤细胞的背景下具有明显的核发育不良)和散在的显微假性囊肿-我们将这个变体指定为“患有非典型增生的生色性肝细胞癌”。确定了13例病例(占所有肝细胞癌的6%),包括6名男性和7名女性,平均年龄为61岁。肝硬化肝发生6例。每10例中有6例血清AFP升高。有多种潜在的肝脏疾病,但慢性乙型肝炎的病例较多,P = 0.006。有趣的是,在分子水平上,该变体与端粒FISH对端粒(ALT)表型的替代延长密切相关。 ALT是端粒酶维持端粒酶的独立机制,在大约8%的未选肝细胞癌中被发现。相比之下,突然增生的发色性肝细胞癌病例中有11/12(92%)为ALT阳性。综上所述,我们提出伴有不典型增生的生色性肝细胞癌代表了具有独特形态和分子特征的肝细胞癌的新亚型。

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