生殖系
医学
遗传倾向
李-弗劳门尼综合征
癌症
种系突变
遗传性癌症
基因检测
病理
肾上腺皮质癌
人类遗传学
癌症遗传学
免疫组织化学
遗传咨询
生物信息学
遗传性疾病
分子病理学
分子诊断学
小儿癌症
癌
作者
Vânia Nosé,Şule Canberk,Abbas Agaimy
标识
DOI:10.1097/pap.0000000000000545
摘要
Germline predisposition contributes to at least 10% of human malignancies and is identified in ∼8.5% to 10% of pediatric cancers, with notably higher frequencies in specific tumor types, including over 60% in adrenocortical carcinoma and 17% to 20% in osteosarcoma. In certain tumors, hereditary predisposition is a defining or highly characteristic feature. Advances in next-generation sequencing have significantly reshaped our understanding of hereditary tumor biology, revealing molecularly distinct neoplasms linked by shared germline alterations and enabling the recognition of new cancer predisposition syndromes. This evolving knowledge is reflected in the WHO Classification of Tumors: Genetic Tumor Syndromes, which provides an integrated, cross-disciplinary diagnostic framework. Surgical pathologists play a central role in this landscape. Careful morphologic assessment, supported by targeted immunohistochemistry and clinical context, often allows the pathologist to identify features of germline predisposition-sometimes as the first or only clinician to do so, even in the absence of a relevant family history. This review highlights 13 practical morphologic and clinicopathological clues that should prompt consideration of a hereditary tumor syndrome, summarizes key immunohistochemical tools for syndromic triage, and presents an organ-based overview of major hereditary cancer syndromes. The goal is to provide a practical framework to support the pathologist's role in recognizing hereditary cancer.
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