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DICER1-pleuropulmonary blastoma familial tumor predisposition syndrome: a unique constellation of neoplastic conditions

机译:DICER1肺肺母细胞瘤家族性肿瘤易感综合征:肿瘤性疾病的独特星座

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摘要

Germline mutations in DICER1 are associated with increased risk for a wide variety of neoplastic conditions, including pleuropulmonary blastoma (PPB), cystic nephroma, nasal chondromesenchymal hamartoma, ovarian Sertoli-Leydig cell tumors, botryoid embryonal rhabdomyosarcoma of the uterine cervix, ciliary body medulloepithelioma, pineoblastoma, pituitary blastoma and nodular thyroid hyperplasia or thyroid carcinoma. These tumors may be seen in isolation or in constellation with other characteristic tumor types in individuals or family members. Here we describe the medical history of a child with a heterozygous, loss of function germline DICER1 mutation and multiple tumors associated with the syndrome.. Although germline mutations in DICER1 are rare, tumors of these types will be seen by practicing pathologists and should prompt consideration of an underlying DICER1 mutation.
机译:DICER1中的种系突变与多种肿瘤性疾病的风险增加相关,包括胸膜肺母细胞瘤(PPB),囊性肾瘤,鼻软骨间质性错构瘤,卵巢Sertoli-Leydig细胞瘤,类葡萄球样胚性横纹肌肉瘤,子宫宫颈,皮样母细胞瘤,垂体母细胞瘤和结节性甲状腺增生或甲状腺癌。在个体或家庭成员中,这些肿瘤可能与其他特征性肿瘤类型分离或与星座相伴。在这里,我们描述了患有杂合子,功能丧失种系DICER1突变以及与该综合征相关的多个肿瘤的儿童的病史。尽管DICER1中的种系突变很少见,但这些类型的肿瘤将由执业病理学家发现,应及时考虑潜在的DICER1突变。

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