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澳大利亚家族性肺胸膜胚细胞瘤。

Familial pleuropulmonary blastoma in Australia.

机构信息

Department of Oncology, The Children's Hospital at Westmead, Sydney, Australia.

出版信息

Pediatr Blood Cancer. 2010 Dec 15;55(7):1417-9. doi: 10.1002/pbc.22592.

Abstract

We present three cases of pleuropulmonary blastoma (PPB) in Australian children. Each had a family history of childhood tumors which collectively included PPB, infant lung cyst, cystic nephroma, medullo-epithelioma and a Sertoli-Leydig ovarian tumor. Two of the patients also had additional malignancies: a concurrent bladder rhabdomyosarcoma and a post therapy non-PPB malignant lung tumor. In two cases, the family histories were elicited years after the PPB diagnosis. Archived pathology material allowed revision of pathologic diagnoses from decades earlier. These cases illustrate the importance of detailed inquiry into family medical history and the pleiotropy of the PPB-related familial cancer predisposition syndrome, which appears to result from heterozygous DICER1 mutations.

摘要

我们呈现了三个澳大利亚儿童患有胸膜肺母细胞瘤 (PPB) 的病例。每个病例都有家族史,家族中曾有儿童肿瘤,包括 PPB、婴儿肺囊肿、囊性肾瘤、髓上皮瘤和 Sertoli-Leydig 卵巢肿瘤。其中两名患者还有其他恶性肿瘤:同时患有膀胱横纹肌肉瘤和治疗后非 PPB 恶性肺肿瘤。在两个病例中,家族病史是在 PPB 诊断多年后才发现的。存档的病理学材料允许对几十年前的病理诊断进行修订。这些病例说明了详细询问家族病史的重要性,以及 PPB 相关家族性癌症易感性综合征的多效性,这似乎是由杂合 DICER1 突变引起的。

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