Rhabdomyosarcoma-Associated Renal Cell Carcinoma: A Link with Constitutional TP53 Mutation

被引:8
作者
Curry, Sarah [2 ]
Ibrahim, Fadi [3 ]
Grehan, David [1 ]
Mcdermott, Michael [1 ]
Capra, Michael [2 ]
Betts, David [4 ]
O'Sullivan, Maureen [1 ]
机构
[1] Our Ladys Childrens Hosp, Dept Pathol, Dublin, Ireland
[2] Our Ladys Childrens Hosp, Dept Oncol, Dublin, Ireland
[3] Our Ladys Childrens Hosp, Dept Surg, Dublin, Ireland
[4] Our Ladys Childrens Hosp, Dept Genet, Dublin, Ireland
关键词
constitutional predisposition; renal cell carcinoma; rhabdomyosarcoma; second malignancy; P53; NEUROBLASTOMA; TRANSLOCATION; UNCOMMON; SUBTYPES; CANCER;
D O I
10.2350/10-07-0871-CR.1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The 2004 World Health Organization classification includes the new entity "neuroblastoma-associated renal cell carcinoma." The pathogenetic link between these entities is unknown as yet. The patient reported herein developed renal cell carcinoma after anaplastic embryonal rhabdomyosarcoma, a previously unknown association. The 2nd malignancy developed very soon after the 1st one, prompting concern for inherent cancer predisposition rather than a therapy-induced 2nd malignancy. A variety of features raised suspicion for Tp53 mutation, and indeed a pathogenic germline Tp53 mutation was identified in this child, despite a negative family history for Li-Fraumeni syndrome. Consideration of underlying predisposition is advocated in the context of rapid evolution of 2nd childhood malignancy.
引用
收藏
页码:248 / 251
页数:4
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