| Literature DB >> 20152336 |
Alessia Compostella1, Tiziana Toffolutti, Pietro Soloni, Patrizia Dall'Igna, Modesto Carli, Gianni Bisogno.
Abstract
Fanconi anemia (FA) is an autosomal recessive inherited syndrome characterized by congenital abnormalities, aplastic anemia, and a high likelihood of developing cancer. We describe a child who presented with 2 synchronous solid tumors (Wilms tumor and neuroblastoma), later found to have FA, who developed severe toxicity and died after a first cycle of chemotherapy. Our experience emphasizes that a predisposing genetic condition should be sought in cases of multiple tumors and that managing FA patients with cancer can be particularly difficult. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20152336 DOI: 10.1016/j.jpedsurg.2009.11.015
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545