Literature DB >> 20152336

Multiple synchronous tumors in a child with Fanconi anemia.

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.

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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


  8 in total

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4.  The Cellular and Molecular Landscape of Synchronous Pediatric Sialoblastoma and Hepatoblastoma.

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5.  Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia.

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7.  Immune Checkpoint Inhibition as Single Therapy for Synchronous Cancers Exhibiting Hypermutation: An IRRDC Study.

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  8 in total

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