| Literature DB >> 28766837 |
Avi Saskin1,2,3, Leanne de Kock2,3, Nelly Sabbaghian2, Maria Apellaniz-Ruiz2,3, Ceyhun Bozkurt4, Dorothée Bouron-Dal Soglio5, William D Foulkes1,2,3,6.
Abstract
DICER1 syndrome is an inherited disorder associated with at least a dozen rare, mainly pediatric-onset tumors. Its characterization remains incomplete. Some studies suggested that neuroblastoma (NB) may be involved in this syndrome. Here, we describe the case of a 14-year-old female presenting with a multinodular goiter (MNG) and a collision tumor composed of NB and cystic nephroma (CN). She is a carrier of a deleterious germline mutation in exon 23 of DICER1 and harbored different somatic mutations in the CN and MNG. However, no second hit was found in the NB, questioning its status as a DICER1-related tumor.Entities:
Keywords: DICER1; cystic nephroma; multinodular goiter; mutation; neuroblastoma; syndrome
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Year: 2017 PMID: 28766837 DOI: 10.1002/pbc.26715
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167