| Literature DB >> 25356068 |
Kris Ann Schultz1, Jiandong Yang2, Leslie Doros3, Gretchen M Williams1, Anne Harris1, Douglas R Stewart4, Yoav Messinger1, Amanda Field5, Louis P Dehner6, D Ashley Hill7.
Abstract
Germline mutations in DICER1 are associated with increased risk for a wide variety of neoplastic conditions, including pleuropulmonary blastoma (PPB), cystic nephroma, nasal chondromesenchymal hamartoma, ovarian Sertoli-Leydig cell tumors, botryoid embryonal rhabdomyosarcoma of the uterine cervix, ciliary body medulloepithelioma, pineoblastoma, pituitary blastoma and nodular thyroid hyperplasia or thyroid carcinoma. These tumors may be seen in isolation or in constellation with other characteristic tumor types in individuals or family members. Here we describe the medical history of a child with a heterozygous, loss of function germline DICER1 mutation and multiple tumors associated with the syndrome.. Although germline mutations in DICER1 are rare, tumors of these types will be seen by practicing pathologists and should prompt consideration of an underlying DICER1 mutation.Entities:
Keywords: DICER1; Sertoli-Leydig; nasal chondromesenchymal hamartoma; pleuropulmonary blastoma; thyroid carcinoma
Year: 2014 PMID: 25356068 PMCID: PMC4209484 DOI: 10.1097/PCR.0000000000000027
Source DB: PubMed Journal: Pathol Case Rev ISSN: 1082-9784