| Literature DB >> 29883781 |
Markus Eckstein1, Abbas Agaimy2, Joachim Woenckhaus3, Alexander Winter4, Iris Bittmann5, Joerg Janzen6, Simone Bertz2, Florian Haller2, Arndt Hartmann2.
Abstract
Fibroepithelial polyps of the urinary tract are rare lesions. They occur mainly in the upper urinary tract of children. A high disease prevalence has been reported in families with pleuropulmonary blastoma. Here we present a case of a 46-year-old woman who presented with a giant botryoid fibroepithelial polyp of the urinary bladder. Histologically, the lesion showed prominent botryoid features with an embryonal rhabdomyosarcoma-like cambium layer lacking nuclear or cellular atypia. Immunohistochemical analysis ruled out rhabdomyoblastic differentiation. Next-generation sequencing was performed on the polyp tissue and revealed two pathogenic mutations in the DICER1 ribonuclease III (DICER1) gene (c.[5439G>T]; p.[Glu1813Asp] and c.[1525C>T]; p.[Arg509*]). Truncating DICER1 mutations, accompanied by characteristic "hotspot" mutations affecting the RNase IIIB domain of DICER1 are typically seen in DICER1-related lesions. Our findings indicate a role of DICER1 mutations in the pathogenesis of fibroepithelial polyps of the urinary tract.Entities:
Keywords: DICER1; DICER1 syndrome; Embryonal rhabdomyosarcoma; Fibroepithelial polyps; Pleuropulmonary blastoma
Mesh:
Substances:
Year: 2018 PMID: 29883781 DOI: 10.1016/j.humpath.2018.05.015
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466