| Literature DB >> 31067372 |
Maria Apellaniz-Ruiz1, Maria Segni1, Matthias Kettwig1, Sylvia Glüer1, Dylan Pelletier1, Van-Hung Nguyen1, Rabea Wagener1, Cristina López1, Karl Muchantef1, Dorothée Bouron-Dal Soglio1, Nelly Sabbaghian1, Mona K Wu1, Stefano Zannella1, Marc R Fabian1, Reiner Siebert1, Jan Menke1, John R Priest1, William D Foulkes1.
Abstract
Mesenchymal hamartoma of the liver (MHL) is a benign tumor affecting children that is characterized by a primitive myxoid stroma with cystically dilated bile ducts. Alterations involving chromosome 19q13 are a recurrent underlying cause of MHL; these alterations activate the chromosome 19 microRNA cluster (C19MC). Other cases remain unexplained. We describe two children with MHLs that harbored germline DICER1 pathogenic variants. Analysis of tumor tissue from one of the children revealed two DICER1 "hits." Mutations in DICER1 dysregulate microRNAs, mimicking the effect of the activation of C19MC. Our data suggest that MHL is a new phenotype of DICER1 syndrome. (Funded by the Canadian Institutes of Health Research and others.).Entities:
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Year: 2019 PMID: 31067372 DOI: 10.1056/NEJMoa1812169
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245