Congenital hepatic fibrosis and its mimics: a clinicopathologic study of 19 cases at a single institution

BACKGROUND: Congenital hepatic fibrosis (CHF) is a rare inherited form of ductal plate malformation associated with polycystic kidney disease. The diagnosis requires histopathologic confirmation, but can be challenging to distinguish from other undefined fibrocystic liver diseases. We aimed to descr...

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Detalles Bibliográficos
Autores principales: Chen, Irene Y., Whitney-Miller, Christa L., Liao, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406726/
https://www.ncbi.nlm.nih.gov/pubmed/34461951
http://dx.doi.org/10.1186/s13000-021-01142-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406726/
https://www.ncbi.nlm.nih.gov/pubmed/34461951
http://dx.doi.org/10.1186/s13000-021-01142-y

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