New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: does it fit with the syndrome?

BACKGROUND: Hepatocyte nuclear factor 1B (HNF1B) is a member of the homeodomain-containing family of transcription factors located on 17q12. HNF1B deficiency is associated with a clinical syndrome (kidney and urogenital malformations, maturity-onset diabetes of the young, exocrine pancreatic insuffi...

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Detalles Bibliográficos
Autores principales: Pinon, Michele, Gambella, Alessandro, Giugliano, Laura, Chiadò, Cristina, Kalantari, Silvia, Bracciamà, Valeria, Deaglio, Silvia, Tinti, Davide, Peruzzi, Licia, Cotti, Roberta, Catalano, Silvia, Cadamuro, Massimiliano, Fabris, Luca, Calvo, Pier Luigi, Romagnoli, Renato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Hepatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806080/
https://www.ncbi.nlm.nih.gov/pubmed/36572455
http://dx.doi.org/10.1136/bmjgast-2022-001013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806080/
https://www.ncbi.nlm.nih.gov/pubmed/36572455
http://dx.doi.org/10.1136/bmjgast-2022-001013

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