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Hepar Lobatum carcinomatosum: A rare cause of portal hypertension

Hepar lobatum carcinomatosum is a rare form of major hepatic dysmorphia secondary to metastatic breast cancer. This condition seems to be related to the obstruction of portal vessels by tumor cells responsible of possible secondary portal hypertension without underlying cirrhosis.

Detalles Bibliográficos
Autores principales: Mathis, Guillaume, Felli, Emanuele, Mutter, Didier, Pessaux, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562830/
https://www.ncbi.nlm.nih.gov/pubmed/33088561
http://dx.doi.org/10.1002/ccr3.3052
Descripción
Sumario:Hepar lobatum carcinomatosum is a rare form of major hepatic dysmorphia secondary to metastatic breast cancer. This condition seems to be related to the obstruction of portal vessels by tumor cells responsible of possible secondary portal hypertension without underlying cirrhosis.