Hepar Lobatum carcinomatosum: A rare cause of portal hypertension

Abstract 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.

Bibliographic Details
Main Authors:	Guillaume Mathis, Emanuele Felli, Didier Mutter, Patrick Pessaux
Format:	Article
Language:	English
Published:	Wiley 2020-10-01
Series:	Clinical Case Reports
Subjects:	gastroenterology hepatology liver disease oncology portal hypertension
Online Access:	https://doi.org/10.1002/ccr3.3052

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spelling	doaj-9a2143484b904f3e96f9e3b5f387c3b92020-11-25T03:37:35ZengWileyClinical Case Reports2050-09042020-10-018102082208310.1002/ccr3.3052Hepar Lobatum carcinomatosum: A rare cause of portal hypertensionGuillaume Mathis0Emanuele Felli1Didier Mutter2Patrick Pessaux3Hôpitaux Universitaires de Strasbourg Chirurgie Digestive et Endocrinienne ‐ Nouvel Hôpital Civil Strasbourg FranceHôpitaux Universitaires de Strasbourg Chirurgie Digestive et Endocrinienne ‐ Nouvel Hôpital Civil Strasbourg FranceHôpitaux Universitaires de Strasbourg Chirurgie Digestive et Endocrinienne ‐ Nouvel Hôpital Civil Strasbourg FranceHôpitaux Universitaires de Strasbourg Chirurgie Digestive et Endocrinienne ‐ Nouvel Hôpital Civil Strasbourg FranceAbstract 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.https://doi.org/10.1002/ccr3.3052gastroenterologyhepatologyliver diseaseoncologyportal hypertension
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Guillaume Mathis Emanuele Felli Didier Mutter Patrick Pessaux
spellingShingle	Guillaume Mathis Emanuele Felli Didier Mutter Patrick Pessaux Hepar Lobatum carcinomatosum: A rare cause of portal hypertension Clinical Case Reports gastroenterology hepatology liver disease oncology portal hypertension
author_facet	Guillaume Mathis Emanuele Felli Didier Mutter Patrick Pessaux
author_sort	Guillaume Mathis
title	Hepar Lobatum carcinomatosum: A rare cause of portal hypertension
title_short	Hepar Lobatum carcinomatosum: A rare cause of portal hypertension
title_full	Hepar Lobatum carcinomatosum: A rare cause of portal hypertension
title_fullStr	Hepar Lobatum carcinomatosum: A rare cause of portal hypertension
title_full_unstemmed	Hepar Lobatum carcinomatosum: A rare cause of portal hypertension
title_sort	hepar lobatum carcinomatosum: a rare cause of portal hypertension
publisher	Wiley
series	Clinical Case Reports
issn	2050-0904
publishDate	2020-10-01
description	Abstract 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.
topic	gastroenterology hepatology liver disease oncology portal hypertension
url	https://doi.org/10.1002/ccr3.3052
work_keys_str_mv	AT guillaumemathis heparlobatumcarcinomatosumararecauseofportalhypertension AT emanuelefelli heparlobatumcarcinomatosumararecauseofportalhypertension AT didiermutter heparlobatumcarcinomatosumararecauseofportalhypertension AT patrickpessaux heparlobatumcarcinomatosumararecauseofportalhypertension
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Hepar Lobatum carcinomatosum: A rare cause of portal hypertension

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