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.
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Online Access: | https://doi.org/10.1002/ccr3.3052 |
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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 |
_version_ |
1724545128413003776 |