Idiopathic portal hypertension complicating systemic sclerosis: a case report

<p>Abstract</p> <p>Background</p> <p>Patients with systemic sclerosis may develop mild abnormalities of liver function tests. More serious hepatic involvement has been well documented but is rare. Idiopathic portal hypertension had been reported only in a few female pat...

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Main Authors: Henry James, Kelly Clive, Leontiadis Grigoris I, Moschos John, Kadis Savvas
Format: Article
Language:English
Published: BMC 2005-05-01
Series:BMC Gastroenterology
Online Access:http://www.biomedcentral.com/1471-230X/5/16
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spelling doaj-86bbaf7527064f02b3c190b61099bdb22020-11-25T03:42:09ZengBMCBMC Gastroenterology1471-230X2005-05-01511610.1186/1471-230X-5-16Idiopathic portal hypertension complicating systemic sclerosis: a case reportHenry JamesKelly CliveLeontiadis Grigoris IMoschos JohnKadis Savvas<p>Abstract</p> <p>Background</p> <p>Patients with systemic sclerosis may develop mild abnormalities of liver function tests. More serious hepatic involvement has been well documented but is rare. Idiopathic portal hypertension had been reported only in a few female patients with systemic sclerosis.</p> <p>Case presentation</p> <p>An 82-year-old man with known systemic sclerosis presented with melaena. Urgent gastroscopy revealed oesophageal varices, which re-started bleeding during the procedure and were treated ensocopically, with Sengstaken tube and glypressin. Liver function tests and coagulation were normal. Non-invasive liver screen (including hepatitis viral serology and autoantibodies) was negative. Ultrasound scan of the abdomen revealed a small liver with coarse texture and no focal lesion. Hepato-portal flow was demonstrated in the portal vein. The spleen was enlarged. A moderate amount of free peritoneal fluid was present. A CT scan confirmed the absence of portal vein thrombosis. One month following discharge the patient had a liver biopsy. Histological examination showed essentially normal liver tissue; there was no evidence of any excess inflammation and no features to suggest cirrhosis or drug-induced liver disease. Taking into account the above evaluation we concluded that the patient had idiopathic portal hypertension.</p> <p>Conclusion</p> <p>Both male and female patients with systemic sclerosis may – rarely – develop idiopathic portal hypertension.</p> http://www.biomedcentral.com/1471-230X/5/16
collection DOAJ
language English
format Article
sources DOAJ
author Henry James
Kelly Clive
Leontiadis Grigoris I
Moschos John
Kadis Savvas
spellingShingle Henry James
Kelly Clive
Leontiadis Grigoris I
Moschos John
Kadis Savvas
Idiopathic portal hypertension complicating systemic sclerosis: a case report
BMC Gastroenterology
author_facet Henry James
Kelly Clive
Leontiadis Grigoris I
Moschos John
Kadis Savvas
author_sort Henry James
title Idiopathic portal hypertension complicating systemic sclerosis: a case report
title_short Idiopathic portal hypertension complicating systemic sclerosis: a case report
title_full Idiopathic portal hypertension complicating systemic sclerosis: a case report
title_fullStr Idiopathic portal hypertension complicating systemic sclerosis: a case report
title_full_unstemmed Idiopathic portal hypertension complicating systemic sclerosis: a case report
title_sort idiopathic portal hypertension complicating systemic sclerosis: a case report
publisher BMC
series BMC Gastroenterology
issn 1471-230X
publishDate 2005-05-01
description <p>Abstract</p> <p>Background</p> <p>Patients with systemic sclerosis may develop mild abnormalities of liver function tests. More serious hepatic involvement has been well documented but is rare. Idiopathic portal hypertension had been reported only in a few female patients with systemic sclerosis.</p> <p>Case presentation</p> <p>An 82-year-old man with known systemic sclerosis presented with melaena. Urgent gastroscopy revealed oesophageal varices, which re-started bleeding during the procedure and were treated ensocopically, with Sengstaken tube and glypressin. Liver function tests and coagulation were normal. Non-invasive liver screen (including hepatitis viral serology and autoantibodies) was negative. Ultrasound scan of the abdomen revealed a small liver with coarse texture and no focal lesion. Hepato-portal flow was demonstrated in the portal vein. The spleen was enlarged. A moderate amount of free peritoneal fluid was present. A CT scan confirmed the absence of portal vein thrombosis. One month following discharge the patient had a liver biopsy. Histological examination showed essentially normal liver tissue; there was no evidence of any excess inflammation and no features to suggest cirrhosis or drug-induced liver disease. Taking into account the above evaluation we concluded that the patient had idiopathic portal hypertension.</p> <p>Conclusion</p> <p>Both male and female patients with systemic sclerosis may – rarely – develop idiopathic portal hypertension.</p>
url http://www.biomedcentral.com/1471-230X/5/16
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AT leontiadisgrigorisi idiopathicportalhypertensioncomplicatingsystemicsclerosisacasereport
AT moschosjohn idiopathicportalhypertensioncomplicatingsystemicsclerosisacasereport
AT kadissavvas idiopathicportalhypertensioncomplicatingsystemicsclerosisacasereport
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