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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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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