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Portopulmonary hypertension in a case of non-cirrhotic portal fibrosis.
Indian J Pathol Microbiol ; 2007 Oct; 50(4): 828-30
Article in English | IMSEAR | ID: sea-74815
ABSTRACT
Portopulmonary hypertension (PPHT) is the unusual association of portal hypertension (HT) with pulmonary HT. We report a case of noncirrhotic portal fibrosis (NCPF) leading to PPHT which is exceedingly rare with only very few cases reported in the literature. This is an autopsy report of a 30 years old man, a known case of portal HT who died suddenly due to a syncopal attack. Autopsy revealed massive pulmonary thromobembolism with pulmonary HT. Liver showed changes of NCPF. The rarity of NCPF causing PPHT prompted this case report.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pulmonary Embolism / Autopsy / Syncope / Humans / Male / Fatal Outcome / Adult / Hypertension, Portal / Hypertension, Pulmonary / Liver Cirrhosis Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pulmonary Embolism / Autopsy / Syncope / Humans / Male / Fatal Outcome / Adult / Hypertension, Portal / Hypertension, Pulmonary / Liver Cirrhosis Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article