Idiopathic Noncirrhotic Portal Hypertension: An Appraisal.

Autor: Lee H; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA., Rehman AU; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA., Fiel MI; Department of Pathology, The Mount Sinai Medical Center, New York, NY, USA.
Jazyk: angličtina
Zdroj: Journal of pathology and translational medicine [J Pathol Transl Med] 2016 Jan; Vol. 50 (1), pp. 17-25. Date of Electronic Publication: 2015 Nov 11.
DOI: 10.4132/jptm.2015.09.23
Abstrakt: Idiopathic noncirrhotic portal hypertension is a poorly defined clinical condition of unknown etiology. Patients present with signs and symptoms of portal hypertension without evidence of cirrhosis. The disease course appears to be indolent and benign with an overall better outcome than cirrhosis, as long as the complications of portal hypertension are properly managed. This condition has been recognized in different parts of the world in diverse ethnic groups with variable risk factors, resulting in numerous terminologies and lack of standardized diagnostic criteria. Therefore, although the diagnosis of idiopathic noncirrhotic portal hypertension requires clinical exclusion of other conditions that can cause portal hypertension and histopathologic confirmation, this entity is under-recognized clinically as well as pathologically. Recent studies have demonstrated that variable histopathologic entities with different terms likely represent a histologic spectrum of a single entity of which obliterative portal venopathy might be an underlying pathogenesis. This perception calls for standardization of the nomenclature and formulation of widely accepted diagnostic criteria, which will facilitate easier recognition of this disorder and will highlight awareness of this entity.
Databáze: MEDLINE