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Histology of portal vascular changes associated with idiopathic non‐cirrhotic portal hypertension: nomenclature and definition.

Authors :
Guido, Maria
Alves, Venancio A F
Balabaud, Charles
Bathal, Prithi S
Bioulac‐Sage, Paulette
Colombari, Romano
Crawford, James M
Dhillon, Amar P
Ferrell, Linda D
Gill, Ryan M
Hytiroglou, Prodromos
Nakanuma, Yasuni
Paradis, Valerie
Quaglia, Alberto
Rautou, Pierre E
Theise, Neil D
Thung, Swan
Tsui, Wilson M S
Sempoux, Christine
Snover, Dale
Source :
Histopathology; Jan2019, Vol. 74 Issue 2, p219-226, 8p, 4 Color Photographs, 1 Chart
Publication Year :
2019

Abstract

Idiopathic non‐cirrhotic portal hypertension (INCPH) is a rare vascular liver disease that has attracted new interest in recent years. It is characterised by clinical signs of portal hypertension in the absence of cirrhosis or severe fibrosis and any known cause of portal hypertension. As much uncertainty exists about INCPH pathophysiology, and no definite diagnostic tests are available, liver biopsy is an essential tool for achieving a definite diagnosis. Unfortunately, the histological diagnosis of INCPH is not always straightforward, as the characteristic lesions are unevenly distributed, vary greatly in their severity, are often very subtle, and are not all necessarily present in a single case. Furthermore, specifically for the characteristic portal vessel changes observed in INCPH, the terminology and definition are ambiguous, which adds complexity to the already complex clinicopathological scenario. An international study group of liver pathologists and hepatologists pursued a consensus on nomenclature for the portal vascular lesions of INCPH. Such standardisation may assist pathologists in the recognition of such lesions, and will possibly facilitate further advancement in this field. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03090167
Volume :
74
Issue :
2
Database :
Complementary Index
Journal :
Histopathology
Publication Type :
Academic Journal
Accession number :
133627151
Full Text :
https://doi.org/10.1111/his.13738