Open AccessA Rare Case Report on Benign Recurrent Intrahepatic Cholestasis
Author(s) -
Kaisar Niaz,
Dewan Saifuddin Ahmed,
Syeda Nur E Jannat,
Quazi Abdullah Al Masum,
Muhammad Sayedul Arifin,
Bikas Kumar Paul,
Akm Jubaere,
Shakhawat Hossain,
Mukesh Prasad Sah,
Rabiul Islam,
Abdul Mumit Sarkar,
Farid Ahmed Titu,
S. M. Yasir Arafat,
Pinaki Paul,
Syed Shariful Islam,
Mizanur Rahman,
Azam Jahanger,
Gobinda Gain,
Aqm Mobin,
Naymul Hassan,
Birendra Nath Saha,
Sayeda Tasnim Haq
Publication year - 2015
Publication title -
faridpur medical college journal
Language(s) - English
Resource type - Journals
eISSN - 2312-9093
pISSN - 2079-3553
DOI - 10.3329/fmcj.v9i2.25688
Subject(s) - medicine , cholestasis , jaundice , obstructive jaundice , progressive familial intrahepatic cholestasis , rare disease , disease , symptomatic treatment , gastroenterology , pediatrics , transplantation , liver transplantation
Benign recurrent intrahepatic cholestasis is an inherited and occasionally sporadic disease presents as recurrent episodes of obstructive jaundice without any obstruction in billiary channel with intervening symptom free periods. Here we are presenting a case of 20-year-old male with a recurrent jaundice and pruritus who later diagnose as BRIC.Faridpur Med. Coll. J. 2014;9(2): 108-110