Literature DB >> 24164717

Treatment of pruritus with Prometheus dialysis and absorption system in a patient with benign recurrent intrahepatic cholestasis.

Urszula Ołdakowska-Jedynak1, Irena Jankowska, Marek Hartleb, Milan Jirsa, Joanna Pawłowska, Piotr Czubkowski, Marek Krawczyk.   

Abstract

Benign recurrent intrahepatic cholestasis (BRIC) is an autosomal recessive liver disorder characterized by recurrent episodes of jaundice and itching. Episodes of cholestasis last variously from 1 week to several months, may start at any age and usually resolve spontaneously. No effective treatment has been found as yet. We report a case of genetically proven BRIC in a male patient who developed three episodes of pruritus and jaundice at the age of 14, 16 and 19 years. During the third episode, he did not respond to pharmacological medical therapy, and fractionated plasma separation and absorption (FPSA, Prometheus) was performed to manage intractable pruritus. The treatment immediately alleviated pruritus, lowered serum bilirubin concentration and induced sustained remission in the 5-year follow up. FPSA seems to be a safe and effective way of treatment for BRIC in patients with severe pruritus and prolonged jaundice.
© 2013 The Japan Society of Hepatology.

Entities:  

Keywords:  Prometheus; benign recurrent intrahepatic cholestasis; cholestasis; jaundice; pruritus

Year:  2013        PMID: 24164717     DOI: 10.1111/hepr.12262

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  4 in total

1.  Endoscopic nasobiliary drainage: an effective treatment option for benign recurrent intrahepatic cholestasis (BRIC).

Authors:  Ashok Choudhury; Anand V Kulkarni; Bishnupriya Sahoo; Chhagan Bihari
Journal:  BMJ Case Rep       Date:  2017-05-05

Review 2.  Hepatitis C virus-associated pruritus: Etiopathogenesis and therapeutic strategies.

Authors:  Youssef Alhmada; Denis Selimovic; Fadi Murad; Sarah-Lilly Hassan; Youssef Haikel; Mossaad Megahed; Matthias Hannig; Mohamed Hassan
Journal:  World J Gastroenterol       Date:  2017-02-07       Impact factor: 5.742

3.  Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.

Authors:  Ayumu Mizutani; Yusuke Sabu; Sotaro Naoi; Shogo Ito; Satoshi Nakano; Kei Minowa; Tatsuki Mizuochi; Koichi Ito; Daiki Abukawa; Shunsaku Kaji; Mika Sasaki; Koji Muroya; Yoshihiro Azuma; Satoshi Watanabe; Yuki Oya; Yukihiro Inomata; Akinari Fukuda; Mureo Kasahara; Ayano Inui; Hajime Takikawa; Hiroyuki Kusuhara; Kazuhiko Bessho; Mitsuyoshi Suzuki; Takao Togawa; Hisamitsu Hayashi
Journal:  Hepatol Commun       Date:  2020-09-26

Review 4.  New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications.

Authors:  Eva Sticova; Milan Jirsa; Joanna Pawłowska
Journal:  Can J Gastroenterol Hepatol       Date:  2018-07-26
  4 in total

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