Autoimmune progesterone dermatitis as a clue to refractory jaundice in a young woman
- 1 January 2021
- journal article
- letter
- Published by Wiley in Clinical and Experimental Dermatology
- Vol. 46 (1), 163-164
- https://doi.org/10.1111/ced.14332
Abstract
A lady in her 20s presented to the emergency department with profound icterus which had not resolved with standard hepato‐protective measures (ursodeoxycholic acid, cholestyramine, N‐acetyl cysteine). She had nausea, malaise and intense pruritus all over the body. Drug history revealed the intake of progesterone (norethisterone acetate, 5mg/day) for menorrhagia one week prior to the development of the icterus. Blood investigations revealed raised total bilirubin=24.4mg/dL, (direct =23.9mg/dL) and serum alkaline phosphatase=206 IU/L, (44‐147) with normal liver enzyme levels.This publication has 6 references indexed in Scilit:
- Autoimmune progesterone dermatitis: Update and insightsAutoimmunity Reviews, 2016
- Role of sex hormones in the modulation of cholangiocyte functionWorld Journal of Gastrointestinal Pathophysiology, 2010
- Intrahepatic cholestasis of pregnancy: A randomized controlled trial comparing dexamethasone and ursodeoxycholic acidHepatology, 2005
- Norethisterone-induced cholestasisQJM: An International Journal of Medicine, 2005
- Expression of progesterone receptor in human keratinocytesJournal of Korean Medical Science, 2000
- Autoimmune Progesterone DermatitisArchives of Dermatology, 1977