首页 | 本学科首页   官方微博 | 高级检索  
检索        


A case of autoimmune progesterone dermatitis diagnosed by progesterone pessary
Authors:Le Katie  Wood Glenda
Institution:Skin and Cancer Foundation, Sydney, New South Wales, Australia. katie.le@unsw.edu.au
Abstract:Autoimmune progesterone dermatitis is a rare, cyclical eruption that occurs in the luteal phase of the menstrual cycle and during pregnancy. Many manifestations have been reported including cyclical eczema, urticaria, erythema multiforme, stomatitis and even anaphylaxis. The condition spontaneously resolves after menopause. As histopathology is non-specific, the diagnosis rests on history with precipitation of the eruption by a progesterone challenge, usually by the intradermal, intramuscular or oral route. We present the case of a 34-year-old woman with a premenstrual papular and eczematous eruption that was exacerbated after pregnancy. Biopsy showed subacute spongiotic dermatitis. To confirm the diagnosis, we used an intravaginal progesterone pessary as a provocation challenge. There was recurrence of the rash 12 h after insertion of the pessary with spontaneous resolution thereafter. We propose that use of a progesterone pessary is an effective tool in the diagnosis of autoimmune progesterone dermatitis.
Keywords:autoimmune  danazol  dermatitis  luteinising hormone releasing hormone analogue  oophorectomy  ovulation  pessary  progesterone  tamoxifen
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号