Literature DB >> 28885418

Autoimmune Progesterone Dermatitis Presenting as Stevens-Johnson Syndrome.

Sara M Drayer1, Larry R Laufer, Maureen E Farrell.   

Abstract

BACKGROUND: Autoimmune progesterone dermatitis is an uncommon disease presenting with cyclical skin eruptions corresponding with the menstrual cycle luteal phase. Because symptoms are precipitated by rising progesterone levels, treatment relies on hormone suppression. CASE: A 22-year-old nulligravid woman presented with symptoms mistaken for Stevens-Johnson syndrome. A cyclic recurrence of her symptoms was noted, and the diagnosis of autoimmune progesterone dermatitis was made by an intradermal progesterone challenge. After 48 months, she remained refractory to medical management and definitive surgical treatment with bilateral oophorectomy was performed.
CONCLUSION: Autoimmune progesterone dermatitis is a challenging diagnosis owing to its rarity and variety of clinical presentations. Treatment centers on suppression of endogenous progesterone and avoidance of exogenous triggers. When these modalities fail, surgical management must be undertaken.

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Year:  2017        PMID: 28885418     DOI: 10.1097/AOG.0000000000002256

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  2 in total

Review 1.  Presentation and natural history of progestogen hypersensitivity.

Authors:  Dinah Foer; Kathleen M Buchheit
Journal:  Ann Allergy Asthma Immunol       Date:  2018-10-26       Impact factor: 6.347

2.  Autoimmune progesterone dermatitis following vaginal progesterone exposure in pregnancy.

Authors:  Tomi T Kanninen; Michael L Moretti; Nisha A Lakhi
Journal:  Obstet Med       Date:  2018-05-04
  2 in total

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