Progesterone Hypersensitivity: The Utility of a Janus Kinase Inhibitor for Recurrent Erythema Multiforme

Andrew Claffey, Melanie Evans, Melissa Mauskar, Jason Jarin

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Progestogen hypersensitivity (PH) is a rare phenomenon reported in women with an immunologic response to rising progesterone levels in the luteal phase. This disease's rarity and clinical spectrum make it challenging to diagnose. Case: In this case report, we will discuss a 14-year-old female with monthly oral mucositis and palmar lesions consistent with erythema multiforme. Over 2 years, she underwent an extensive multidisciplinary workup and was trialed on many different medical therapies. Summary and Conclusion: The prevalence of PH has grown in the literature over the past decade. Due to progesterone's role in many biochemical pathways, the pathophysiology is complex. Although many modalities are efficacious for treating PH's cyclical eruptions, we propose treatment with a Janus kinase inhibitor when hormonal management alone is insufficient.

Original languageEnglish (US)
Pages (from-to)378-380
Number of pages3
JournalJournal of pediatric and adolescent gynecology
Volume37
Issue number3
DOIs
StateAccepted/In press - 2024

Keywords

  • Autoimmune progesterone dermatitis
  • Erythema multiforme
  • JAK inhibitor
  • Progesterone hypersensitivity

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology

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