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Rapid response of IgA pemphigus of subcorneal pustular dermatosis type to treatment with isotretinoin

Claus Gruss*, Detlef Zillikens, Takashi Hashimoto, Masayuki Amagai, Maximilian Kroiss, Thomas Vogt, Michael Landthaler, Wilhelm Stolz

*Corresponding author for this work

Abstract

Diagnosing IgA pemphigus and distinguishing between its 2 subtypes, intraepidermal neutrophilic IgA dermatosis type and subcorneal pustular dermatosis type, is important because treatment of IgA pemphigus has to be different from treatment of other blistering autoimmune dermatoses. We present a patient with subcorneal pustular dermatosis type of IgA pemphigus who rapidly responded to systemic treatment with isotretinoin. Specific diagnosis was established by detecting IgA serum activity to desmocollin 1 by indirect immunofluorescence microscopy on unfixed COS7 cells transfected with desmocollin 1. No IgA or IgG serum reactivity was found to recombinant forms of desmogleins 1 and 3 by an antigen-specific enzyme-linked immunosorbent assay. The disease was not effectively controlled by conventional therapeutic regimens. Systemic treatment with isotretinoin 20 mg daily led to complete clearance of skin lesions within 3 weeks. Assaying IgA serum reactivity to desmocollin 1, desmoglein 1, and desmoglein 3 as a valuable method for establishing the diagnosis and differentiating the 2 subtypes of IgA pemphigus. Isotretinoin was an effective drug in the treatment of subcorneal pustular dermatosis type of IgA pemphigus in this patient.

Original languageEnglish
JournalJournal of the American Academy of Dermatology
Volume43
Issue number5 SPEC. SUPPL.
Pages (from-to)923-926
Number of pages4
ISSN0190-9622
DOIs
Publication statusPublished - 2000

Funding

This supplement is made possible through an educational grant from Ortho Dermatological to the American Academy of Dermatology.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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