Symmetric drug-related intertriginous and flexural exanthema: Clinicopathologic study of 19 cases and review of literature.

baboon syndrome drug reaction with eosinophilia and systemic symptoms histopathology symmetric drug-related intertriginous and flexural exanthema toxic erythema of chemotherapy

Journal

Journal of cutaneous pathology
ISSN: 1600-0560
Titre abrégé: J Cutan Pathol
Pays: United States
ID NLM: 0425124

Informations de publication

Date de publication:
Dec 2021
Historique:
revised: 08 06 2021
received: 05 04 2021
accepted: 18 06 2021
pubmed: 24 6 2021
medline: 1 3 2022
entrez: 23 6 2021
Statut: ppublish

Résumé

Symmetric drug-related intertriginous and flexural exanthema (SDRIFE) is a cutaneous drug reaction characterized by gluteal/anogenital erythema and symmetric involvement of other intertriginous location(s) without systemic signs. Clinicopathologic characterization has been limited to case reports and small series. We describe 19 new cases and review the literature to better define the clinical and histopathologic spectrum of SDRIFE. Pathology archives were searched for "SDRIFE" and "baboon syndrome." Cases meeting clinical criteria were included. Clinical and histopathologic features were recorded. Previous reports of SDRIFE with histopathologic descriptions were reviewed. Nineteen new cases were included, over half triggered by antibiotics. Six new causative medications were identified. Median onset was 7 days. Typical lesions were erythematous plaques or papules with or without scale. The most common histopathologic finding was superficial perivascular lymphocytic infiltrate followed by dermal eosinophils, spongiosis, and orthokeratosis. Basal vacuolization and apoptotic keratinocytes were less common. Interstitial histiocytes were present in almost half of our cases. Other findings included atypical lymphocytes and "flame figure." Appreciation of the range of inciting medications and clinicopathologic features in SDRIFE will improve recognition of this condition. Although many histopathologic features overlap with other common dermatitides, biopsy may assist in excluding key clinical mimics.

Sections du résumé

BACKGROUND BACKGROUND
Symmetric drug-related intertriginous and flexural exanthema (SDRIFE) is a cutaneous drug reaction characterized by gluteal/anogenital erythema and symmetric involvement of other intertriginous location(s) without systemic signs. Clinicopathologic characterization has been limited to case reports and small series. We describe 19 new cases and review the literature to better define the clinical and histopathologic spectrum of SDRIFE.
METHODS METHODS
Pathology archives were searched for "SDRIFE" and "baboon syndrome." Cases meeting clinical criteria were included. Clinical and histopathologic features were recorded. Previous reports of SDRIFE with histopathologic descriptions were reviewed.
RESULTS RESULTS
Nineteen new cases were included, over half triggered by antibiotics. Six new causative medications were identified. Median onset was 7 days. Typical lesions were erythematous plaques or papules with or without scale. The most common histopathologic finding was superficial perivascular lymphocytic infiltrate followed by dermal eosinophils, spongiosis, and orthokeratosis. Basal vacuolization and apoptotic keratinocytes were less common. Interstitial histiocytes were present in almost half of our cases. Other findings included atypical lymphocytes and "flame figure."
CONCLUSIONS CONCLUSIONS
Appreciation of the range of inciting medications and clinicopathologic features in SDRIFE will improve recognition of this condition. Although many histopathologic features overlap with other common dermatitides, biopsy may assist in excluding key clinical mimics.

Identifiants

pubmed: 34159622
doi: 10.1111/cup.14090
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1471-1479

Informations de copyright

© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Andrew M Schuler (AM)

Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Emily H Smith (EH)

Department of Dermatology, University of Missouri, Columbia, Missouri, USA.

Kristine M Chaudet (KM)

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Scott C Bresler (SC)

Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Johann E Gudjonsson (JE)

Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Daniela Kroshinsky (D)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Rosalynn M Nazarian (RM)

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

May P Chan (MP)

Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.

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