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Symmetric drug-related intertriginous and flexural exanthema: Clinicopathologic study of 19 cases and review of literature.
Schuler, Andrew M; Smith, Emily H; Chaudet, Kristine M; Bresler, Scott C; Gudjonsson, Johann E; Kroshinsky, Daniela; Nazarian, Rosalynn M; Chan, May P.
Afiliação
  • Schuler AM; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Smith EH; Department of Dermatology, University of Missouri, Columbia, Missouri, USA.
  • Chaudet KM; Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Bresler SC; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Gudjonsson JE; Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Kroshinsky D; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Nazarian RM; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Chan MP; Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Cutan Pathol ; 48(12): 1471-1479, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34159622
ABSTRACT

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:

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:

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:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxidermias / Exantema / Intertrigo Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxidermias / Exantema / Intertrigo Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article