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Annular neutrophilic dermatoses.
Koska, Mahmut Can; Karadag, Ayse Serap; Durdu, Murat.
Afiliação
  • Koska MC; Dermatology and Venereology Clinic, Artvin State Hospital, Artvin, Turkey. Electronic address: cankoska90@gmail.com.
  • Karadag AS; Department of Dermatology, Istanbul Arel University Medical Faculty, Istanbul, Turkey.
  • Durdu M; Department of Dermatology, Baskent University Faculty of Medicine, Adana Dr. Turgut Noyan Application and Research Center, Adana, Turkey.
Clin Dermatol ; 41(3): 340-354, 2023.
Article em En | MEDLINE | ID: mdl-37423267
ABSTRACT
Neutrophilic dermatoses (NDs) constitute a group of diseases characterized by sterile neutrophilic infiltrations. Many NDs usually present with infiltrated erythematous plaques, nodules, urticarial plaques, or pustules. Lesions may show variability, and atypical presentations may develop among NDs. Annular lesions have been reported in many NDs and may lead to diagnostic problems. Clinical features and histopathologic findings such as localization of the neutrophilic infiltrate, existence of other cell types, and absence of true vasculitis may be helpful to distinguish NDs. Some of these NDs are associated with infections, inflammatory diseases, and malignancies. In most NDs, systemic steroids and dapsone are very effective and usually first choices. Colchicine, antimicrobials such as doxycycline, tetracycline, and sulfapyridine, and other immunosuppressants such as cyclosporin, methotrexate, and mycophenolate mofetil have been used successfully in treating many NDs. Tumor necrosis factor α inhibitors have also been used successfully in treating many NDs. Janus kinase inhibitors are effective in CANDLE (chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature) syndrome, anakinra in neutrophilic urticarial dermatosis, and intravenous immunoglobulin in resistant pyoderma gangrenosum. We discuss the diagnosis and management of NDs that may present with annular lesions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article