| Autor: |
Marcarini R; Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil., Araujo RN; Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil., Nóbrega MM; Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil., Medeiros KB; Universidade Federal do Espírito Santo (UFES) - Vitória (ES), Brazil., Gripp AC; Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil., Maceira JM; Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil.; Universidade Federal do Rio de Janeiro (UFRJ) - Rio de Janeiro (RJ), Brazil. |
| Jazyk: |
angličtina |
| Zdroj: |
Anais brasileiros de dermatologia [An Bras Dermatol] 2016 Sep-Oct; Vol. 91 (5 suppl 1), pp. 154-156. |
| DOI: |
10.1590/abd1806-4841.20164361 |
| Abstrakt: |
Histiocytoid Sweet's Syndrome is a rare inflammatory disease described in 2005 as a variant of the classical Sweet's Syndrome (SS). Histopathologically, the dermal inflammatory infiltrate is composed mainly of mononuclear cells that have a histiocytic appearance and represent immature myeloid cells. We describe a case of Histiocytoid Sweet's Syndrome in an 18-year-old man. Although this patient had clinical manifestations compatible with SS, the cutaneous lesions consisted of erythematous annular plaques, which are not typical for this entity and have not been described in histiocytic form so far. The histiocytic subtype was confirmed by histopathological analysis that showed positivity for myeloperoxidase in multiple cells with histiocytic appearance. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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