Case for diagnosis. patch granuloma annulare

dc.creatorGeraldo Magela Magalhães
dc.creatorCássio Ferreira Guimarães
dc.creatorMaysa Carla de Paula
dc.date.accessioned2023-10-30T20:29:31Z
dc.date.accessioned2025-09-09T01:33:47Z
dc.date.available2023-10-30T20:29:31Z
dc.date.issued2017
dc.format.mimetypepdf
dc.identifier.doi10.1590/abd1806-4841.20176729
dc.identifier.issn03650596
dc.identifier.urihttps://hdl.handle.net/1843/60268
dc.languagepor
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofAnais Brasileiros de Dermatologia
dc.rightsAcesso Aberto
dc.subjectDiagnosis, Differential
dc.subjectGranuloma Annulare
dc.subjectPathology
dc.subject.otherDiagnosis, Differential
dc.subject.otherGranuloma Annulare
dc.subject.otherPathology
dc.titleCase for diagnosis. patch granuloma annulare
dc.typeArtigo de periódico
local.citation.epage420
local.citation.issue3
local.citation.spage419
local.citation.volume92
local.description.resumoA 59-year-old woman reported a 20-day history of slightly scaly erythematous infiltrated patches on her palms and soles with a histopathological result which was consistent with interstitial-pattern granuloma annulare, clinically classified as patch granuloma annulare. This is a rare clinical variant of granuloma annulare, with an unknown incidence and characteristic clinical and histopathological features. The patient evolved with a complete remission of the lesions after biopsy and the use of high-potency topical corticosteroid.
local.publisher.countryBrasil
local.publisher.departmentMED - DEPARTAMENTO DE CLÍNICA MÉDICA
local.publisher.initialsUFMG
local.url.externahttps://doi.org/10.1590/abd1806-4841.20176729

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