BMC oral health · 2025
Systemic lupus erythematosus presenting as atypical erythema multiforme-like lesions: a diagnostic challenge.
СтатьяКлинический случайНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Hu Xiaojing, Liu Fen, Zong Juanjuan
Аннотация
OBJECTIVES: Systemic Lupus Erythematosus (SLE) can cause oral mucosal lesions, it is a severe autoimmune disease, manifesting as variable kinds of oral lesions. Occasionally, these clinical manifestations maybe be misdiagnosed as other diseases. The aim of the present article is to report a rare case of SLE oral mucosa lesions masquerading as an Erythema multiforme (EM) oral lesions in a young man.
CASE PRESENTATION: A 34-year-old man with acutely oral lesions for about 10 days, presenting as diffusely oral mucosal hyperemia, erosions and ulcerations. The history, the clinical manifestations of the oral mucosal lesions, palms erythematous plaques and painless target lesions, lower limbs painless erythema and laboratory tests results were comprehensively considered. Finally the case was diagnosed as SLE.
CONCLUSIONS: The report of EM-like oral mucosal lesion of SLE is an extremely rare finding. In the diagnosis of SLE or EM, it is important to consider the history, clinical information and hematological examination. Sometimes histopathology and immunofluorescence are necessary.
CASE PRESENTATION: A 34-year-old man with acutely oral lesions for about 10 days, presenting as diffusely oral mucosal hyperemia, erosions and ulcerations. The history, the clinical manifestations of the oral mucosal lesions, palms erythematous plaques and painless target lesions, lower limbs painless erythema and laboratory tests results were comprehensively considered. Finally the case was diagnosed as SLE.
CONCLUSIONS: The report of EM-like oral mucosal lesion of SLE is an extremely rare finding. In the diagnosis of SLE or EM, it is important to consider the history, clinical information and hematological examination. Sometimes histopathology and immunofluorescence are necessary.