Pedreira Renata Leite, Leal Juliana Martins, Silvestre Keline Jácome, Lisboa Alice Paixão, Gripp Alexandre Carlos
Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil.
An Bras Dermatol. 2016 Sep-Oct;91(5 suppl 1):163-165. doi: 10.1590/abd1806-4841.20164410.
Gianotti-Crosti syndrome is a rare disease characterized by acral papular eruption with symmetrical distribution. It is a benign and self-limited disease; the symptoms disappear after two to eight weeks, without recurrences or scars. Skin lesions are usually asymptomatic. Prodrome might occur, suggesting upper respiratory infection, or constitutional symptoms. Diagnosis is eminently clinical, and this disease is associated with viral infections. Due to its rarity and low occurrence in adolescents and adults, we report a case of Gianotti-Crosti syndrome of a teenager.
詹诺蒂-克罗西综合征是一种罕见疾病,其特征为肢端丘疹性皮疹,呈对称分布。它是一种良性自限性疾病;症状在两到八周后消失,不会复发或留下疤痕。皮肤病变通常无症状。可能会出现前驱症状,提示上呼吸道感染或全身症状。诊断主要依靠临床,且该疾病与病毒感染有关。由于其在青少年和成年人中罕见且发病率低,我们报告一例青少年詹诺蒂-克罗西综合征病例。