Resende Cristina, Araújo Catarina, Duarte Maria da Luz, Vieira Ana Paula, Brito Celeste
Hospital de Braga, Braga, Portugal.
An Bras Dermatol. 2015 Mar-Apr;90(2):245-7. doi: 10.1590/abd1806-4841.20153228.
Kikuchi's disease is a benign, self-limiting disease, whose pathogenesis remains unknown. Patients most often present with cervical lymphadenopathy, sometimes associated with fever and leukopenia. It has been reported that up to 40% of patients with Kikuchi's disease have also cutaneous eruptions, but no specific skin changes have been described. Kikuchi's disease can be subclassified into three histologic subtypes: a proliferative type, a necrotizing type and a xantomathous type. Most patients with Kikuchi's disease require no specific treatment, because the disease regresses spontaneously, within a few weeks to months. We report a case of a 31-year-old woman with xanthomatous type of Kikuchi's disease, whose first manifestation was the onset of erythematous papules with central suppuration on her face and on her left hand.
菊池病是一种良性的自限性疾病,其发病机制尚不清楚。患者最常表现为颈部淋巴结病,有时伴有发热和白细胞减少。据报道,高达40%的菊池病患者也有皮肤疹,但尚未描述具体的皮肤变化。菊池病可分为三种组织学亚型:增殖型、坏死型和黄色瘤型。大多数菊池病患者不需要特殊治疗,因为该病会在几周至几个月内自行消退。我们报告一例31岁女性的黄色瘤型菊池病,其首发表现为面部和左手出现中央化脓的红斑丘疹。