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Gianotti-Crosti syndrome: case report of a pruritic acral exanthema in a child

机译:Gianotti-Crosti综合征:儿童瘙痒性肢端皮疹的病例报告

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摘要

Gianotti-Crosti syndrome (GCS) is a sporadic dermatosis affecting mainly children. It is characterized by multiple, confluent, monomorphic and pruritic pink to red-brown papules or papulovesicles, distributed symmetrically on the face, extensor surfaces of the extremities and buttocks, commonly sparing the trunk, palms and soles. This can be preceded by a viral infection, and may be accompanied by fever, hepatosplenomegaly, or lymphadenopathy. Personal and family history of atopy appears to be a risk factor in the subsequent development of GCS, thus frequently diagnosed as atopic dermatitis. We report a case of a 4-year-old boy from our institution with generalized, pruritic, papulovesicular rashes on the face and extremities for one month. He was diagnosed to have atopic dermatitis and treated as such, before presentation to our institution. As the signs and symptoms in GCS are similar to atopic dermatitis, we suggest that this diagnosis be considered when presented with a similar case.
机译:Gianotti-Crosti综合征(GCS)是一种偶发性皮肤病,主要影响儿童。它的特征是多个,融合的,单形的和瘙痒的粉红色至红棕色丘疹或丘疹,对称分布在四肢和臀部的面部,伸肌表面,通常不占用躯干,手掌和脚底。在此之前可以进行病毒感染,并可能伴有发烧,肝脾肿大或淋巴结病。特应性病的个人和家族史似乎是随后GCS发生的危险因素,因此经常被诊断为特应性皮炎。我们报告了一例来自我们机构的4岁男孩,其面部和四肢出现广泛性瘙痒性丘疹性皮疹一个月。他被诊断患有特应性皮炎,并在就诊之前接受了治疗。由于GCS的体征和症状与特应性皮炎相似,因此我们建议在出现类似病例时应考虑该诊断。

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