Cardoso Fernanda, Serafini Natália Battisti, Reis Brisa Dondoni, Nuñez Mónica Daniela Gauto, Nery José Augusto da Costa, Lupi Omar
General Polyclinic of Rio de Janeiro (Policlínica Geral do Rio de Janeiro - PGRJ), Rio de Janeiro, (RJ), Brazil.
An Bras Dermatol. 2013 Jan-Feb;88(1):105-8. doi: 10.1590/s0365-05962013000100015.
Generalized eruptive histiocytoma is considered an extremely rare subtype of non-Langerhans cells histiocytosis. In the literature, there are few reports of this disease that mainly affects adults. In this report, we present a case of generalized eruptive histiocytoma in an elderly patient who had presented symptoms for over two months. Multiple erythematous papules, asymptomatic and symmetrically distributed were observed on the trunk and limbs. Histological examination showed a dense mononuclear cell dermal infiltrate. In the immunohistochemical analysis, the cells were CD68 positive, but CD1a, S100 and CD34 negative. A diagnosis of generalized eruptive histiocytoma was established. The aim of our paper is to report a case of a very rare disease, whose subtype and affected age group are even more unusual.
泛发性发疹性组织细胞瘤被认为是非朗格汉斯细胞组织细胞增生症中一种极其罕见的亚型。在文献中,关于这种主要影响成年人的疾病的报道很少。在本报告中,我们呈现了一例老年泛发性发疹性组织细胞瘤病例,该患者出现症状已两个多月。在躯干和四肢观察到多个无症状且对称分布的红斑丘疹。组织学检查显示真皮有密集的单核细胞浸润。免疫组化分析中,细胞CD68阳性,但CD1a、S100和CD34阴性。确诊为泛发性发疹性组织细胞瘤。我们本文的目的是报告一例非常罕见的疾病,其亚型和受影响的年龄组更为不寻常。