A case of concomitant subcorneal pustular dermatosis and erythema nodosum leprosum in borderline lepromatous leprosy-relapses

H. Gunawan, Nina Roslina, O. Suwarsa
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引用次数: 1

Abstract

Subcorneal pustular dermatosis (SPD) is a rare, chronic, and recurrent pustular eruption characterized histopathologically by subcorneal pustules that contain neutrophils. SPD has been clearly reported conjunction with other diseases. Leprosy reactions are acute inflammatory process that immunologically driven on the chronic course of leprosy. Erythema nodosum leprosum (ENL) is a type II of leprosy reaction putatively can initiate SPD lesions. We report one case of concomitant SPD and ENL in borderline lepromatous leprosy-relapses. A 41-year-old man with the history of using multidrug therapy-multibacillary for leprosy presented with painful erythematous nodules on the trunk and extremities, accompanied by pustules on erythematous base on the face, arms, buttocks, and legs. There were thickening of both ulnar nerves with gloves and stocking hypesthesia. The bacterial index was 3+ and morphological index was 20\%. Histopathological examination on the pustule revealed subcorneal pustules with exocytosis of neutrophils which supported the diagnosis of SPD. A possible immunologic mechanism has been suggested in the induction of the occurence both SPD and ENL.
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边缘型麻风复发并发角膜下脓疱性皮肤病和结节性红斑1例
摘要角膜下脓疱性皮肤病(SPD)是一种罕见的、慢性的、反复发作的脓疱性皮肤病,其组织病理学特征为含有中性粒细胞的角膜下脓疱。SPD已被明确报道与其他疾病合并。麻风反应是免疫驱动的麻风慢性病程的急性炎症过程。麻风结节性红斑(ENL)是一种II型麻风反应,可以引发SPD病变。我们报告一例交界型麻风复发伴发SPD和ENL。1例41岁男性,有麻风病多药多菌治疗史,其躯干和四肢出现疼痛的红斑结节,并伴有面部、手臂、臀部和腿部红斑基部的脓疱。戴手套和长统袜均有尺神经增厚。细菌指数为3+,形态指数为20%。组织病理学检查发现角膜下脓疱伴中性粒细胞分泌,支持SPD的诊断。SPD和ENL的发生可能存在一种免疫机制。
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