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系统性红斑狼疮患者的丘疹结节性粘蛋白病 1 例。

A Case of Papulonodular Mucinosis in a Patient With Systemic Lupus Erythematosus.

机构信息

University of Texas Medical Branch, Galveston, TX.

Department of Dermatopathology, Sagis, PLLC, Austin, TX.

出版信息

Am J Dermatopathol. 2020 Apr;42(4):280-282. doi: 10.1097/DAD.0000000000001518.

Abstract

Papulonodular mucinosis is a distinctive lupus erythematosus cutaneous variant that generally occurs in patients with systemic lupus erythematosus. Despite a higher incidence of SLE in women, lupus cutaneous mucinosis occurs more frequently in men. Typically, papulonodular mucinosis appears as asymptomatic, flesh-colored papules and nodules with a propensity for the trunk and upper extremities. Herein, we report a case of papulonodular mucinosis associated with systemic lupus erythematosus in a middle-aged woman. On presentation, patient had multiple flesh-colored papules coalescing into plaques on the trunk and upper extremities. Histological findings of the lesions demonstrated a pale dermis secondary to profuse mucin deposition. Immunofluorescent staining revealed a 'lupus band' with granular deposition of immunoglobulins/complement proteins at the dermal-epidermal junction.

摘要

结节性黏蛋白病是一种独特的红斑狼疮皮肤变异型,通常发生在系统性红斑狼疮患者中。尽管红斑狼疮在女性中的发病率更高,但狼疮性黏蛋白病在男性中更为常见。典型的结节性黏蛋白病表现为无症状的、肉色丘疹和结节,倾向于发生在躯干和上肢。在此,我们报告一例中年女性伴系统性红斑狼疮的结节性黏蛋白病。就诊时,患者躯干和上肢有多个肉色丘疹融合成斑块。病变的组织学发现显示真皮苍白,继发于大量黏蛋白沉积。免疫荧光染色显示在真皮-表皮交界处有“狼疮带”,免疫球蛋白/补体蛋白呈颗粒状沉积。

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