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伴有硬斑病样损害的红斑狼疮性脂膜炎

Lupus erythematosus panniculitis with morphea-like lesions.

作者信息

Stork J, Vosmík F

机构信息

2nd Department of Dermatology, Charles University, Prague, Czechoslovakia.

出版信息

Clin Exp Dermatol. 1994 Jan;19(1):79-82. doi: 10.1111/j.1365-2230.1994.tb01125.x.

Abstract

A 22-year-old female with morphea-like lesions, deep subcutaneous nodules and lipoatrophic areas of the skin on lateral aspects of the upper arms, on the breasts and on the buttocks is described. In 1990 a biopsy specimen obtained from a subcutaneous nodule showed hyaline necrosis of fat tissue; there were no epidermal changes. Direct immunofluorescence revealed granular deposits of IgM at the dermo-epidermal junction of the skin overlying the subcutaneous nodule. In a biopsy specimen taken at the onset of the disease in 1988, hyaline sclerosis of the deep dermis, follicular hyperkeratosis and vacuolar degeneration in the epidermis were described. There was weak positivity for antinuclear antibodies. The diagnosis of lupus erythematosus panniculitis (LEP) was made. Administration of chloroquine resulted in complete clearing of nodules in 3 months. The reported case demonstrates the difficulties in establishing the diagnosis of LEP in patients who present with subcutaneous disease, morphea-like lesions and who do not have other clinical or laboratory evidence of lupus erythematosus. The differential diagnosis of LEP and deep morphea is discussed.

摘要

本文描述了一名22岁女性,其在上臂外侧、乳房及臀部出现硬斑病样皮损、皮下深部结节及皮肤脂肪萎缩区。1990年,取自皮下结节的活检标本显示脂肪组织透明样坏死,未见表皮改变。直接免疫荧光显示皮下结节上方皮肤的真皮-表皮交界处有IgM颗粒状沉积。1988年疾病初发时所取活检标本显示真皮深层透明样硬化、毛囊角化过度及表皮空泡变性,抗核抗体弱阳性。诊断为狼疮性脂膜炎(LEP)。给予氯喹治疗3个月后结节完全消退。该病例报告表明,对于表现为皮下病变、硬斑病样皮损且无其他红斑狼疮临床或实验室证据的患者,确立LEP诊断存在困难。文中还讨论了LEP与深部硬斑病的鉴别诊断。

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