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亚急性皮肤型红斑狼疮中的白细胞破碎性血管炎:3例临床病理研究及文献复习

Leukocytoclastic vasculitis in subacute cutaneous lupus erythematosus: clinicopathologic study of three cases and review of the literature.

作者信息

Sánchez-Pérez J, Peñas P F, Ríos-Buceta L, Fernández-Herrera J, Fraga J, García-Díez A

机构信息

Department of Dermatology, Hospital Universitario de la Princesa, Universidad Autónoma, Madrid, España.

出版信息

Dermatology. 1996;193(3):230-5. doi: 10.1159/000246251.

Abstract

BACKGROUND

Leukocytoclastic vasculitis associated with subacute cutaneous lupus erythematosus (SCLE) was observed by Sontheimer et al. in their first clinical series of patients with SCLE, although recent reports have suggested that its frequency was rare.

OBJECTIVE

To evaluate the prevalence of cutaneous leukocytoclastic vasculitis (CLV) in patients with SCLE and to describe the clinicopathologic manifestations, response to treatment and prognosis of this subgroup of patients.

METHODS

We reviewed all cases of SCLE seen at the Hospital de la Princesa from 1980 to 1995.

RESULTS

Three (9%) of our 27 patients with SCLE exhibited CLV and SCLE. Purpura, maculoerythematous lesions, urticaria, nodules and necrotic lesions on the leg, trunk and palmoplantar regions were present in our patients with CLV and SCLE. Histologically, SCLE-associated CLV was a small-sized vessel leukocytoclastic vasculitis with intravascular thrombosis in the deep dermis and coexistence of lesions of CLV and SCLE.

CONCLUSION

In our patients, CLV was self-limited and not associated with a worsened prognosis, with only cutaneous involvement in their further relapses of SCLE.

摘要

背景

Sontheimer等人在他们首个亚急性皮肤型红斑狼疮(SCLE)患者临床系列中观察到与亚急性皮肤型红斑狼疮相关的白细胞破碎性血管炎,尽管近期报告表明其发生率很低。

目的

评估SCLE患者中皮肤白细胞破碎性血管炎(CLV)的患病率,并描述该亚组患者的临床病理表现、治疗反应及预后。

方法

我们回顾了1980年至1995年在公主医院就诊的所有SCLE病例。

结果

我们的27例SCLE患者中有3例(9%)出现CLV和SCLE。CLV合并SCLE患者的腿部、躯干和掌跖部位出现紫癜、斑丘疹、荨麻疹、结节及坏死性皮损。组织学上,与SCLE相关的CLV是一种小血管白细胞破碎性血管炎,在真皮深层有血管内血栓形成,且CLV和SCLE病变共存。

结论

在我们的患者中,CLV为自限性,与预后恶化无关,在SCLE进一步复发时仅累及皮肤。

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