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Lupus profundus limited to a site of trauma: Case report and review of the literature.局限于创伤部位的深部狼疮:病例报告及文献复习
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Intravenous immunoglobulin in lupus panniculitis.静脉注射免疫球蛋白治疗狼疮性脂膜炎。
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[Lupus panniculitis in adolescence].青少年狼疮性脂膜炎
Hautarzt. 2007 Nov;58(11):920-2. doi: 10.1007/s00105-007-1412-z.
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The dynamism of cutaneous lupus erythematosus: mild discoid lupus erythematosus evolving into SLE with SCLE and treatment-resistant lupus panniculitis.皮肤型红斑狼疮的动态变化:轻度盘状红斑狼疮演变为伴亚急性皮肤型红斑狼疮的系统性红斑狼疮及治疗抵抗性狼疮性脂膜炎。
Clin Rheumatol. 2007 Jul;26(7):1176-9. doi: 10.1007/s10067-006-0310-6. Epub 2006 Apr 28.
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[Connective tissue diseases in childhood].
Hautarzt. 2005 Oct;56(10):925-36. doi: 10.1007/s00105-005-1016-4.

儿童盘状红斑狼疮和深部红斑狼疮:两例报告。

Discoid lupus erythematosus and lupus profundus in childhood: a report of two cases.

作者信息

Wimmershoff M B, Hohenleutner U, Landthaler M

机构信息

Department of Dermatology, University of Regensburg, Germany.

出版信息

Pediatr Dermatol. 2003 Mar-Apr;20(2):140-5. doi: 10.1046/j.1525-1470.2003.20210.x.

DOI:10.1046/j.1525-1470.2003.20210.x
PMID:12657012
Abstract

Discoid lupus erythematosus (DLE) is a rare disorder in childhood, with 22 cases reported in the English-language literature. Less than 2% of patients with DLE have an onset before 10 years of age. We describe two children with DLE and lupus profundus with an onset of the disease at the ages of 11 and 15 years and focus on likely histopathologic differences between DLE in children and in adults. Histopathologic characteristics for childhood DLE might be an intense periadnexal and perivascular infiltrate extending into the interstitium and subcutaneous tissue consisting of lymphocytes, histiocytes, eosinophilic granulocytes, and plasma cells and lacking epidermal atrophy. The diagnosis of DLE in our two patients was established by clinicopathologic correlation based on clinical presentation, histologic and immunofluorescent findings in skin biopsy specimens, and the absence of clinical and laboratory evidence of systemic involvement. Therapy with antimalarials resulted in reduction of the skin lesions, but in one patient severe lipoatrophy occurred.

摘要

盘状红斑狼疮(DLE)在儿童期是一种罕见疾病,英文文献中报道了22例。DLE患者中不到2%在10岁之前发病。我们描述了两名分别在11岁和15岁发病的患有DLE和深部狼疮的儿童,并重点关注儿童和成人DLE可能存在的组织病理学差异。儿童DLE的组织病理学特征可能是围绕附属器和血管周围有强烈浸润,延伸至间质和皮下组织,浸润细胞包括淋巴细胞、组织细胞、嗜酸性粒细胞和浆细胞,且无表皮萎缩。我们这两名患者的DLE诊断是通过临床病理相关性确定的,依据临床表现、皮肤活检标本的组织学和免疫荧光结果,以及无系统性受累的临床和实验室证据。抗疟药治疗使皮肤病变减轻,但其中一名患者出现了严重的脂肪萎缩。