Suppr超能文献

儿童线状硬皮病样深部红斑狼疮

Linear Sclerodermoid Lupus Erythematosus Profundus in a Child.

作者信息

Elbendary Amira, Griffin John, Li Suzanne, Tlougan Brook, Junkins-Hopkins Jacqueline M

机构信息

*Ackerman Academy of Dermatopathology, New York, NY; †Department of Dermatology, Kasr Alainy Faculty of Medicine, Cairo University, Giza, Egypt; ‡Departments of Internal Medicine and Pathology and Laboratory Medicine, Texas A&M University Health Science Center, Dallas, TX; §Department of Pediatrics, Joseph M. Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, NJ; and ¶Department of Dermatology, New York Presbyterian Hospital, Columbia University Medical Center, New York, NY.

出版信息

Am J Dermatopathol. 2016 Dec;38(12):904-909. doi: 10.1097/DAD.0000000000000663.

Abstract

Lupus erythematosus panniculitis, also known as lupus profundus, is a variant in the clinicopathological spectrum of lupus erythematosus (LE) affecting about 2%-3% of LE patients. A linear configuration of LE panniculitis has been reported rarely with rare reports describing the coexistence of different forms of cutaneous LE and localized morphea. In this study, the authors present a 9-year-old girl with linear arrangement of subcutaneous nodules on her left forearm. Microscopic findings from 2 biopsies included lymphocytes at the dermoepidermal junction with mild interface dermatitis, a dense lymphocytic infiltrate that was concentrated around adnexae and subcutaneous fat in concert with thickened collagen bundles and mild widening of fibrous septae surrounding fat lobules. Although the clinical differential diagnosis included panniculitis or a sporotrichoid infection, 1 biopsy showed a dense lymphocytic infiltrate histologically bordered on that of cutaneous lymphoid hyperplasia or a late stage of Lyme disease, and a second also demonstrated more prominent sclerodermoid collagen bundles rendering the diagnosis of linear sclerodermoid LE profundus.

摘要

狼疮性脂膜炎,也称为深部狼疮,是红斑狼疮(LE)临床病理谱中的一种变体,约占LE患者的2%-3%。线性排列的狼疮性脂膜炎报道很少,仅有罕见报道描述了不同形式的皮肤型LE与局限性硬斑病并存。在本研究中,作者报告了一名9岁女孩,其左前臂出现皮下结节呈线性排列。两次活检的显微镜检查结果显示,真皮表皮交界处有淋巴细胞,伴有轻度界面性皮炎,致密的淋巴细胞浸润集中在附属器和皮下脂肪周围,同时胶原束增厚,脂肪小叶周围的纤维间隔轻度增宽。尽管临床鉴别诊断包括脂膜炎或孢子丝菌样感染,但一次活检显示组织学上致密的淋巴细胞浸润与皮肤淋巴细胞增生或莱姆病晚期相近,另一次活检也显示出更明显的硬皮病样胶原束,从而诊断为线性硬皮病样深部狼疮。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验