Suppr超能文献

盘状红斑狼疮转变为肿胀性红斑狼疮1例报告

A case report of lupus erythematosus tumidus converted from discoid lupus erythematosus.

作者信息

Chen Xiaomei, Wang Sheng, Li Li

机构信息

Department of Dermatology, West China Hospital of Sichuan University, Chengdu, China.

出版信息

Medicine (Baltimore). 2018 Apr;97(16):e0375. doi: 10.1097/MD.0000000000010375.

Abstract

RATIONALE

Lupus erythematosus tumidus (LET) is an uncommon type of cutaneous lupus erythematosus (CLE) that is rarely associated with other forms of lupus erythematosus.

PATIENT CONCERNS

We report a 62-year-old Chinese man presented with recurrent erythematous facial plaques for 1 year and a low-grade fever for 1 week. He had been diagnosed as discoid lupus erythematosus (DLE) 1 year before. Physical examination showed diverse lesions, including prominent swelling of the eyelids, a few erythematous, edematous plaques on the left forehead, face, and neck, and 2 hairless macules. The histopathologic findings reveal liquefaction degeneration of the basal cells, perivascular, and periadnexal infiltration of lymphocytes, and interstitial mucin deposition in the superficial, and deep dermis.

DIAGNOSES

A diagnosis of LET was made on clinical and histological features.

INTERVENTIONS

The patient started treatment with prednisolone (1 mg/kg. d), combined with hydroxychloroquine (200 mg twice daily), and topical tacrolimus.

OUTCOMES

The cutaneous lesions completely cleared after a period of 3 months. No adverse effects or clinical evidence of recurrence had been found during the 6-month follow-up period.

LESSONS

We report a case of LET converted from DLE with diverse lesions, unusual pathologic findings and slow response to the treatment of corticosteroids combined with hydroxychloroquine. We speculate that a continuous spectrum may include DLE, LET, and systemic lupus erythematosus (SLE), these 3 entities could potentially, convert between each other.

摘要

理论依据

肿胀性红斑狼疮(LET)是一种罕见的皮肤型红斑狼疮(CLE),很少与其他形式的红斑狼疮相关。

患者情况

我们报告一名62岁中国男性,面部反复出现红斑斑块1年,低热1周。他1年前被诊断为盘状红斑狼疮(DLE)。体格检查发现多种皮损,包括眼睑明显肿胀,左侧前额、面部和颈部有一些红斑、水肿性斑块,以及2处无毛发斑。组织病理学检查结果显示基底细胞液化变性、血管周围和附件周围淋巴细胞浸润,以及浅表和深部真皮间质粘蛋白沉积。

诊断

根据临床和组织学特征诊断为LET。

干预措施

患者开始使用泼尼松龙(1mg/kg·d)联合羟氯喹(每日2次,每次200mg)及外用他克莫司治疗。

结果

3个月后皮肤损害完全消退。在6个月的随访期内未发现不良反应或复发的临床证据。

经验教训

我们报告一例由DLE转变为LET的病例,其具有多种皮损、不寻常的病理表现,对皮质类固醇联合羟氯喹治疗反应缓慢。我们推测一个连续谱可能包括DLE、LET和系统性红斑狼疮(SLE),这三种实体可能会相互转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db11/5916671/04432a341cb2/medi-97-e0375-g001.jpg

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