Parodi A, Caproni M, Cardinali C, Bernacchi E, Fuligni A, De Panfilis G, Zane C, Papini M, Veller F C, Vaccaro M, Fabbri P
Sezione di Dermatologia, Università di Genova, DISEM, Genova, Italia.
Dermatology. 2000;200(1):6-10. doi: 10.1159/000018307.
Subacute cutaneous lupus erythematosus (SCLE) is a distinct subset of cutaneous lupus erythematosus clinically characterized by psoriasiform and/or annular lesions and by a mild or absent systemic involvement.
The Italian Group of Immunodermatology of the Italian Society of Dermatology and Venereology reviewed the cases of SCLE seen in 10 years (1987-1996).
Forty-six women and 12 men have been retrospectively studied, 42% had annular lesions, 39% psoriasiform ones and 16% both.
Lesions were mainly localized on the neck and face and relapsed in spring and autumn. Seventeen patients had 4 or more American College of Rheumatology criteria and could be classified as having systemic lupus erythematosus. The most frequent histopathological alterations were epidermal atrophy, hydropic degeneration of the basal layer and perivascular lymphocytic infiltrate. Deposits of immunoglobulins and C3 at the dermo-epidermal junction on the clinically involved skin were present in 86% of the patients. Dust-like particles in the epidermis were only found in 3% of cases. Anti-Ro/SSA antibodies were found in 71% of the cases and anti-dsDNA only in 5% of cases.
SCLE is a particular subset of cutaneous lupus erythematosus with peculiar clinical and immunopathological features.
亚急性皮肤型红斑狼疮(SCLE)是皮肤型红斑狼疮的一个独特亚型,临床上以银屑病样和/或环形皮损为特征,全身受累轻微或无全身受累。
意大利皮肤病与性病学会免疫皮肤病学意大利小组回顾了10年(1987 - 1996年)间所见的SCLE病例。
对46名女性和12名男性进行了回顾性研究,42%有环形皮损,39%有银屑病样皮损,16%两者皆有。
皮损主要位于颈部和面部,在春秋季复发。17名患者有4项或更多美国风湿病学会标准,可归类为患有系统性红斑狼疮。最常见的组织病理学改变是表皮萎缩、基底层细胞水肿变性和血管周围淋巴细胞浸润。86%的患者在临床受累皮肤上的真皮 - 表皮交界处有免疫球蛋白和C3沉积。仅3%的病例在表皮中发现尘样颗粒。71%的病例发现抗Ro/SSA抗体,仅5%的病例发现抗双链DNA抗体。
SCLE是皮肤型红斑狼疮的一个特殊亚型,具有独特的临床和免疫病理学特征。