Ghosh Arghya P, Nag Falguni, Biswas Saugato, Rao Raghavendra, De Abhishek
Department of Dermatology, Bankura Sammilani Medical College, Bankura, West Bengal, India.
Department of Dermatology, Purulia Government Medical College, Purulia, West Bengal, India.
Indian J Dermatol. 2020 Jan-Feb;65(1):22-28. doi: 10.4103/ijd.IJD_282_19.
Lupus erythematosus (LE) is an autoimmune disorder with diverse clinical manifestations ranging from mild cutaneous disorder to life-threatening systemic illness and associated with varying immunological parameters.
We conducted a study in a tertiary care center of eastern India to determine the clinical pattern, immunological profile of patients with cutaneous manifestations of systemic LE (SLE) and their relationship with organ involvement.
Fifty-five consecutive patients attending dermatology OPD having features consistent with cutaneous LE and fulfilling the criteria of SLE were included. After proper history taking and clinical examination, routine blood and antinuclear antibody (ANA) profile, histopathological examination, and direct immunofluorescence test were undertaken.
Among 55 patients, 49 were female. ANA positivity was the most common association, followed by photosensitivity, malar rash, arthritis, oral ulcer, immunological markers, renal system involvement, discoid rash, serositis, central nervous system (CNS) involvement, and least common being the hematological involvement. Vacuolar basal cell degeneration was the commonest epidermal change and upper dermal periappendageal and perivascular lymphocytic infiltration was the commonest dermal change observed on histopathological examination. On direct immunofluorescence (DIF) granular pattern was seen in majority of patients. Statistically significant risk of kidney involvement was present both when patient had bullous lesions and DIF positivity of unexposed (DIF-UE) skin. CNS involvement was seen in five patients and it was found to be significantly associated with purpuric lesions.
This study reveals cutaneous lesions and DIF testing could be reliable predictors of systemic involvement and strongly suggests DIF testing, routinely in all patients of SLE.
红斑狼疮(LE)是一种自身免疫性疾病,临床表现多样,从轻度皮肤疾病到危及生命的全身性疾病不等,并与多种免疫参数相关。
我们在印度东部的一家三级医疗中心进行了一项研究,以确定系统性红斑狼疮(SLE)皮肤表现患者的临床模式、免疫特征及其与器官受累的关系。
纳入55例连续就诊于皮肤科门诊、具有符合皮肤LE特征且满足SLE标准的患者。在进行适当的病史采集和临床检查后,进行常规血液和抗核抗体(ANA)检测、组织病理学检查及直接免疫荧光试验。
55例患者中,49例为女性。ANA阳性是最常见的关联表现,其次是光敏性、颧部红斑、关节炎、口腔溃疡、免疫标志物、肾脏系统受累、盘状红斑、浆膜炎、中枢神经系统(CNS)受累,血液系统受累最不常见。空泡性基底细胞变性是最常见的表皮改变,真皮上部附属器周围和血管周围淋巴细胞浸润是组织病理学检查中最常见的真皮改变。直接免疫荧光(DIF)检查时,大多数患者可见颗粒状模式。当患者有大疱性皮损和未暴露皮肤的DIF阳性(DIF-UE)时,肾脏受累的风险具有统计学意义。5例患者出现CNS受累,发现其与紫癜性皮损显著相关。
本研究表明皮肤病变和DIF检测可能是系统性受累的可靠预测指标,并强烈建议对所有SLE患者常规进行DIF检测。