Komócsi A, Tóvari E, Pajor L, Czirják L
2nd Department of Internal Medicine, University of Pécs, Medical Faculty, Hungary.
J Eur Acad Dermatol Venereol. 2001 Sep;15(5):476-80. doi: 10.1046/j.1468-3083.2001.00310.x.
Necrotizing histiocytic lymphadenopathy (NHL) is a rarely observed clinical entity that is occasionally associated with systemic lupus erythematosus (SLE). The histological features of the condition have been considered to be indistinguishable from those of lymphadenitis in subjects with SLE, and the clinical symptoms of the two disorders share common features. This report presents the case history of a subject who developed SLE with central nervous system involvement 3 years following onset of Kikuchi's disease (histiocytic necrotizing lymphadenitis). Repeated lymph node biopsies confirmed the diagnosis in relation to the clinical progression. A review of the literature on this topic is also presented.
坏死性组织细胞性淋巴结病(NHL)是一种罕见的临床病症,偶尔与系统性红斑狼疮(SLE)相关。该病症的组织学特征被认为与SLE患者的淋巴结炎无法区分,且这两种疾病的临床症状有共同特征。本报告介绍了一名患者的病史,该患者在菊池病(组织细胞性坏死性淋巴结炎)发病3年后出现了累及中枢神经系统的SLE。反复的淋巴结活检根据临床进展确诊了病情。本文还对该主题的文献进行了综述。