Jovanović M, Lenert P, Poljacki M, Mitic I, Duran V
Klinika za infektivne i dermatoveneroloske bolesti, Medicinski fakultet, Novi Sad.
Med Pregl. 1996;49(3-4):133-6.
A whole spectrum of various clinical and laboratory disorders in patients with skin changes, may present systemic disease manifestations. Serological parameters correlate with the progression of the disease. Authors present cases with unusual skin lesions and abnormal laboratory findings, that were presumed to be manifestations of the systemic disease progression. The first case is a report of a patient age 44, female with dermatomyositis that started suddenly from full health with generalized linear bluish dark erythematous lesion like excoriations, periocular heliotrope violaceous to dusky erythematous rash with edema in a symmetrical distribution involving periorbital skin with no pruritus, diagnosed on admission as the case of acute urticarica. In the second report, a 17-year old female was referred to us because of a spread up linear sclerodermia followed by high immunological disturbances. Our third case was a 21-year old female with a systemic lupus erythematous--Rowell syndrome, with skin lesions of erythema multiforme type with some similarities to dermatitis herpetiformis on the first examination.
患有皮肤病变的患者可能会出现一系列各种临床和实验室紊乱,并表现出全身性疾病症状。血清学参数与疾病进展相关。作者介绍了一些病例,这些病例有不寻常的皮肤病变和异常的实验室检查结果,推测为全身性疾病进展的表现。第一个病例报告的是一名44岁女性,患有皮肌炎,此前身体健康,突然发病,出现全身性线状蓝黑色红斑样擦伤,眼眶周围有紫红色至暗褐色红斑疹,并伴有水肿,对称分布于眶周皮肤,无瘙痒,入院时诊断为急性荨麻疹。在第二篇报告中,一名17岁女性因线状硬皮病扩散并伴有高度免疫紊乱被转诊至我们这里。我们的第三个病例是一名21岁女性,患有系统性红斑狼疮——罗威尔综合征,首次检查时有多形红斑型皮肤病变,与疱疹样皮炎有一些相似之处。