Bunker C B, Dowd P M
Department of Dermatology, University College and Middlesex Hospital School of Medicine, Middlesex Hospital, London, U.K.
Br J Dermatol. 1988 Jul;119(1):115-20. doi: 10.1111/j.1365-2133.1988.tb07112.x.
We describe a case of histologically proven giant cell arteritis (GCA) in a 62-year-old woman who initially presented with upper limb girdle pain and weakness, and intermittent claudication. Clinical improvement was obtained with oral prednisolone. She subsequently developed a photosensitive rash and was diagnosed as having systemic lupus erythematosus. The features of the two conditions and the possibility of an association are discussed.
我们描述了一例经组织学证实的巨细胞动脉炎(GCA)病例,患者为一名62岁女性,最初表现为上肢带疼痛、无力和间歇性跛行。口服泼尼松龙后临床症状有所改善。随后她出现了光敏性皮疹,并被诊断为系统性红斑狼疮。本文讨论了这两种疾病的特征以及两者关联的可能性。