Sneddon syndrome and the diagnostic value of skin biopsies - Three young patients with intracerebral lesions and livedo racemosa

被引:16
作者
Legierse, Catharina M. [1 ]
Dijk, Marijke R. Canninga-Van [2 ]
Bruijnzeel-Koomen, Carla A. F. M. [3 ]
Kuck-Koot, Veronica C. M. [3 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Dermatol, NL-1100 DE Amsterdam, Netherlands
[2] Univ Med Ctr, Dept Pathol, Utrecht, Netherlands
[3] Univ Med Ctr, Dept Dermatol, Utrecht, Netherlands
关键词
antiphospholipid antibody syndrome; diagnosis; livedo racemosa; skin biopsy; Sneddon syndrome;
D O I
10.1684/ejd.2008.0397
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Sneddon syndrome is a rare disorder characterised by generalised livedo racemosa of the skin with extracutaneous neurological symptoms like headache, vertigo, transient ischaemic attacks (TIA), stroke, and seizures. Diagnosis of Sneddon syndrome is based on these clinical features and positive findings in skin biopsies, namely the histological proof of occlusion of arterioles by intimal proliferation. We describe three cases of young patients with clinical characteristics of Sneddon syndrome, but in only two cases could this diagnosis be confirmed by skin biopsies. These cases stress the difficulty of diagnosing Sneddon syndrome and show the additive value of skin biopsies in this process.
引用
收藏
页码:322 / 328
页数:7
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