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A 51-year-old man gave a 2-year history of worsening mobility, cognitive decline and headaches. He had a history of thromboembolic stroke, recurrent transient ischaemic attacks and a spontaneous intraventricular haemorrhage. On examination, he had livedo reticularis and perniosis and a systolic murmur. Catheter cerebral angiography showed peripheral small-vessel and medium-vessel vasculopathy resulting in pruning of the distal cortical vessels and tortuous irregular distal collaterals. Skin biopsy showed subtle vasculopathy with ectasia of capillaries and postcapillary venules but no frank vasculitis or arterial thrombosis. Repeated serum antiphospholipid antibody titres were negative. The clinical features, skin biopsy and angiogram findings strongly supported a diagnosis of Sneddon's syndrome. Clinicians should consider Sneddon's syndrome in patients with livedo reticularis and stroke. There are treatment dilemmas in this situation when ischaemic and haemorrhagic cerebral events coexist.
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http://dx.doi.org/10.1136/practneurol-2015-001341 | DOI Listing |
Oxf Med Case Reports
August 2025
Faculty of Medicine, Palestine Polytechnic University, Wadi Al-Hariyah Street, Hebron 9020000, Palestine.
Sneddon syndrome (SS) is a rare neurocutaneous disorder consisting of livedo racemosa (LR) and cerebrovascular disease with an incidence of 4 per 1 000 000 annually. It may be idiopathic or associated with autoimmune or genetic factors, including deficiency of adenosine deaminase 2 (DADA2). We describe a 17-month-old girl with recurrent fevers, hepatosplenomegaly, LR, and progressive liver fibrosis.
View Article and Find Full Text PDFRadiol Case Rep
September 2025
Department of Radiology and Interventional Imaging, CHU Hassan II, FEZ, Sidi Mohammed Ben Abdellah University, Fes, Morocco.
Sneddon's syndrome is a rare thrombotic vasculopathy characterized by the association of livedo racemosa and ischemic cerebrovascular events, typically affecting young to middle-aged women. We report the case of a 41-year-old woman who presented with sudden right-sided hemiparesis, expressive aphasia, and a history of livedo racemosa. MRI revealed bilateral ischemic lesions and cortical atrophy, while autoimmune and thrombophilia workups were negative.
View Article and Find Full Text PDFNeurology
April 2025
Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
J Cent Nerv Syst Dis
December 2024
Faculty of Medicine, The Hashemite University, Zarqa, Jordan.
Background: Sneddon's syndrome is a rare thrombotic vasculopathy characterized by the coexistence of both cerebrovascular events and livedo reticularis.
Objective: This review aims to raise awareness among physicians by discussing the whole clinical spectrum of the disease. Typically, Sneddon syndrome presents in middle-aged women with a cerebrovascular accident and a preexisting skin rash, which is livedo reticularis.
[This corrects the article DOI: 10.1371/journal.pone.
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