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斯内登综合征:一切都与外胚层有关。

Sneddon's syndrome: it is all in the ectoderm.

作者信息

Rutter-Locher Zoe, Chen Zhongbo, Flores Lorena, Basu Tanya, Creamer Daniel, Weeks Robert, Arya Roopen, Nashef Lina

机构信息

Department of Neurology, King's College Hospital, London, UK.

Department of Dermatology, King's College Hospital, London, UK.

出版信息

Pract Neurol. 2016 Aug;16(4):300-3. doi: 10.1136/practneurol-2015-001341. Epub 2016 Mar 11.

Abstract

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.

摘要

一名51岁男性有2年行动能力恶化、认知衰退和头痛的病史。他有血栓栓塞性中风、复发性短暂性脑缺血发作和自发性脑室内出血病史。检查时,他有网状青斑和冻疮以及收缩期杂音。导管脑血管造影显示外周小血管和中血管血管病变,导致远端皮质血管变细和远端侧支血管迂曲不规则。皮肤活检显示有毛细血管和毛细血管后微静脉扩张的轻微血管病变,但无明显血管炎或动脉血栓形成。反复检测血清抗磷脂抗体滴度均为阴性。临床特征、皮肤活检和血管造影结果强烈支持斯内登综合征的诊断。临床医生在患有网状青斑和中风的患者中应考虑斯内登综合征。当缺血性和出血性脑事件并存时,这种情况存在治疗困境。

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