livedo reticularis/höfuðverkur

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Migraine is associated with livedo reticularis: a prospective study.

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OBJECTIVE To investigate the relationship of livedo reticularis, an ischemic dermatopathy, and migraine, an ischemic stroke risk factor. BACKGROUND Livedo reticularis refers to the reddish-blue reticular mottling of the skin resulting from narrowing of small and medium arteries at the

Congenital livedo reticularis and recurrent stroke-like episodes.

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Three children with pronounced livedo reticularis present since birth (cutis marmorata-telangiectasia congenita) have been followed to the ages of eight, 17 and 21 years. During childhood they developed frequent recurrent transient stroke-like hemipareses, affecting either side of the body,

Sneddon's syndrome presenting with severe disabling bilateral headache.

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Sneddon's syndrome is a rare vascular disease affecting mainly skin and brain arterioles leading to their occlusion due to excessive endothelial proliferation. The two main features of this syndrome are livedo reticularis and lacunar subcortical infarcts. Here, we describe the case of a 64-year-old

Livedo reticularis and migraine: a marker for stroke risk?

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OBJECTIVE Livedo reticularis is a dermatopathy characterized by an irregular, violaceous, netlike pattern which spares the face. Associated with a variety of conditions, it occurs consequent to pathological or physiological narrowing of small and medium arteries at the dermis-subcutis border.

Cluster headache is not associated with signs of a systemic inflammation.

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OBJECTIVE To investigate whether there is clinical or biochemical evidence for a transient systemic inflammation during active periods of cluster headache. METHODS Twenty-seven male and female consecutively selected patients with episodic cluster headache filled in questionnaires aiming at detecting

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

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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

Cerebral ischemic events associated with endocarditis, retinal vascular disease, and lupus anticoagulant.

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OBJECTIVE A group of young patients presenting with cerebral ischemic events, endocardial lesions, and lupus anticoagulant is described in order to highlight the common clinical laboratory features. METHODS Fourteen consecutive patients (10 females, age range 17 to 53 years [mean 38 years]) at onset

[Anti-phosphatidylethanolamine antibodies in patients with Sneddon's syndrome].

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Anti-phosphatidylethanolamine antibodies (aPE) belong to the group of anti-phospholipid antibodies (aPL) and are directed against neutral phospholipid, connected with co-factor protein, while cardiolipin antibodies (aKL) are directed against negative phospholipid. The paper presents a study of

Moyamoya syndrome associated with Sneddon's syndrome and antiphospholipid-protein antibodies.

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BACKGROUND There are anecdotal reports of the rare combination of Sneddon's syndrome, lupus anticoagulant, and Moyamoya. To our knowledge, we now report the first case of anticardiolipin antibodies, Sneddon's syndrome, and Moyamoya. METHODS Case-report and systematic literature review. RESULTS A

Systemic lupus erythematosus and hyper-eosinophilic syndrome: an unusual association.

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A 34-year old woman with dizziness, headache and both upper and lower extremities weakness was admitted to hospital. She had a history of photosensitivity but no asthma or allergy. On physical examination, malar rash and livedo reticularis were noted. White blood cell count was 18500/microL with

[Cerebral haemorrhage in Sneddon's syndrome: case report and literature review].

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BACKGROUND Sneddon's syndrome is the association between livedo reticularis and stroke. Hemorrhagic strokes in Sneddon's syndrome are exceptional. METHODS A 39-year-old woman who had had a livedo reticularis for about 14 years attended the Emergency Unit complaining of sudden, severe headache and

Altered hemostasis in migraineurs studied with a dynamic flow system.

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BACKGROUND Livedo reticularis (LR) refers to the violaceous netlike pattern of skin related to arteriopathy at the dermis-subcutis border. Livedo is associated with migraine, and among migraineurs, LR is more common in those with prior stroke. Other evidence of vascular perturbation in migraine

[Optic nerve infarction in Sneddon's syndrome].

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METHODS We report a case of a 26 year old woman with Raynaud's phenomenon and livedo reticularis 2 years onset, who presented with visual field defects accompanied by hypertension, hematuria, and headache. The examination revealed multiple retinal and optic nerve head infarcts in both

A rarely seen syndrome in rehabilitation of hemiplegia: antiphospholipid antibody-negative Sneddon's syndrome.

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Sneddon's syndrome is a rarely seen disorder and it is characterized by livedo reticularis (LR) and neurologic findings. Some systematic findings may also be seen with neurologic and cutaneous findings. In this case, we aimed to present a 28-year-old female patient with diffuse LR, cardiac valve

Sneddon's syndrome: another migraine-stroke association?

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Sneddon's syndrome refers to the enigmatic association of ischaemic stroke and livedo reticularis. We review the Sneddon's syndrome literature examining the association of this condition with headache, including migraine. Case reports and series are stratified into two groups based on headache

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