livedo reticularis/insultas

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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,

Livedo reticularis and cerebrovascular accidents.

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Livedo reticularis is a clinical pattern of cutaneous vascular involvement that can be seen in association with many diseases. The association of livedo reticularis and cerebrovascular accidents has been reported rarely in the past. We report on a 52-year-old woman with marked generalized livedo

Livedo reticularis and cerebrovascular accidents (Sneddon's syndrome) as a clinical expression of antiphospholipid syndrome.

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We present two patients with livedo reticularis and cerebrovascular accidents (Sneddon's syndrome) and positive anticardiolipin antibodies. We suggest that these antibodies may be pathophysiologically related to the clinical manifestation observed in some patients with this syndrome. When Sneddon's

Livedo reticularis, developmental delay and stroke-like episode in a 7-year-old male.

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Livedo reticularis is a vascular abnormality of the skin resulting in an erythematous reticular rash. The combination of livedo reticularis and stroke-like episodes in adults is known as Sneddon syndrome [Sneddon, IB (1965). Br J Dermatol 77:180-188]. A similar combination of stroke-like episodes

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.

[Livedo reticularis and cerebrovascular accidents].

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The authors report the case of three middle-aged women admitted to the hospital because of cerebro-vascular accidents, in whom examination disclosed idiopathic livedo reticularis. This association has only been described recently, but does not seem fortuitous; some of the clinical manifestations are

Anticardiolipin antibodies, livedo reticularis, and cerebrovascular accidents in SLE.

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[Idiopathic livedo reticularis and cerebrovascular accidents (Sneddon syndrome)].

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Congenital livedo reticularis and recurrent strokes in two unrelated young children.

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[Livedo reticularis and cerebrovascular accidents (Sneddon syndrome)].

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Gonadotrophins, livedo reticularis, and strokes.

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Seizures in primary antiphospholipid syndrome: the relevance of smoking to stroke.

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OBJECTIVE To evaluate the frequency of seizures in primary antiphospholipid syndrome (PAPS) and their possible clinical and laboratory associations. METHODS Eighty-eight PAPS patients (Sydney's criteria) were analyzed by a standard interview, physical examination and review of medical charts. Risk

Cerebrovascular lesions and livedo reticularis (Sneddon's syndrome)--a progressive cerebrovascular disorder?

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Four cases are described in which livedo reticularis was associated with repeated cerebrovascular accidents, which eventually resulted in severe disability in two cases. Patients with severe disability had a history of many years, whereas two patients with little or moderate residual disability had

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

The spectrum of livedo reticularis and anticardiolipin antibodies.

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We document a study of 65 patients presenting to our clinics, over a 2-year period, with livedo reticularis. All patients were screened for the presence of anti-cardiolipin antibodies and assessed for the presence of central nervous system disease and features of the 'antiphospholipid' syndrome,

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