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Livedo racemosa generalisata and stroke
Clinical Neurology and Neurosurgery, 1985The authors describe three young female patients with generalized livedo racemosa and cerebral infarction. The radiologic and biopsy findings point to a widespread vasculopathy, involving small and mid-sized arteries. The histologic examination of the temporal artery biopsy in two patients gives additional evidence for a chronic endarteritis as ...
E Van de Velde
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Intracerebral hemorrhage associated with livedo racemosa
Journal of Stroke and Cerebrovascular Diseases, 2000We report on a case of intracerebral hemorrhage associated with livedo racemosa in a 13-year-old girl. A skin biopsy specimen showed endothelitis and mixed inflammatory cellular infiltrate around the small arteries. We believe that the cerebral hemorrhage might have been caused by fragility of the intracranial small arteries and that this case could be
Fumiharu Kimura
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Journal of Neurology, 2005
Livedo is a cutaneous sign of striking violaceous netlike patterned erythema of the skin. This dermatological phenomenon is of special interest in the differential diagnosis in neurological patients. In 1907 Ehrmann distinguished two different patterns of livedo: the pathological livedo racemosa and the physiological livedo reticularis.
Markus Kraemer +2 more
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Livedo is a cutaneous sign of striking violaceous netlike patterned erythema of the skin. This dermatological phenomenon is of special interest in the differential diagnosis in neurological patients. In 1907 Ehrmann distinguished two different patterns of livedo: the pathological livedo racemosa and the physiological livedo reticularis.
Markus Kraemer +2 more
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Clinical and Experimental Dermatology, 2023
A 41-year-old woman with monoclonal gammopathy of undetermined significance presented with a 1-year history of livedo racemosa that started on one arm after receiving the Pfizer BioNTech COVID-19 vaccine. Her primary care physician initially thought it was a benign reaction to the COVID-19 vaccine as her symptoms were on the same arm as the site of ...
Patricia Zhao +5 more
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A 41-year-old woman with monoclonal gammopathy of undetermined significance presented with a 1-year history of livedo racemosa that started on one arm after receiving the Pfizer BioNTech COVID-19 vaccine. Her primary care physician initially thought it was a benign reaction to the COVID-19 vaccine as her symptoms were on the same arm as the site of ...
Patricia Zhao +5 more
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Amantadine-Induced Livedo Racemosa
The International Journal of Lower Extremity Wounds, 2015Although livedo reticularis is a known adverse effect of amantadine, only limited studies have addressed this association. Livedo racemosa in contrast to livedo reticularis is characterized by a striking violaceous netlike pattern of the skin similar to livedo reticularis with a different histopathology and morphology (irregular, broken circular ...
Paulo Ricardo, Criado +3 more
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Livedo racemosa presenting with congenital fibromuscular dysplasia
British Journal of Dermatology, 2010Teruhiko Makino +2 more
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Livedo racemosa: A Report of Five Cases
Dermatology, 2009We present 5 patients in whom the diagnosis of livedo racemosa gave rise to clinical and laboratory investigations revealing arterial disease of different etiologies. This presentation emphasizes the importance of not missing the clinical diagnosis of livedo racemosa.
Zala L, Braathen LR
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Livedo racemosa bei primärem Antiphospholipidsyndrom
Aktuelle Dermatologie, 2021ZusammenfassungDas Antiphospholipidsyndrom umfasst als Kardinalsymptome rezidivierende arteriovenöse thrombembolische Ereignisse, vermehrte Aborte oder Schwangerschaftskomplikationen und das Vorliegen von Antiphospholipid-Antikörpern. In ca. 20 % der Fälle liegt eine Livedo racemosa als kutane Manifestation vor.
E. Oms, M. Tronnier
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HNO, 1986
Livedo racemosa is a very rare disease with an idiopathic and symptomatic form. The diagnosis is very difficult to make because many primary diseases are responsible. Skin reactions show no typical form and range from urticarial nodules and purpuriform papillae to ulceration.
J, Lindemann, K G, Rose
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Livedo racemosa is a very rare disease with an idiopathic and symptomatic form. The diagnosis is very difficult to make because many primary diseases are responsible. Skin reactions show no typical form and range from urticarial nodules and purpuriform papillae to ulceration.
J, Lindemann, K G, Rose
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Livedo racemosa generalisata: An evaluation of thirty-four cases
Journal of the American Academy of Dermatology, 1990The results of investigations in 34 patients (28 women, 6 men) with livedo racemosa generalisata are presented. Neurologic or psychiatric symptoms were present in 28 patients. Nineteen patients had had one or more cerebral infarctions, and epilepsy (Sneddon's syndrome) developed in six. In most cases livedo preceded the neurologic disorder. In addition,
D, Lubach +5 more
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