Intracranial intraaxial cerebral tufted angioma: case report

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منابع مشابه

CASE REPORT Tufted angioma and myofascial pain syndrome

Tufted angioma is a rare acquired vascular tumor. It is characterized by painful purplish macules that may progress to plaques containing angiomatous papules. The condition is benign; however, it often affects extensive areas of the skin, leading to functional disability of the affected limb if painful. The present report describes a case of a tufted angioma associated with myofascial pain synd...

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Tufted angioma*

©2017 by Anais Brasileiros de Dermatologia Dear Editor, Tufted angioma is a rare vascular tumor, with slow angiomatous proliferation, usually located in the skin and subcutaneous tissue. Its clinical presentation is of a solitary angiomatous tumor, usually located on the neck, upper trunk and extremities. It is more frequent in children, with no sex or racial predilection. The term tufted angio...

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Congenital giant tufted angioma.

668 defined, hemispherical, nontender, noncompressible, boggy swelling, abutting the lower margin of the plaque. A few satellite, hyperpigmented papules were present over the thighs in the periphery of the main lesion. The patient denied any history of bleeding or ulceration of the plaque. There was no evidence of sweating or excessive growth of lanugo hair over the plaque. Thrill and bruit wer...

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[Congenital self-limiting tufted angioma].

1. Izikson L, English JC 3rd, Zirwas MJ. The flushing patient: differential diagnosis, workup, and treatment. J Am Acad Dermatol. 2006;55:193-208. 2. Lubbe J, Milingou M. Images in clinical medicine. Tacrolimus ointment, alcohol, and facial flushing. N Engl J Med. 2004;351:2740. 3. Sticherling M, Brasch J. Alcohol: intolerance syndromes, urticarial and anaphylactoid reactions. Clin Dermatol. 19...

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Congenital, self-regressing tufted angioma.

BACKGROUND Tufted angioma (known in Japanese literature as angioblastoma of Nakagawa) is an uncommon, histologically benign, vascular tumor. Lesions typically present during infancy or early childhood and are most commonly reported to persist and/or expand over time. Congenital presentations are rare, as are reports of spontaneous regression. OBSERVATIONS We present a series of 5 histopatholo...

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ژورنال

عنوان ژورنال: Journal of Neurosurgery

سال: 2018

ISSN: 0022-3085,1933-0693

DOI: 10.3171/2016.10.jns162207