Palavras-chave
anemia de células falciformes
síndrome
Como Citar
Resumo
El síndrome de moyamoya es una rara entidad oclusiva que afecta los vasos cerebrales. Es predominante de la población japonesa, de donde se creía inicialmente era exclusiva; pero hoy en día se han reportado casos en todo el mundo y en diferentes grupos étnicos. Consiste en la oclusión crónica y progresiva de la circulación cerebral anterior con la consecuente aparición de colaterales que da un patrón imaginológico en arteriografía, similar a una “nube de humo”; de ahí su nombre en japonés moyamoya. En este artículo se reporta el caso de un paciente pediátrico femenino de raza negra con antecedente de anemia de células falciformes con imágenes representativas.
Suzuki J, Takaku A. Cerebrovascular “moyamoya” disease: disease showing abnormal net-like vessels in base of brain. Arch Neurol. 1969;20(3):288-99.
Scott RM, Smith ER. Moyamoya disease and moyamoya syndrome. N Engl J Med. 2009;360:1226-37.
Janda PH, Bellew JG, Veerappan V. Moyamoya disease: case report and literature review. J Am Osteopath Assoc. 2009;109(10):547-53.
Yamashita M, Oka K, Tanaka K. Cervicocephalic arterial thrombi and thromboemboli in moyamoya d-possible correlation with progressive intimal thickening in the intracranial major arteries. Stroke. 1984;15:264-70.
Stockman JA, Nigro MA, Mishkin MM, Oski FA. Occlusion of large cerebral vessels in sickle-cell anemia. N Engl J Med. 1972;287:846-9.
Houkin K, Iihoshi S, Mikami T. Moyamoya desease update. Part VII: Morphological imaging. Tokio: Springer; 2010. p. 140-57.
Merkel KHH, Ginsberg PL, Parker JC, Donovan MJ. Cerebrovascular disease in sickle cell anemia: a clinical, pathological and radiological correlation. Stroke. 1978,9:45-52.
Chang SD, Steinberg GK. Surgical management of moyamoya disease [internet]. [Citado dic 2011]. Disponible en http://www.moyamoya.com/journals/moyamoya.html.
This journal is registered under a Creative Commons Attribution 4.0 International Public License. Thus, this work may be reproduced, distributed, and publicly shared in digital format, as long as the names of the authors and Pontificia Universidad Javeriana are acknowledged. Others are allowed to quote, adapt, transform, auto-archive, republish, and create based on this material, for any purpose (even commercial ones), provided the authorship is duly acknowledged, a link to the original work is provided, and it is specified if changes have been made. Pontificia Universidad Javeriana does not hold the rights of published works and the authors are solely responsible for the contents of their works; they keep the moral, intellectual, privacy, and publicity rights.
Approving the intervention of the work (review, copy-editing, translation, layout) and the following outreach, are granted through an use license and not through an assignment of rights. This means the journal and Pontificia Universidad Javeriana cannot be held responsible for any ethical malpractice by the authors. As a consequence of the protection granted by the use license, the journal is not required to publish recantations or modify information already published, unless the errata stems from the editorial management process. Publishing contents in this journal does not generate royalties for contributors.