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Giant Aneurysm Arising from Anomalous Branch of the Middle Cerebral Artery in a Pediatric Patient: Case Report and Review of the Literature.
Wan, Kai Rui; Kirollos, Ramez W; Lee, Hwei Yee; Low, David C Y; Ng, Lee Ping; Seow, Wan Tew; Low, Sharon Y Y.
Afiliação
  • Wan KR; Neurosurgical Service, KK Women's and Children's Hospital, Singapore.
  • Kirollos RW; Neurosurgical Service, KK Women's and Children's Hospital, Singapore; Department of Neurosurgery, National Neuroscience Institute, Singapore; SingHealth Duke-NUS Neuroscience Academic Clinical Program, Singapore.
  • Lee HY; Department of Pathology, Tan Tock Seng Hospital, Singapore.
  • Low DCY; Neurosurgical Service, KK Women's and Children's Hospital, Singapore; Department of Neurosurgery, National Neuroscience Institute, Singapore; SingHealth Duke-NUS Neuroscience Academic Clinical Program, Singapore.
  • Ng LP; Neurosurgical Service, KK Women's and Children's Hospital, Singapore.
  • Seow WT; Neurosurgical Service, KK Women's and Children's Hospital, Singapore; Department of Neurosurgery, National Neuroscience Institute, Singapore; SingHealth Duke-NUS Neuroscience Academic Clinical Program, Singapore.
  • Low SYY; Neurosurgical Service, KK Women's and Children's Hospital, Singapore; Department of Neurosurgery, National Neuroscience Institute, Singapore; SingHealth Duke-NUS Neuroscience Academic Clinical Program, Singapore. Electronic address: sharon.low.y.y@singhealth.com.sg.
World Neurosurg ; 128: 165-168, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31082559
BACKGROUND: Pediatric intracranial aneurysms are extremely rare. In this age group, cerebral vascular anomalies have been associated with the development of intracranial aneurysms. CASE DESCRIPTION: We present a case of a previously well 11-year-old boy who presented with seizures secondary to a giant, unruptured, and partially thrombosed right middle cerebral artery (MCA) aneurysm. Extensive workup for underlying infective and autoimmune etiology was negative. Of interest, this vascular lesion was found to originate from an anomalous M2 branch, which ran an aberrant parallel course within the Sylvian fissure to the main and distally bifurcating MCA. The patient underwent successful surgical clipping and excision of the giant aneurysm. CONCLUSIONS: Because of the infrequency of the diagnosis, clinical presentation, and its unique neurovascular anatomy, the management of this case is discussed in corroboration with current literature. In addition, highlighting this unusual case in an individual adds to the growing body of literature for better disease understanding, especially in the pediatric population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Intracraniano / Artéria Cerebral Média / Trombose Intracraniana / Malformações Vasculares do Sistema Nervoso Central Limite: Child / Humans / Male Idioma: En Revista: World Neurosurg Assunto da revista: NEUROCIRURGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Singapura País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Intracraniano / Artéria Cerebral Média / Trombose Intracraniana / Malformações Vasculares do Sistema Nervoso Central Limite: Child / Humans / Male Idioma: En Revista: World Neurosurg Assunto da revista: NEUROCIRURGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Singapura País de publicação: Estados Unidos