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Huge interparietal posterior fontanel meningohydroencephalocele.
Rosildo, Jorge Félix Companioni; Dos Santos, Manuel Filipe Dias; de Santa Barbara, Rita de Cassia.
Afiliação
  • Rosildo JF; Department of Neurosurgery - Clínica Multiperfil, Luanda - Angola .
  • Dos Santos MF; Department of Neurosurgery - Clínica Multiperfil, Luanda - Angola .
  • de Santa Barbara Rde C; Department of Physiotherapy - Clínica Multiperfil, Luanda - Angola .
Autops Case Rep ; 5(1): 43-8, 2015.
Article em En | MEDLINE | ID: mdl-26484324
Congenital encephalocele is a neural tube defect characterized by a sac-like protrusion of the brain, meninges, and other intracranial structures through the skull, which is caused by an embryonic development abnormality. The most common location is at the occipital bone, and its incidence varies according to different world regions. We report a case of an 1-month and 7-day-old male child with a huge interparietal-posterior fontanel meningohydroencephalocele, a rare occurrence. Physical examination and volumetric computed tomography were diagnostic. The encephalocele was surgically resected. Intradural and extradural approaches were performed; the bone defect was not primarily closed. Two days after surgery, the patient developed hydrocephaly requiring ventriculoperitoneal shunting. The surgical treatment of the meningohydroencephalocele of the interparietal-posterior fontanel may be accompanied by technical challenges and followed by complications due to the presence of large blood vessels under the overlying skin. In these cases, huge sacs herniate through large bone defects including meninges, brain, and blood vessels. The latter present communication with the superior sagittal sinus and ventricular system. A favorable surgical outcome generally follows an accurate strategy taking into account individual features of the lesion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Autops Case Rep Ano de publicação: 2015 Tipo de documento: Article País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Autops Case Rep Ano de publicação: 2015 Tipo de documento: Article País de publicação: Brasil