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Endoscopic third ventriculostomy to treat hydrocephalus associated with macrocephaly-cutis marmorata telangiectatica congenita.

Abstract
Macrocephaly-cutis marmorata telangiectatica congenita is a rare overgrowth syndrome commonly associated with hydrocephalus. Although the pathophysiological characteristics of the hydrocephalus in this syndrome is not fully known, previous reports have described its treatment with ventriculoperitoneal shunt placement. The authors describe 2 cases of macrocephaly-cutis marmorata telangiectatica congenita successfully treated for progressive hydrocephalus with endoscopic third ventriculostomy. Both patients experienced clinical and radiographic stabilization following treatment, and these findings offer insight into the pathophysiology of the hydrocephalus and its ideal management.
AuthorsAlim P Mitha, Kelly J Bullivant, Julie L Lauzon, Walter J Hader
JournalJournal of neurosurgery. Pediatrics (J Neurosurg Pediatr) Vol. 4 Issue 4 Pg. 397-401 (Oct 2009) ISSN: 1933-0715 [Electronic] United States
PMID19795974 (Publication Type: Case Reports, Journal Article)
Topics
  • Abnormalities, Multiple (diagnosis)
  • Cephalometry
  • Cerebellum (pathology)
  • Disease Progression
  • Encephalocele (diagnosis, etiology, surgery)
  • Female
  • Humans
  • Hydrocephalus (diagnosis, etiology, surgery)
  • Infant
  • Magnetic Resonance Angiography
  • Magnetic Resonance Imaging
  • Magnetic Resonance Imaging, Cine
  • Male
  • Syndrome
  • Telangiectasis (congenital)
  • Third Ventricle (surgery)
  • Tomography, X-Ray Computed
  • Ventriculostomy (methods)

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