Literature DB >> 19795974

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

Alim P Mitha1, Kelly J Bullivant, Julie L Lauzon, Walter J Hader.   

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.

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Year:  2009        PMID: 19795974     DOI: 10.3171/2008.12.PEDS088

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  2 in total

1.  Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3.

Authors:  Atsuko Harada; Fuyuki Miya; Hidetsuna Utsunomiya; Mitsuhiro Kato; Takumi Yamanaka; Tatsuhiko Tsunoda; Kenjiro Kosaki; Yonehiro Kanemura; Mami Yamasaki
Journal:  Childs Nerv Syst       Date:  2014-11-22       Impact factor: 1.475

Review 2.  Megalencephaly-capillary malformation syndrome and associated hydrocephalus: treatment options and revision of the literature.

Authors:  M Alamar; S Candela; A Flor-Goikoetxea; H Salvador; A F Martinez-Monseny; J Muchart; J Hinojosa
Journal:  Childs Nerv Syst       Date:  2021-05-28       Impact factor: 1.475

  2 in total

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