Literature DB >> 34047857

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

M Alamar1, S Candela2, A Flor-Goikoetxea3, H Salvador4, A F Martinez-Monseny5, J Muchart6, J Hinojosa2.   

Abstract

PURPOSE: We describe our series of 4 patients with megalencephaly-capillary malformation syndrome (MCAP) and review the literature in order to assess the optimal treatment for the associated hydrocephalus.
METHODS: We review our institutional series of hydrocephalus associated with MCAP and review the literature, analyzing the causes that could originate the hydrocephalus and the different types of treatments proposed for them.
RESULTS: Of our patients treated with ventriculoperitoneal (VP) shunt, one suffered a surgical revision of the shunt and died due to a cranial trauma unrelated to her syndrome or the previous shunt surgery, and the other did not undergo surgical revisions until the end of her follow-up. Our patients treated with endoscopic third ventriculostomy (ETV) have improved their symptomatology and have not suffered of any complications related to the hydrocephalus after the ETV surgery.
CONCLUSIONS: We update the treatment of MCAP-associated hydrocephalus and propose ETV as a valid treatment, as it seems a safe procedure with a low rate of complications.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Endoscopic third ventriculostomy (ETV); Hydrocephalus; Macrocephaly-capillary malformation (M-CM); Megalencephaly-capillary malformation (MCAP); Ventriculoperitoneal shunt (VP shunt)

Year:  2021        PMID: 34047857     DOI: 10.1007/s00381-021-05222-8

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  14 in total

1.  Macrocephaly-capillary malformation: Analysis of 13 patients and review of the diagnostic criteria.

Authors:  Víctor Martínez-Glez; Valeria Romanelli; María A Mori; Ricardo Gracia; Mabel Segovia; Antonio González-Meneses; Juan C López-Gutierrez; Esther Gean; Loreto Martorell; Pablo Lapunzina
Journal:  Am J Med Genet A       Date:  2010-12       Impact factor: 2.802

2.  Nomenclature in macrocephaly-capillary malformation syndrome.

Authors:  Christy Collins
Journal:  Am J Med Genet A       Date:  2013-04-23       Impact factor: 2.802

3.  PIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluation.

Authors:  Kim M Keppler-Noreuil; Jonathan J Rios; Victoria E R Parker; Robert K Semple; Marjorie J Lindhurst; Julie C Sapp; Ahmad Alomari; Marybeth Ezaki; William Dobyns; Leslie G Biesecker
Journal:  Am J Med Genet A       Date:  2014-12-31       Impact factor: 2.802

4.  Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndrome.

Authors:  J Clayton-Smith; B Kerr; H Brunner; L Tranebjaerg; A Magee; R C Hennekam; R F Mueller; L Brueton; M Super; J Steen-Johnsen; D Donnai
Journal:  Clin Dysmorphol       Date:  1997-10       Impact factor: 0.816

5.  Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis.

Authors:  Ghayda M Mirzaa; Robert L Conway; Karen W Gripp; Tally Lerman-Sagie; Dawn H Siegel; Linda S deVries; Dorit Lev; Nancy Kramer; Elizabeth Hopkins; John M Graham; William B Dobyns
Journal:  Am J Med Genet A       Date:  2012-01-06       Impact factor: 2.802

6.  Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?

Authors:  Dennis Döcker; Max Schubach; Moritz Menzel; Christiane Spaich; Heinz-Dieter Gabriel; Martin Zenker; Deborah Bartholdi; Saskia Biskup
Journal:  Eur J Hum Genet       Date:  2014-06-18       Impact factor: 4.246

7.  Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromes.

Authors:  Karen W Gripp; Elizabeth Hopkins; Chana Vinkler; Dorit Lev; Gustavo Malinger; Tally Lerman-Sagie; William B Dobyns
Journal:  Am J Med Genet A       Date:  2009-05       Impact factor: 2.802

8.  Severe holocord syrinx in a child with megalencephaly-capillary malformation syndrome.

Authors:  Devorah Segal; Robert F Heary; Sanjeev Sabharwal; Maureen T Barry; Xue Ming
Journal:  J Neurosurg Pediatr       Date:  2016-04-01       Impact factor: 2.375

Review 9.  Macrocephaly-cutis marmorata telangiectatica congenita: report of six new patients and a review.

Authors:  Pablo Lapunzina; Alba Gairí; Alicia Delicado; M Angeles Mori; M Luisa de Torres; Anton Goma; Marcelo Navia; Isidora López Pajares
Journal:  Am J Med Genet A       Date:  2004-09-15       Impact factor: 2.802

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

Authors:  Alim P Mitha; Kelly J Bullivant; Julie L Lauzon; Walter J Hader
Journal:  J Neurosurg Pediatr       Date:  2009-10       Impact factor: 2.375

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