Literature DB >> 23953647

Goldenhar syndrome and medulloblastoma: a coincidental association? The first case report.

Dror Aizenbud1, Natasha V Shoham2, Shlomi Constantini3, Neta Nevo4, Myriam Ben Arush4, Michal Raz5, Adi Rachmiel6, Dorit Goldsher7.   

Abstract

BACKGROUND: Features of Goldenhar syndrome include several craniofacial anomalies of structures derived from the first and second pharyngeal arches, as well as vertebral, cardiac and renal systems abnormalities. In addition, Goldenhar patients were reported to manifest a variety of central nervous system anomalies and several types of neoplasias. CASE HISTORY AND DISCUSSION: The first case of medulloblastoma in a patient with Goldenhar syndrome is presented here. There is no clear association between these two pathologies. We speculate that aberrant events during the migration of neural crest cells in early stages of development could be the basis of an association between medulloblastoma and Goldenhar syndrome. The case history suggests other possible etiological contributing factors to the development of medulloblastoma, such as patient's history of trauma and/or early childhood exposure to ionizing radiation.
Copyright © 2013 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Goldenhar syndrome; Medulloblastoma; Neurocristopathies; Radiation exposure; Trauma

Mesh:

Year:  2013        PMID: 23953647     DOI: 10.1016/j.jcms.2013.07.003

Source DB:  PubMed          Journal:  J Craniomaxillofac Surg        ISSN: 1010-5182            Impact factor:   2.078


  1 in total

1.  OTX2 duplication is implicated in hemifacial microsomia.

Authors:  Dina Zielinski; Barak Markus; Mona Sheikh; Melissa Gymrek; Clement Chu; Marta Zaks; Balaji Srinivasan; Jodi D Hoffman; Dror Aizenbud; Yaniv Erlich
Journal:  PLoS One       Date:  2014-05-09       Impact factor: 3.240

  1 in total

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