| Literature DB >> 20074817 |
Rafael Linard Avelar1, Valber Barbosa Martins, Antonio Azoubel Antunes, Patricio José de Oliveira Neto, Emanuel Sávio de Souza Andrade.
Abstract
Gorham's disease (Gorham-Stout syndrome) is a rare condition of unknown etiology involving a localized endothelial proliferation of lymph vessels resulting in destruction with bone resorption. The syndrome is rarely seen in the facial skeleton and has a large variety of prognoses and treatments. A case of this syndrome in a 9-year-old boy is presented. The clinical aspects are described, together with the treatment involving zoledronic acid. Other treatments described in the literature are reviewed. The authors believe that this report is one of the first cases in which a child afflicted in the first decade of life survives. Copyright 2009 Elsevier Ireland Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20074817 DOI: 10.1016/j.ijporl.2009.12.007
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN: 0165-5876 Impact factor: 1.675