| Literature DB >> 23827687 |
Noriko Morimoto1, Hideki Ogiwara, Osamu Miyazaki, Masayuki Kitamuara, Sachiko Nishina, Atsuko Nakazawa, Takanobu Maekawa, Nobuhito Morota.
Abstract
Gorham-Stout syndrome is a rare disorder characterized by progressive osteolysis that leads to the disappearance of bone. Lymphvascular proliferation causes the local destruction of bony tissue. Owing to the low incidence of this syndrome, little is known about its etiology or treatment. We present an 11-year-old girl with Gorham-Stout syndrome that involved right petrous apex in temporal bone and upper clivus, which cause intracranial pressure increase and cerebrospinal fluid (CSF) leakage. The patient required surgical repair of CSF leakage by extradural middle fossa approach with temporal fascia flap. Combined treatment with interferon and propranolol prevented the progression of osteolysis.Entities:
Keywords: CSF leak; Interferon-α2; Lymphovascular proliferation; Petrous apex; Proplanolol; VEGF
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Year: 2013 PMID: 23827687 DOI: 10.1016/j.ijporl.2013.06.004
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN: 0165-5876 Impact factor: 1.675