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Giant Calvarial Ewing's Sarcoma: A Case Report.
Sarigul, Buse; Uysal, Ece; Avci, Idris; Peker, Halil; Celik, Suat.
Afiliação
  • Sarigul B; Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey.
  • Uysal E; Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey.
  • Avci I; Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey.
  • Peker H; Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey.
  • Celik S; Department of Neurosurgery, Okmeydani Education Hospital, Istanbul, Turkey.
J Neurol Surg Rep ; 79(4): e79-e82, 2018 Oct.
Article em En | MEDLINE | ID: mdl-30302304
ABSTRACT
Ewing's sarcoma (EWS) is the second most common primary bone tumor seen in children and adolescents, first being osteosarcoma. Skull lesions are seen in 6 to 9% of cases. The tumor tends to reside most frequently on frontal and parietal bones. In the literature, majority of papers on calvarial EWS present cases with intracranial involvement; extracranial extension is reported in only eight cases. The case that we are presenting in this report is a 23-year-old male patient with multiple infiltrations in femur, costal bones, and calvarium which had been diagnosed radiologically and histopathologically as EWS. The calvarial metastasis had reached a very huge size with dimensions of approximately 7.5 × 7.5 × 9.5 cm and was successfully excised totally. Twelve months of follow-up revealed no recurrence in the surgical site showing that total removal of giant cranial EWS may improve morbidity of these patients.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article