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J Cancer Res Ther ; 10(2): 377-80, 2014.
Article in English | MEDLINE | ID: mdl-25022398

ABSTRACT

Primary Ewing's sarcoma (EWS) of the cranium is extremely rare. It accounts for <1% of cases. We retrospectively analyzed our EWS cases to determine those which had a primary cranial involvement. Out of a total of 332 cases of EWS registered between the years 2000 and 2011, 7 were of the primary cranial involvement. Treatment modalities included surgery, chemotherapy, and radiotherapy (RT), as indicated. The follow-up ranged from 8 months to 7.5 years. In our study, parieto-occipital region was the commonest site. Most patients presented with localized disease and swelling of the scalp. Excision followed by chemotherapy or RT appears to have good survival rates. At a median follow-up of 32.2 months, only one patient had a recurrence, and was successfully salvaged with second line chemotherapy. These cases illustrate that a multi-disciplinary approach in patients with EWS of the cranium results in a good outcome.


Subject(s)
Sarcoma, Ewing/diagnostic imaging , Skull Neoplasms/diagnostic imaging , Adolescent , Child , Child, Preschool , Combined Modality Therapy , Fatal Outcome , Female , Humans , Infant , Male , Radiography , Sarcoma, Ewing/pathology , Sarcoma, Ewing/therapy , Skull Neoplasms/pathology , Skull Neoplasms/therapy
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