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G Chir ; 28(10): 367-70, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17915050

ABSTRACT

Desmoplastic small round cell tumor (DSRCT) is a rare, highly aggressive malignancy with distinctive histological and immunohistochemical features occurring in young population with male predominance. We report a case of DRSCT occurred in a 17 years old patient which presented with a large upper left quadrant abdominal mass that was treated with a very aggressive surgical approach and multi-agent chemotherapy. At a 12 months follow-up he is free of recurrence. This kind of tumour has a very poor prognosis. No standard treatment protocol has been established. Aggressive surgery combined with postoperative multi-agent adjuvant chemotherapy is justified not only to relieve symptoms but also to try to improve the outcome.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Fibromatosis, Aggressive/drug therapy , Fibromatosis, Aggressive/surgery , Retroperitoneal Neoplasms/drug therapy , Retroperitoneal Neoplasms/surgery , Adolescent , Carcinoma, Small Cell/drug therapy , Carcinoma, Small Cell/surgery , Chemotherapy, Adjuvant , Dactinomycin/administration & dosage , Doxorubicin/administration & dosage , Fibromatosis, Aggressive/diagnostic imaging , Humans , Ifosfamide/administration & dosage , Male , Retroperitoneal Neoplasms/diagnostic imaging , Tomography, X-Ray Computed , Treatment Outcome , Vincristine/administration & dosage
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