CASE REPORT |
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Year : 2008 | Volume
: 45
| Issue : 3 | Page : 123-125 |
Leiomyosarcoma of the maxilla as second malignancy in retinoblastoma
SS Qureshi1, RC Mistry1, G Natrajan1, S Gujral2, S Laskar3, S Banavali3
1 Department of Surgical Oncology, Tata Memorial Hospital, Ernest Borges Road, Parel, Bombay, India 2 Department of Pathology, Tata Memorial Hospital, Ernest Borges Road, Parel, Bombay, India 3 Department of Pediatric Oncology, Tata Memorial Hospital, Ernest Borges Road, Parel, Bombay, India
Correspondence Address:
S S Qureshi Department of Surgical Oncology, Tata Memorial Hospital, Ernest Borges Road, Parel, Bombay India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0019-509X.44069
Patients with hereditary retinoblastoma are at increased risk of second primary tumor, the commonest tumor being osteosarcoma. Leiomyosarcoma developing as second primary neoplasm in retinoblastoma patients is unusual and most have occurred in the field of previous radiotherapy. Although with aggressive therapy better survival can be achieved, the overall prognosis of patients developing these second neoplasms is poor. In this report we present a case of leiomyosarcoma of the maxilla as a second neoplasm in a patient with bilateral retinoblastoma which has developed outside the radiation field.
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