Qureshi Ss, Mistry Rc, Natrajan G, Gujral S, Laskar S, Banavali S
Department of Surgical Oncology, Tata Memorial Hospital, Ernest Borges Road, Parel, Bombay, India.
Indian J Cancer. 2008 Jul-Sep;45(3):123-5. 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.
患有遗传性视网膜母细胞瘤的患者发生第二原发性肿瘤的风险增加,最常见的肿瘤是骨肉瘤。视网膜母细胞瘤患者发生平滑肌肉瘤作为第二原发性肿瘤并不常见,且大多数发生在既往放疗区域。尽管积极治疗可提高生存率,但发生这些第二原发性肿瘤的患者总体预后较差。在本报告中,我们介绍了一例双侧视网膜母细胞瘤患者发生上颌平滑肌肉瘤作为第二原发性肿瘤,且该肿瘤发生在放疗区域之外。