Agrawal Neeraj, Chintagumpala Murali, Hicks John, Eldin Karen, Paulino Arnold C
Department of Radiation Oncology, The Methodist Hospital, Houston, TX 77030, USA.
J Pediatr Hematol Oncol. 2012 Oct;34(7):e304-7. doi: 10.1097/MPH.0b013e318266baa8.
Sinonasal teratocarcinosarcoma is an extremely rare and aggressive neoplasm with <100 cases described in the literature and only 3 reported pediatric cases. We describe a 15-year-old male with a case of sinonasal teratocarcinosarcoma with extension to the cribriform plate. He presented with epistaxis, nasal obstruction, and frontal headaches and was treated with resection and postoperative chemoradiation. He is currently doing well without evidence of recurrence 45 months after therapy.
鼻窦畸胎癌肉瘤是一种极其罕见且侵袭性强的肿瘤，文献报道不足100例，儿科病例仅有3例。我们报告一例15岁男性鼻窦畸胎癌肉瘤患者，肿瘤已累及筛板。患者表现为鼻出血、鼻塞和前额头痛，接受了手术切除及术后放化疗。治疗后45个月，患者目前情况良好，无复发迹象。
