Roberts D S, Faquin W C, Deschler D G
Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA 02114, USA.
B-ENT. 2011;7(4):301-3.
To report a second primary giant cell tumour (GCT) of the temporal bone and infratemporal fossa.
Medical records were analyzed in the context of the available literature.
A 30 year-old male developed a temporal bone GCT with infratemporal fossa extension 12 years after undergoing successful surgical treatment of a GCT of the femur. These tumours were histologically distinct, suggesting the development of a second primary GCT rather than metastatic disease. This case differs from prior reported cases by surgical approach. Complete removal was achieved but required resection of the zygomatic arch and dissection of all upper facial nerve branches. The patient is disease free after 3 years with acceptable functional and cosmetic results.
Complete resection of GCTs of the temporal bone and infratemporal fossa is advocated. Surgical techniques that allow for visualization of the facial nerve and increase surgical access can enhance overall clinical success.
报告一例颞骨和颞下窝的第二原发性骨巨细胞瘤(GCT)。
结合现有文献对病历进行分析。
一名30岁男性在成功接受股骨骨巨细胞瘤手术治疗12年后,出现了累及颞下窝的颞骨骨巨细胞瘤。这些肿瘤在组织学上不同,提示为第二原发性骨巨细胞瘤而非转移性疾病。该病例与先前报道的病例在手术方式上有所不同。实现了完整切除,但需要切除颧弓并解剖所有面神经上支。患者术后3年无疾病,功能和美容效果可接受。
主张对颞骨和颞下窝的骨巨细胞瘤进行完整切除。能够可视化面神经并增加手术入路的手术技术可提高总体临床成功率。