Kaya İsa, Benzer Murat, Turhal Göksel, Sercan Gode, Bilgen Cem, Kirazlı Tayfun
Department of Otolaryngology, Ege University School of Medicine, Izmir, Turkey.
Clinic of Otolaryngology, Selcuk State Hospital, Izmir, Turkey.
J Int Adv Otol. 2018 Apr;14(1):151-154. doi: 10.5152/iao.2018.3609.
Giant cell tumor (GCT) is a benign tumor that originates from undifferentiated mesenchymal cells of the bone marrow. The cranium as well as temporal bone is a rare location for GCTs. Despite its benign nature, GCT may be locally aggressive and has the potential to recur locally. Furthermore, GCT may give rise to pulmonary metastases (~1%) in addition to causing local bone destruction. Surgical excision is the treatment of choice for patients with GCT. We describe the case of a 56-year-old female who presented with headache and hearing loss with extensive GCT, which originated in the squamous part of the temporal bone and extended into the left mandibular fossa and middle ear. She was treated by total resection of the tumor using left temporal craniotomy approach. In this article, we present a case of temporal bone GCT with its clinical features as well as a review of the related literature.
骨巨细胞瘤(GCT)是一种起源于骨髓未分化间充质细胞的良性肿瘤。颅骨以及颞骨是GCT的罕见发病部位。尽管其本质为良性,但GCT可能具有局部侵袭性且有局部复发的可能。此外,GCT除了会导致局部骨质破坏外,还可能引发肺转移(约1%)。手术切除是GCT患者的首选治疗方法。我们描述了一例56岁女性患者,她因广泛的GCT出现头痛和听力丧失,该肿瘤起源于颞骨鳞状部并延伸至左下颌窝和中耳。她接受了采用左颞开颅手术入路的肿瘤全切除术。在本文中,我们呈现了一例颞骨GCT病例及其临床特征,并对相关文献进行了综述。