Morimoto Takayuki, Ko Sung-Chul, Shimada Keiji, Nishioka Toshikazu, Tokunaga Hidemori
Department of Neurosurgery, Nara City Hospital, Nara, Japan.
Department of Pathology, Nara City Hospital, Nara, Japan.
Surg Neurol Int. 2024 Sep 20;15:335. doi: 10.25259/SNI_487_2024. eCollection 2024.
Central giant cell granuloma (CGCG) is an uncommon, benign intraosseous lesion that most frequently occurs in the mandible and maxilla.
A 31-year-old female with a medical history of Kawasaki disease presented to our hospital complaining of a clogged right ear. Head computed tomography revealed a mass in the squamous part of the right temporal bone, with osteolytic changes and invasion of the external auditory canal, middle ear, temporomandibular joint, and mastoid air cells. Enhanced magnetic resonance imaging (MRI) showed a strong signal in the intraosseous lesion. Digital subtraction angiography revealed tumor staining from multiple feeders, including the middle meningeal, posterior deep temporal, and posterior auricular arteries. Preoperative feeder embolization using a detachable coil and Embosphere Microspheres were performed for the middle meningeal artery under general anesthesia. After the endovascular treatment, we operated on the temporal bone lesion. Postoperative enhanced MRI showed subtotal resection and residual tumor near the external auditory canal, which was left in place to prevent opening the external auditory canal. The histopathological examination showed proliferation of mononuclear cells intermingled with osteoclast-like multinucleated giant cells. A diagnosis of CGCG was made. The postoperative course was uncomplicated, and the patient was discharged on day 10 of hospitalization.
We reported a rare case of CGCG in the temporal bone, managed by endovascular therapy and surgical resection. This combination therapy resulted in subtotal resection, preserving surrounding normal structures, such as the external auditory canal and tympanic cavity.
中央巨细胞肉芽肿(CGCG)是一种罕见的良性骨内病变,最常发生于下颌骨和上颌骨。
一名有川崎病病史的31岁女性因右耳堵塞前来我院就诊。头部计算机断层扫描显示右侧颞骨鳞部有一肿块,伴有骨质溶解改变,并侵犯外耳道、中耳、颞下颌关节和乳突气房。增强磁共振成像(MRI)显示骨内病变呈强信号。数字减影血管造影显示来自多个供血动脉的肿瘤染色,包括脑膜中动脉、颞深后动脉和耳后动脉。在全身麻醉下,使用可脱性弹簧圈和Embosphere微球对脑膜中动脉进行术前供血动脉栓塞。血管内治疗后,我们对颞骨病变进行了手术。术后增强MRI显示次全切除,外耳道附近残留肿瘤,为防止打开外耳道而予以保留。组织病理学检查显示单核细胞增生并夹杂破骨细胞样多核巨细胞。诊断为CGCG。术后病程顺利,患者于住院第10天出院。
我们报告了一例罕见的颞骨CGCG病例,采用血管内治疗和手术切除进行处理。这种联合治疗实现了次全切除,保留了周围正常结构,如外耳道和鼓室。