颞骨中央巨细胞肉芽肿的联合血管内治疗和手术:病例报告。

Surgical neurology international Pub Date : 2024-09-20 eCollection Date: 2024-01-01 DOI:10.25259/SNI_487_2024
Takayuki Morimoto, Sung-Chul Ko, Keiji Shimada, Toshikazu Nishioka, Hidemori Tokunaga
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摘要

背景:中央巨细胞肉芽肿(CGCG中央巨细胞肉芽肿(CGCG)是一种不常见的骨内良性病变,最常发生在下颌骨和上颌骨:一名有川崎病病史的 31 岁女性来我院就诊,主诉右耳堵塞。头部计算机断层扫描显示,右颞骨鳞状部位有肿块,并伴有溶骨性改变,外耳道、中耳、颞下颌关节和乳突气室均受侵犯。增强磁共振成像(MRI)显示骨内病变处有强信号。数字减影血管造影术显示,包括脑膜中动脉、颞后深动脉和耳后动脉在内的多条供血动脉均有肿瘤染色。术前,我们在全身麻醉下使用可拆卸线圈和Embosphere微球对脑膜中动脉进行了馈源栓塞。血管内治疗后,我们对颞骨病变进行了手术。术后增强磁共振成像显示肿瘤次全切除,外耳道附近有残留肿瘤,为防止打开外耳道,我们将肿瘤留在原位。组织病理学检查显示,单核细胞与破骨细胞样多核巨细胞混杂增生。诊断结果为 CGCG。术后过程并不复杂,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,该病例通过血管内治疗和手术切除得到了控制。结论:我们报告了一例罕见的颞骨CGCG病例,该病例通过血管内治疗和手术切除进行了处理,这种综合疗法实现了次全切除,保留了周围的正常结构,如外耳道和鼓室。
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Combined endovascular therapy and surgery for central giant cell granuloma in the temporal bone: A case report.

Background: Central giant cell granuloma (CGCG) is an uncommon, benign intraosseous lesion that most frequently occurs in the mandible and maxilla.

Case description: 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.

Conclusion: 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.

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