后窝巨大腺样囊性癌伴颅底侵犯模拟颈静脉球:1例报告及文献复习。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2023-01-01 DOI:10.1177/20363613221150218
Anand Kumar Das, Saraj Kumar Singh, Kranti Bhavana, Subhash Kumar
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引用次数: 0

摘要

作者报告一例罕见的巨大腺样囊性癌(ACC),类似于大副神经节瘤合并下颅神经麻痹。一位60岁女性,表现为耳后肿胀进行性增加,伴有单侧听力丧失、面部偏斜、吞咽困难和声音嘶哑。脑MRI显示高度血管浸润和溶骨肿块提示颈内血管球与肉瘤。它完全吞没了颈静脉孔和下颅神经颈静脉孔和枕髁的骨质侵蚀。整个乳突充满了肿瘤。数字减影血管造影显示颈外动脉枕支和椎动脉供血最多。患者接受了经皮栓塞,随后进行了颈外动脉结扎和肿块切除。术后过程平淡无奇。组织病理学提示混合性acc。病人接受放射治疗。随访1年,无复发及远处转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Posterior fossa giant adenoid cystic carcinoma with skull base invasion mimicking glomus jugulare: A case report and review of literature.

The author describes a rare case of giant adenoid cystic carcinoma (ACC) mimicking large paraganglioma with lower cranial nerve palsy. A 60-year-old female presented with a progressive increase in postauricular swelling with unilateral hearing loss, facial deviation, difficulty in swallowing, and hoarseness of voice. MRI brain showed highly vascular infiltrating and osteolytic mass suggestive of large glomus jugulare versus sarcoma. It was completely engulfing the jugular foramen and lower cranial nerves with bony erosion of the jugular foramen and occipital condyle. The whole mastoid was filled with the tumor. On digital subtraction angiography the majority of blood supply was from the occipital branch of the external carotid artery and vertebral artery. The patient underwent percutaneous embolization followed by external carotid ligation and resection of the mass. The postoperative course was uneventful. Histopathology was suggestive of mixed ACCs. The patient received radiotherapy. After 1 year of follow up no recurrence or distant metastasis was noted.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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