A Case of Jugulotympanicum Paraganglioma: A Treatment Dilemma

IF 0.2 Q4 OTORHINOLARYNGOLOGY
Nurul Najwa Mohd Zakir, Izny Hafiz Zainon, Nik Adilah Nik Othman
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Abstract

Temporal bone paragangliomas arise from the paraganglion cells that are located in the middle ear and the lateral skull base. We present a 46-year-old man with undisturbed right intermittent pulsatile tinnitus, ear fullness, and progressively reduced hearing for 1 year. Clinically, the right tympanic membrane is bulging, and there is a pulsatile reddish mass in the middle ear. Computed tomography reveals soft tissue at the right mastoid air cell that extends inferiorly to the jugular foramen and laterally to the ear canal. The mass has an epicenter at the right jugular fossa and is obliterating the internal auditory meatus in magnetic resonance imaging. The diagnosis of advanced right nonsecreting jugulotympanicum paraganglioma Glasscock-Jackson type IV was established from imaging and a normal 24-h urine metanephrine level result. After extensive multidisciplinary deliberations, radiation treatment was determined to be the patient’s best course of treatment.
颈鼓室副神经节瘤1例:治疗困境
颞骨副神经节瘤起源于位于中耳和侧颅底的副神经节细胞。我们报告一位46岁的男性,患有未受干扰的右侧间歇性搏动性耳鸣,耳朵充盈,听力逐渐下降1年。临床表现:右鼓膜膨出,中耳有搏动性红色肿块。计算机断层扫描显示右侧乳突气细胞处有软组织,向下延伸至颈静脉孔,向外侧延伸至耳道。磁共振成像显示,肿块震中位于右侧颈静脉窝,掩盖了内耳道。晚期右侧非分泌性颈鼓室副神经节瘤Glasscock-Jackson IV型通过影像学检查和24小时尿肾上腺素水平正常诊断。经过广泛的多学科讨论,放射治疗被确定为患者的最佳治疗方案。
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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来源期刊
Indian Journal of Otology
Indian Journal of Otology OTORHINOLARYNGOLOGY-
CiteScore
0.40
自引率
0.00%
发文量
21
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