Unmasking Villaret's syndrome: a diagnostic challenge of glomus jugulare mimicking mastoiditis.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Annals of Medicine and Surgery Pub Date : 2025-01-21 eCollection Date: 2025-02-01 DOI:10.1097/MS9.0000000000002911
Abhishek Kumar Shah, Prince Barnawal, Aayushma Kafle, Bikram Prasad Gajurel
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Abstract

Introduction: Villaret's syndrome involves unilateral palsy of cranial nerves IX to XII, often with Horner's sign, commonly caused by benign neoplasms or vascular issues. This report highlights glomus jugulare-induced Villaret syndrome, stressing careful evaluation for persistent otologic symptoms.

Case presentation: A 43-year-old woman with a history of chronic suppurative otitis media (CSOM) presented with recurrent ear discharge, pain, and severe mixed hearing loss. Despite a left tympanoplasty, symptoms persisted, leading to a canal wall down mastoidectomy. Six months later, she developed facial numbness, hoarseness, and dysphagia. Physical exam showed unilateral cranial nerve palsies with Horner's syndrome, consistent with Villaret's syndrome. Imaging confirmed a glomus jugulare tumor. After digital subtraction angiography and balloon occlusion test, surgical resection was performed. Postoperatively, she showed gradual cranial nerve recovery and remains under follow-up.

Discussion: Jugular foramen syndrome involves unilateral cranial nerve palsies, including Villaret's syndrome, where cranial nerves IX-XII and cervical sympathetic fibers are affected. Most often linked to benign neoplasms like paragangliomas, glomus jugulare tumors are slow-growing, often benign, and predominantly affect middle-aged females. Diagnosis relies on MRI's "salt-and-pepper" imaging, with high-resolution CT for bony involvement. Treatment, including surgery with embolization, aims to reduce cranial nerve deficits. Radiotherapy and radiosurgery are options for non-surgical candidates or recurrence cases.

Conclusion: This case underscores the diagnostic challenges of Villaret's syndrome caused by glomus jugulare. Initially masked by symptoms of chronic otitis media and mastoiditis, cranial nerve deficits eventually revealed the underlying tumor, highlighting the importance of vigilant assessment and imaging in persistent otologic cases.

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揭露维拉雷特综合征:模拟乳突炎的颈静脉球的诊断挑战。
简介:Villaret综合征包括脑神经IX至XII的单侧麻痹,常伴有霍纳征,通常由良性肿瘤或血管问题引起。本报告强调颈静脉球囊引起的Villaret综合征,强调仔细评估持续性耳科症状。病例介绍:一名43岁女性,有慢性化脓性中耳炎(CSOM)病史,表现为反复耳漏,疼痛和严重的混合性听力损失。尽管左鼓室成形术,症状持续,导致管壁乳突切除术。6个月后,患者出现面部麻木、声音嘶哑和吞咽困难。体检显示单侧脑神经麻痹伴有霍纳综合征,与维拉雷特综合征相符。影像学证实为颈静脉球瘤。经数字减影血管造影及球囊闭塞试验后,行手术切除。术后颅神经逐渐恢复,仍在随访中。讨论:颈静脉孔综合征涉及单侧脑神经麻痹,包括Villaret综合征,其中颅神经IX-XII和颈交感神经纤维受到影响。颈静脉球瘤通常与副神经节瘤等良性肿瘤有关,生长缓慢,通常为良性,主要影响中年女性。诊断依赖于MRI的“盐和胡椒”成像,以及骨骼受累的高分辨率CT。治疗,包括栓塞手术,旨在减少颅神经缺损。放疗和放射外科是非手术候选人或复发病例的选择。结论:本病例强调了颈静脉球囊引起的Villaret综合征的诊断挑战。颅神经缺损最初被慢性中耳炎和乳突炎的症状所掩盖,最终揭示了潜在的肿瘤,强调了在持续性耳科病例中警惕评估和影像学的重要性。
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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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