BPG is committed to discovery and dissemination of knowledge
Case Report
Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Clin Cases. May 6, 2026; 14(13): 117852
Published online May 6, 2026. doi: 10.12998/wjcc.v14.i13.117852
Atypical jugulotympanic paraganglioma presentation, diagnostic challenges, and role of imaging: A case report
Harshil Patel, Yonnah Okuna, Whinsky Ujima
Harshil Patel, Whinsky Ujima, Department of Medical Physiology, University of Nairobi, Nairobi 00100, Kenya
Yonnah Okuna, Department of Neurosurgery, University of Nairobi, Nairobi 00100, Kenya
Author contributions: Patel H, Okuna Y, and Ujima W contributed to manuscript writing and editing, and data collection; all authors have read and approved the final manuscript.
Informed consent statement: Written informed consent was obtained from the patient for publication of this case report and any accompanying images.
Conflict-of-interest statement: All authors declare that they have no conflict of interest to disclose.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Corresponding author: Harshil Patel, MD, Department of Medical Physiology, University of Nairobi, Upper Hill, Nairobi 00100, Kenya. harshilpatel@students.uonbi.ac.ke
Received: January 4, 2026
Revised: February 14, 2026
Accepted: March 25, 2026
Published online: May 6, 2026
Processing time: 127 Days and 1.7 Hours
Abstract
BACKGROUND

Jugular paragangliomas (JPGLs) are rare, slow-growing neuroendocrine tumors originating from the adventitia of the vessels in the jugular foramen. They typically present with pulsatile tinnitus, conductive hearing loss, and lower cranial nerve palsies. However, atypical presentations can delay diagnosis, especially in resource-limited settings.

CASE SUMMARY

We report the case of a 76-year-old woman with a long-standing history of right-sided hearing loss, intermittent chronic painless ear discharge, and lower motor facial nerve palsy, who presented with acute mastoid pain and otorrhea. Her symptoms were initially attributed to malignant otitis externa, given her diabetic status and history of a canal wall-up mastoidectomy. However, further evaluation with high-resolution computed tomography and contrast-enhanced magnetic resonance imaging (MRI) revealed an expansile lesion involving the middle ear and temporal lobe, consistent with a JPGL. Notably, she lacked pulsatile tinnitus and jugular foramen syndrome, leading to a delay in appropriate imaging and diagnosis.

CONCLUSION

This case underscores the importance of maintaining a broad differential diagnosis in patients with atypical or progressive otologic symptoms, especially when cranial neuropathies are absent. Early use of contrast-enhanced MRI is essential for detecting retrocochlear and vascular tumors in patients with atypical presentations. Clinician awareness and adherence to imaging guidelines can prevent delayed diagnosis and optimize outcomes in patients with paragangliomas.

Keywords: Neurology; Neurosurgery; Paraganglioma; Delayed diagnosis; Contrast-enhanced magnetic resonance imaging; Glomus jugulare tumor; Case report

Core Tip: Jugular paragangliomas are rare skull base tumors that typically present with pulsatile tinnitus and lower cranial nerve palsies. This case highlights an atypical presentation marked by non-pulsatile tinnitus, sensorineural hearing loss, and isolated facial nerve involvement, leading to delayed diagnosis and intracranial extension. The report emphasizes the limitations of symptom-based diagnosis and underscores the critical role of early contrast-enhanced magnetic resonance imaging in patients with unilateral, progressive otologic symptoms to enable timely diagnosis and improved clinical outcomes.