Abstract
Abstract 1085: Vagal Nerve Schwannoma Presenting As A Syncope In A Young Patient
Arteriosclerosis, thrombosis, and vascular biology, Vol.44(Suppl_1), pp.A1085-A1085
05/2024
DOI: 10.1161/atvb.44.suppl_1.1085
Abstract
Abstract only
Introduction:
Vagal schwannomas are rare, benign masses that usually develop in the cervical region but can arise anywhere along the vagus nerve. Patients may be asymptomatic; however, in most cases, patients present in their third to sixth decades, with neck swelling, hoarseness or cough. Herein, we discuss a case report of a 26-year-old male who presented after an abrupt syncopal episode with sinus bradycardia and was diagnosed with vagal schwannoma.
Case Presentation:
A 26-year-old male with a past medical history of bipolar disorder was brought to the hospital after an abrupt syncopal episode while driving. He denied any palpitations or prodromal symptoms prior to loss of consciousness. Inpatient cardiac monitoring revealed persistent sinus bradycardia, without high degree AV block. Treadmill EKG stress test confirmed chronotropic competence. CT head did not reveal other etiology of syncope. CT chest revealed a 2.4 x 2.0 cm left superior mediastinal mass. Cardiothoracic surgery was consulted for concern of thoracic outlet mass/mediastinal mass. Robotic-assisted left thoracoscopy was performed for mediastinal mass excision, which revealed a left vagus nerve schwannoma on frozen section.
Discussion:
Most vagus nerve schwannomas have been found to arise within the cervical course of the vagus nerve. Intrathoracic vagal schwannomas are rare. These tumors are usually asymptomatic, however varied symptoms such as pain, dysphagia and shortness of breath have been reported. In this case presented, the tumor possibly contributed to the heightened vagal tone and neurogenic syncope (with vasovagal syncope). It is also notable that our patient's resting heart rate normalized following excision of the mass. Of note, with a high reported incidence of peri-perioperative vocal cord paralysis, surgical excision remains a challenging mainstay of treatment in symptomatic patients.
Conclusion:
Vagal neoplasms should be hence considered as a differential diagnosis in patients with otherwise unexplained bradycardia with history of syncope.
Reference:
Neurocardiogenic syncope; Carol Chen-Scarabelli, cardiovascular nurse practitioner and Tiziano M Scarabelli, associate professor of internal medicine. BMJ 2004 Aug 7; 329 (7461):336-341.
Details
- Title: Subtitle
- Abstract 1085: Vagal Nerve Schwannoma Presenting As A Syncope In A Young Patient
- Creators
- Afsha Aurshina - United Health ServicesZainab Imtiaz - United Health ServicesVarun Rajagopalan - United Health ServicesPriyanka Singh - United Health ServicesMuhammad S Khan - United Health ServicesMichail Vitellas - United Health ServicesMuhammad Nadeem - United Health Services
- Resource Type
- Abstract
- Publication Details
- Arteriosclerosis, thrombosis, and vascular biology, Vol.44(Suppl_1), pp.A1085-A1085
- DOI
- 10.1161/atvb.44.suppl_1.1085
- ISSN
- 1079-5642
- eISSN
- 1524-4636
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
- Language
- English
- Date published
- 05/2024
- Academic Unit
- Internal Medicine; Hospital Medicine
- Record Identifier
- 9984946622402771
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