Glossopharyngeal Neuralgia: Vagoglossopharyngeal Neuralgia

2013 ◽  
pp. 1382-1382
2021 ◽  
pp. 5-11
Author(s):  
Victor Souza ◽  
Maria Passerini ◽  
Bianca Sobral ◽  
Vinicius Baiardi ◽  
Hilton Junior

Introduction Glossopharyngeal neuralgia is a rare syndrome characterized by paroxysms of unilateral and severe stabbing pain occurring in the nerve’s distribution. Although other neuralgias are well described in the medical literature, glossopharyngeal neuralgia and its physiopathology are not. The vascular compression at the nerve root entry zone is the primary explanation for the disease. The first-line treatment is pharmacological, including carbamazepine, oxcarbazepine, and gabapentin. Surgical treatment is offered to medication-refractory patients, and microvascular decompression surgery has the best outcomes. Objective To investigate the pathophysiological and clinical aspects of the different presentations of glossopharyngeal neuralgia. Method: A systematic review of the literature including case reports and clinical trials, was done. Results A search of the literature yielded 31 papers that regarded glossopharyngeal neuralgia or its variants. Eight of these reports regarded vagoglossopharyngeal neuralgia. Seven regarded the glossopharyngeal neuralgia followed by or caused by another disease. Conclusion Glossopharyngeal neuralgia is a rare disease and requires further studies on its mechanism and clinical assessment; the physician needs to know how to distinguish it from its variants and underlying causes.


EP Europace ◽  
2003 ◽  
Vol 5 (2) ◽  
pp. 149-152 ◽  
Author(s):  
M. Ozenci ◽  
R. Karaoguz ◽  
C. Conkbayir ◽  
T. Altin ◽  
Y. Kanpolat

Abstract A glossopharyngeal neuralgia case with cardiac asystole is presented. The sinus mode dysfunction and subsequent syncope with pain appears to be the most important life-threatening symptom in the late period of the disease. Because of cardiac symptoms induced by intense vagal stimulation, this case was considered to be vagoglossopharyngeal neuralgia. Several medical and surgical alternatives have been proposed for its treatment. In the presented case the cause of disease was compression of lower cranial nerves in the right cerebello-pontine angle (CPA) by the vertebro-basilar arterial system. Carbamazepine and pacing were determined ineffective, so the patient was treated surgically by cutting the glossopharyngeal nerve and by decompression of the vagal nerve at the CPA. The sinus arrest and paroxysmal pain attacks disappeared and the patient's life returned to normal.


2014 ◽  
Vol 75 (S 02) ◽  
Author(s):  
Miguel Lopez-Gonzalez ◽  
E. Dolan

Neurosurgery ◽  
2019 ◽  
Vol 87 (5) ◽  
pp. E573-E577
Author(s):  
C Michael Honey ◽  
Marie T Krüger ◽  
Alan R Rheaume ◽  
Josue M Avecillas-Chasin ◽  
Murray D Morrison ◽  
...  

Abstract BACKGROUND AND IMPORTANCE Hemi-laryngopharyngeal spasm (HeLPS) has been recently described but is not yet widely recognized. Patients describe intermittent coughing and choking and can be cured following microvascular decompression of their Xth cranial nerve. This case report and literature review highlight that HeLPS can co-occur with glossopharyngeal neuralgia (GN) and has been previously described (but not recognized) in the neurosurgical literature. CLINICAL PRESENTATION A patient with GN and additional symptoms compatible with HeLPS is presented. The patient reported left-sided, intermittent, swallow-induced, severe electrical pain radiating from her ear to her throat (GN). She also reported intermittent severe coughing, throat contractions causing a sense of suffocation, and dysphonia (HeLPS). All her symptoms resolved following a left microvascular decompression of a loop of the posterior inferior cerebellar artery that was pulsating against both the IXth and Xth cranial nerves. A review of the senior author's database revealed another patient with this combination of symptoms. An international literature review found 27 patients have been previously described with symptoms of GN and the additional (but not recognized at the time) symptoms of HeLPS. CONCLUSION This review highlights that patients with symptoms compatible with HeLPS have been reported since 1926 in at least 4 languages. This additional evidence supports the growing recognition that HeLPS is another neurovascular compression syndrome. Patients with HeLPS continue to be misdiagnosed as conversion disorder. The increased recognition of this new medical condition will require neurosurgical treatment and should alleviate the suffering of these patients.


1982 ◽  
Vol 90 (1) ◽  
pp. 16-19 ◽  
Author(s):  
Steven M. Sobol ◽  
Benjamin G. Wood ◽  
J. Michael Conoyer

Glossopharyngeal neuralgia has been reported in association with asystole, bradycardia, and convulsions secondary to a variety of causes. Two cases of glossopharyngeal neuralgia-asystole syndrome in association with ipsilateral lesions of the parapharyngeal space are described. A pathogenetic mechanism is proposed in which parapharyngeal space lesions induce neural irritation of the glossopharyngeal afferent pain fibers and reflex afferents within the nerve of Hering to produce the syndrome. The diagnostic and therapeutic dilemmas posed by these patients are discussed.


2018 ◽  
Vol 35 (3) ◽  
pp. 395-402 ◽  
Author(s):  
Rafik Shereen ◽  
Brady Gardner ◽  
Juan Altafulla ◽  
Emily Simonds ◽  
Joe Iwanaga ◽  
...  

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