Poster 323 Glossopharyngeal Neuralgia Presenting as Neck Pain: A Case Report

PM&R ◽  
2011 ◽  
Vol 3 ◽  
pp. S284-S285
Author(s):  
Berdale S. Colorado ◽  
Matthew P. West
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.


PM&R ◽  
2016 ◽  
Vol 8 (9) ◽  
pp. S303-S304
Author(s):  
Annie R. Layno-Moses ◽  
Tariq Malik ◽  
Joshua J. Minori

2020 ◽  
Vol 7 (3) ◽  
pp. 117-120
Author(s):  
Forhad H Chowdhury ◽  
Jalal Uddin Mohammod Rumi ◽  
Farhanaz Zainab ◽  
Maliha Hakim

2012 ◽  
Vol 81 (2) ◽  
pp. 93-97
Author(s):  
S. A. E. Van Meervenne ◽  
J. Declercq ◽  
A. Tipold ◽  
K. Chiers ◽  
I. Van Soens ◽  
...  

Acute steroid responsive meningitis-arteritis (SRMA) is a common neurological disorder in young dogs. Typical clinical symptoms of the acute form of SRMA are neck pain, depression and fever. This case report describes a 1.5-year-old Pointer with uncommon neurological deficits (unilateral multiple cranial nerve deficits and Horner’s syndrome) and an exceptional necrosis of the tongue. This was believed to be part of the systemic vasculitis accompanying SRMA. The patient also developed tail necrosis and iatrogenic calcinosis cutis, which complicated further treatment of the dog.


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