A Case of Severe Dysphagia Suspected to Result from Acute Oropharyngeal Palsy in which Balloon Dilation was Effective

Acute oropharyngeal palsy is a rare subtype of Guillain-Barré syndrome. It is characterized by dysphagia and diminished deep tendon reflexes, while notably sparing limb muscle weakness and orbicularis oculi paralysis. Due to its rarity, dysphagia caused by acute oropharyngeal palsy may remain undiagnosed. We report a case of dysphagia that developed following diabetic ketoacidosis. The patient was a man in his 70s who was transported to our hospital by emergency services due to diabetic ketoacidosis. Severe dysphagia persisted despite the successful management of his diabetic ketoacidosis. Although the diagnosis was challenging, we established a diagnosis of acute oropharyngeal palsy based on physical examination findings and cerebrospinal fluid analysis results. We observed improvement in dysphagia caused by acute oropharyngeal palsy following balloon dilation therapy. We present this case to emphasize the importance of including acute oropharyngeal palsy in the differential diagnosis when evaluating patients with bulbar palsy.

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Publication Details

Journal
The Japanese Journal of Rehabilitation Medicine
Published
2025-11-27
DOI
https://doi.org/10.2490/jjrmc.25019
Primary Topic
Neurological and metabolic disorders
Type
article
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article

A Case of Severe Dysphagia Suspected to Result from Acute Oropharyngeal Palsy in which Balloon Dilation was Effective

Masamune Ebara, Yosuke Tomiyama, T. Ito, Dai Fujiwara et al.
The Japanese Journal of Rehabilitation Medicine
Neurological and metabolic disorders
article

A Case of Severe Dysphagia Suspected to Result from Acute Oropharyngeal Palsy in which Balloon Dilation was Effective

Masamune Ebara, Yosuke Tomiyama, T. Ito, Dai Fujiwara, Ran Kiguchi
article en

Abstract

Acute oropharyngeal palsy is a rare subtype of Guillain-Barré syndrome. It is characterized by dysphagia and diminished deep tendon reflexes, while notably sparing limb muscle weakness and orbicularis oculi paralysis. Due to its rarity, dysphagia caused by acute oropharyngeal palsy may remain undiagnosed. We report a case of dysphagia that developed following diabetic ketoacidosis. The patient was a man in his 70s who was transported to our hospital by emergency services due to diabetic ketoacidosis. Severe dysphagia persisted despite the successful management of his diabetic ketoacidosis. Although the diagnosis was challenging, we established a diagnosis of acute oropharyngeal palsy based on physical examination findings and cerebrospinal fluid analysis results. We observed improvement in dysphagia caused by acute oropharyngeal palsy following balloon dilation therapy. We present this case to emphasize the importance of including acute oropharyngeal palsy in the differential diagnosis when evaluating patients with bulbar palsy.

The Japanese Journal of Rehabilitation MedicineVol. 62(12)
Tohoku University (JP), Kensei Hospital (JP)
Openalex Percentile: Top 51%
Neurological and metabolic disorders
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