A Case of Myopathic Dysphagia Secondary to Thyrotoxicosis
Hsieh En Chua, Lip Hong Tan, Chee Kian Chew

TL;DR
A 70-year-old man with thyrotoxicosis developed severe swallowing difficulties that improved after treating his overactive thyroid.
Contribution
This case highlights myopathic dysphagia as a rare but treatable complication of thyrotoxicosis.
Findings
The patient's dysphagia resolved with carbimazole and propranolol as thyrotoxicosis improved.
Normalization of thyroid hormone levels correlated with clinical improvement in swallowing.
Early euthyroid status is crucial to prevent aspiration and related complications.
Abstract
Myopathic dysphagia is a rare manifestation of thyrotoxicosis. Dysphagia may be isolated or may be associated with preceding proximal myopathy. We describe a 70-year-old man with newly diagnosed Graves’ disease who presented with acute dysphagia with both liquids and solids for 3 weeks, with free thyroxine >73 pmol/L (reference range 8-16 pmol/L), free triiodothyronine >40 pmol/L (reference range 3.5-6.0 pmol/L), thyroid-stimulating hormone <0.01 mIU/L (reference range 0.45-4.50 mIU/L), and thyroid-stimulating hormone receptor antibody 28.6 IU/L (reference range 0.0-1.0 IU/L). This was associated with heat intolerance, palpitations, diarrhea, proximal weakness, and weight loss. A video fluoroscopy study confirmed moderate oropharyngeal dysphagia. Evaluation was done to exclude other causes including mechanical compression, neuromuscular causes, and malignancy. The patient’s dysphagia…
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Taxonomy
TopicsThyroid Disorders and Treatments · Thyroid and Parathyroid Surgery · Dysphagia Assessment and Management
