Thyroid Storm Presenting with Isolated Acute Bulbar Myopathy: A Case Report and Literature Review

Author:

AlNeyadi Asma1,AlKhanbashi Manal1,AlKaabi Fatima2,Ismail Mohamed2

Affiliation:

1. Internal Medicine Department, Tawam Hospital, Al Ain, United Arab Emirates

2. Department of Endocrinology, Tawam Hospital, Al Ain, United Arab Emirates

Abstract

AbstractWhile proximal skeletal muscle myopathy is a frequently reported complication of thyrotoxicosis, acute bulbar thyrotoxic myopathy is rare especially in absence of other forms of myopathy. In this report, we present a case of 31 years old male presenting with thyrotoxicosis and aspiration pneumonia following weeks of experiencing dysphagia and hoarseness of voice. Labs confirmed Graves' disease and other causes of bulbar myopathy like Myasthenia gravis was ruled out. He was started on thyroid treatment and showed remarkable improvement of dysphagia over 15 days. Based on this, we conclude that isolated bulbar myopathy in hyperthyroidism should be considered in patients presenting with dysphagia and dysphonia in absence of other possible neurological causes.

Publisher

Georg Thieme Verlag KG

Reference8 articles.

1. Acute bulbar muscle dysfunction and hyperthyroidism. A study of four cases and review of the literature;G M Kammer;Am J Med,1974

2. Thyrotoxic muscle disease;I Ramsay;Postgrad Med J,1968

3. Thyrotoxic myopathy. Pathomorphological observations of human material and experimentally induced thyrotoxicosis in rats;A Korényi-Both;Acta Neuropathol,1981

4. Hyperthyroidism presenting as dysphagia;H Noto;Intern Med,2000

5. Thyrotoxicosis presenting as acute bulbar palsy;B Mathew;J Assoc Physicians India,2011

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