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      Myopathic dysphagia caused by thyrotoxicosis: a case report and review of the literature

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          Abstract

          Summary

          Myopathy caused by thyrotoxicosis is not uncommon. Skeletal muscles are commonly involved, but dysphagia is a rare manifestation of thyrotoxicosis. We aim to raise awareness of dysphagia caused by hyperthyroidism and review similar cases in the literature. We present a case of severe dysphagia caused by hyperthyroidism. We also summarize similar case reports in the literature. Our patient is a 77-year-old man who presented with thyrotoxicosis related to Graves’ disease (GD), dysphagia to both liquid and solid food, and weight loss. Further investigations revealed severe esophageal dysphagia and a high risk for aspiration. He required the placement of a G-tube for feeding. After 8 weeks of methimazole treatment, his thyroid function normalized and his dysphagia improved significantly, leading to the removal of the feeding G-tube. We summarize 19 case reports published in the literature of hyperthyroidism leading to dysphagia. Patients with thyrotoxicosis and dysphagia are at higher risk for aspiration pneumonia and thyroid storm. Based on previous case reports, on average, approximately 3 weeks of treatment with anti-thyroidal drugs and beta-blockers is needed before patients can eat normally. We report a case of dysphagia associated with GD, which is rare and needs prompt recognition to restore euthyroid status. Dysphagia generally resolved with normalization of thyroid function.

          Learning points
          • Myopathy caused by thyrotoxicosis is not uncommon.

          • Skeletal muscles are commonly involved, but dysphagia is a rare manifestation of thyrotoxicosis.

          • Dysphagia due to hyperthyroidism resolves with normalization of thyroid function.

          • Early recognition of dysphagia related to hyperthyroidism and early initiation of therapy may help reverse the dysphagia and prevent complications.

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          Most cited references14

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          Dysphagia as a manifestation of thyrotoxicosis: report of three cases and literature review.

          Myopathy is frequently associated with thyrotoxicosis. Skeletal muscles are predominantly involved in thyrotoxic myopathy, but dysphagia is extremely rare. We report three cases of thyrotoxicosis with dysphagia and review of the literature of the past 30 years. Most of these patients had antecedent muscle weakness before the onset of dysphagia although some suffered from a sudden onset of bulbar palsy. Either a myopathic or neuropathic pattern was found on electromyography. The incidence of oropharyngeal dysphagia was higher than that of esophageal motility dysfunction. Aspiration pneumonia occurred more accompanied by oropharyngeal dysphagia. The swallowing disorder could be resolved completely within 3 weeks after treatment for thyrotoxicosis. In light of these clinical experiences, early intensive treatment that includes antithyroid agent, beta-blocker, and Lugol solution may be necessary.
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            Acute bulbar muscle dysfunction and hyperthyroidism. A study of four cases and review of the literature.

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              Hyperthyroidism presenting as dysphagia.

              A 65-year-old man presented with hyperthyroidism associated with thyrotoxic dysphagia. Treatment with thiamazole improved his symptoms promptly. Although dysphagia is a rare manifestation of thyrotoxicosis, it should be emphasized that the possibility of hyperthyroidism must be discussed in unexplained dysphagia because it is readily treatable.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                27 October 2022
                2022
                : 2022
                : 21-0175
                Affiliations
                [1 ]Department of Medicine , Division of Endocrinology and Metabolism, University of Toronto, Toronto, Ontario, Canada
                [2 ]College of Medicine , King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia
                [3 ]King Abdullah International Medical Research Center , Jeddah, Saudi Arabia
                [4 ]Department of Medicine , King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Jeddah, Saudi Arabia
                [5 ]Department of Medicine , Division of Neurology, University of Toronto, Toronto, Ontario, Canada
                [6 ]Department of Laboratory Medicine and Pathobiology , University of Toronto, Toronto, Canada
                [7 ]Department of Pathology and Laboratory Medicine , Mount Sinai Hospital, Toronto, Ontario, Canada
                Author notes
                Correspondence should be addressed to R Alwithenani; Email: alwithenanira@ 123456mngha.med.sa
                Author information
                http://orcid.org/0000-0001-5660-9753
                Article
                EDM210175
                10.1530/EDM-21-0175
                9716415
                36448823
                701e2021-fabd-48f6-ad3f-13e82e396da0
                © The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License..

                History
                : 08 October 2022
                : 27 October 2022
                Categories
                Adult
                Male
                White
                Canada
                Thyroid
                Diabetes
                Unique/Unexpected Symptoms or Presentations of a Disease
                Unique/Unexpected Symptoms or Presentations of a Disease

                adult,male,white,canada,thyroid,diabetes,unique/unexpected symptoms or presentations of a disease,november,2022

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