ArticleCureus2024
Thyrotoxic Periodic Paralysis: A Unique Case Highlighting the Diagnostic Challenges and Management.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Efficacy of non-invasive neuromodulation for chronic tinnitus: a systematic review and meta-analysis of randomized controlled trials.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026Review
- The Hidden Crisis: A Rare Case of Thyrotoxicosis in a Young Female, Mimicking Neuromuscular Disease.Journal of community hospital internal medicine perspectives · 2026Article
- Thyrotoxic Hypokalemic Periodic Paralysis: Pathophysiological Mechanisms.Endocrinology and metabolism (Seoul, Korea) · 2025Review
- A Trajectory of Thyroid Function: From Thyrotoxic Paralysis to Post-ablative Hypothyroidism.Cureus · 2025Article
- Article
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Authors and funding
5 authors.
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Abstract
Thyrotoxic periodic paralysis (TPP) is a rare complication primarily associated with thyrotoxicosis, particularly in individuals with Graves' disease. While more common in males aged 20 to 40, it can occur across all ethnic backgrounds. It is the most common type of acquired periodic paralysis. The condition is triggered by factors like exercise, stress, diet, and certain medications. The diagnosis is confirmed by severe hypokalemia and elevated thyroid hormones in the presence of acute flaccid paralysis. Immediate treatment involves correcting hypokalemia, while long-term management focuses on normalizing thyroid levels. In this article, we will report a case of a 30-year-old Middle Eastern man who presented to the emergency room with severe muscle weakness following extensive exertion and a high-carbohydrate diet. Physical examination revealed motor weakness in all limbs, particularly his lower limbs. Initial tests showed marked hypokalemia and biochemical thyrotoxicosis with suppressed thyroid-stimulating hormone (TSH) and elevated free triiodothyronine (T3) and free thyroxine (T4). An electrocardiogram (ECG) indicated signs of severe hypokalemia with an atrioventricular (AV) block. After he was diagnosed with TPP, the patient received oral and intravenous potassium infusions and was started on anti-thyroid medications, most importantly beta (β)-blockers. Following acute treatment, his potassium levels normalized, and he regained full muscle function. Ultimately, he was maintained on anti-thyroid medications at discharge to maintain an euthyroid state in order to prevent future recurrences of symptoms. Consequently, in patients presenting with acute flaccid paralysis, potassium level, and thyroid function should be investigated in order to promptly diagnose complications of thyrotoxicosis and to start an early appropriate combined therapy. The early and rapid management of TPP can prevent serious cardiopulmonary complications.
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