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Thyrotoxic periodic paralysis: A case report

Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by episodes of muscle weakness and hypokalemia. TPP is typically present in young Asian men, female, and non-Asian ethnic group can also be affected. TPP is a curable cause of hypokalemic periodic paralysis,...

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Detalles Bibliográficos
Autores principales: Al Moteri, Barakat Lafi G., Aslam, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Qassim Uninversity 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327672/
https://www.ncbi.nlm.nih.gov/pubmed/28293157
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author Al Moteri, Barakat Lafi G.
Aslam, Mohammad
author_facet Al Moteri, Barakat Lafi G.
Aslam, Mohammad
author_sort Al Moteri, Barakat Lafi G.
collection PubMed
description Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by episodes of muscle weakness and hypokalemia. TPP is typically present in young Asian men, female, and non-Asian ethnic group can also be affected. TPP is a curable cause of hypokalemic periodic paralysis, can often be the first manifestation of thyrotoxicosis. Factors such as high carbohydrate diet, strenuous exercise, emotional stress, and steroid can precipitate an attack of TPP. The presence of both hypokalemia and elevated level of thyroxine (T(4)) and triiodothyronine (T(3)) are important diagnostic features during the acute episode. Treatment of TPP involves two steps, immediate action to reverse the paralysis by correction of hypokalemia followed by measures to prevent future attacks by restoration of a euthyroid state. We report a first case of TPP, which was delayed to diagnose, from our hospital due to Graves’ disease in Asian man who present with second episode of paralytic attack before the diagnosis was made which is also unusual as attacks were not frequent.
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spelling pubmed-53276722017-03-14 Thyrotoxic periodic paralysis: A case report Al Moteri, Barakat Lafi G. Aslam, Mohammad Int J Health Sci (Qassim) Case Report Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by episodes of muscle weakness and hypokalemia. TPP is typically present in young Asian men, female, and non-Asian ethnic group can also be affected. TPP is a curable cause of hypokalemic periodic paralysis, can often be the first manifestation of thyrotoxicosis. Factors such as high carbohydrate diet, strenuous exercise, emotional stress, and steroid can precipitate an attack of TPP. The presence of both hypokalemia and elevated level of thyroxine (T(4)) and triiodothyronine (T(3)) are important diagnostic features during the acute episode. Treatment of TPP involves two steps, immediate action to reverse the paralysis by correction of hypokalemia followed by measures to prevent future attacks by restoration of a euthyroid state. We report a first case of TPP, which was delayed to diagnose, from our hospital due to Graves’ disease in Asian man who present with second episode of paralytic attack before the diagnosis was made which is also unusual as attacks were not frequent. Qassim Uninversity 2017 /pmc/articles/PMC5327672/ /pubmed/28293157 Text en Copyright: © International Journal of Health Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al Moteri, Barakat Lafi G.
Aslam, Mohammad
Thyrotoxic periodic paralysis: A case report
title Thyrotoxic periodic paralysis: A case report
title_full Thyrotoxic periodic paralysis: A case report
title_fullStr Thyrotoxic periodic paralysis: A case report
title_full_unstemmed Thyrotoxic periodic paralysis: A case report
title_short Thyrotoxic periodic paralysis: A case report
title_sort thyrotoxic periodic paralysis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327672/
https://www.ncbi.nlm.nih.gov/pubmed/28293157
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