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Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report

BACKGROUND: Immune thrombocytopenic purpura is a condition associated with an unusual, unexplained, and sometimes very severe reduction in the level of platelets in the blood. Though documented, its association with Graves’ disease is not very common and can easily be missed or misdiagnosed, leading...

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Autores principales: Agyapong, Kwabena Oteng, Folson, Aba A., Fiador, Kate, Kootin-Sanwu, Cecilia, Tufuor, Martha, Bampoh, Sally Afua, Fiscian, Henrietta, Wonkyi, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072916/
https://www.ncbi.nlm.nih.gov/pubmed/37016396
http://dx.doi.org/10.1186/s13256-023-03869-2
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author Agyapong, Kwabena Oteng
Folson, Aba A.
Fiador, Kate
Kootin-Sanwu, Cecilia
Tufuor, Martha
Bampoh, Sally Afua
Fiscian, Henrietta
Wonkyi, Roland
author_facet Agyapong, Kwabena Oteng
Folson, Aba A.
Fiador, Kate
Kootin-Sanwu, Cecilia
Tufuor, Martha
Bampoh, Sally Afua
Fiscian, Henrietta
Wonkyi, Roland
author_sort Agyapong, Kwabena Oteng
collection PubMed
description BACKGROUND: Immune thrombocytopenic purpura is a condition associated with an unusual, unexplained, and sometimes very severe reduction in the level of platelets in the blood. Though documented, its association with Graves’ disease is not very common and can easily be missed or misdiagnosed, leading to excessive bleeding and mortality. Treatment with steroids and antithyroid medications has been shown to be beneficial in correcting thrombocytopenia in these patients, although the response is varied. We report on a patient with Graves’ disease who presents with immune thrombocytopenic purpura. CASE PRESENTATION: A 37-year-old Ghanaian female presented to our hospital’s emergency department with a complaint of palpitations, difficulty breathing, easy fatigue, and headaches. She had been referred from a peripheral hospital as a case of thrombocytopenia, severe anemia, and anterior neck swelling. She was diagnosed with Graves’ disease 2 years ago, became euthyroid during treatment, but defaulted. On further examination and investigation, she was diagnosed with immune thrombocytopenic purpura and was also found to have elevated free T3 and T4, and suppressed thyroid stimulating hormone. She also had high thyroid autoantibodies. She was initially started on oral prednisolone but there was no stabilization of platelets until methimazole was introduced, which improved and normalized her platelet count. CONCLUSION: The association of Graves’ disease with immune thrombocytopenic purpura, though documented, is uncommon, and very few cases have been reported thus far. There have not been any reported cases in Ghana or Sub-Saharan Africa and hence, clinicians should be aware of this association when investigating immune thrombocytopenic purpura and should consider Graves’ disease as a possible cause. From this study, we observed that there was no improvement in platelet count following the use of corticosteroid therapy until methimazole was started.
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spelling pubmed-100729162023-04-05 Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report Agyapong, Kwabena Oteng Folson, Aba A. Fiador, Kate Kootin-Sanwu, Cecilia Tufuor, Martha Bampoh, Sally Afua Fiscian, Henrietta Wonkyi, Roland J Med Case Rep Case Report BACKGROUND: Immune thrombocytopenic purpura is a condition associated with an unusual, unexplained, and sometimes very severe reduction in the level of platelets in the blood. Though documented, its association with Graves’ disease is not very common and can easily be missed or misdiagnosed, leading to excessive bleeding and mortality. Treatment with steroids and antithyroid medications has been shown to be beneficial in correcting thrombocytopenia in these patients, although the response is varied. We report on a patient with Graves’ disease who presents with immune thrombocytopenic purpura. CASE PRESENTATION: A 37-year-old Ghanaian female presented to our hospital’s emergency department with a complaint of palpitations, difficulty breathing, easy fatigue, and headaches. She had been referred from a peripheral hospital as a case of thrombocytopenia, severe anemia, and anterior neck swelling. She was diagnosed with Graves’ disease 2 years ago, became euthyroid during treatment, but defaulted. On further examination and investigation, she was diagnosed with immune thrombocytopenic purpura and was also found to have elevated free T3 and T4, and suppressed thyroid stimulating hormone. She also had high thyroid autoantibodies. She was initially started on oral prednisolone but there was no stabilization of platelets until methimazole was introduced, which improved and normalized her platelet count. CONCLUSION: The association of Graves’ disease with immune thrombocytopenic purpura, though documented, is uncommon, and very few cases have been reported thus far. There have not been any reported cases in Ghana or Sub-Saharan Africa and hence, clinicians should be aware of this association when investigating immune thrombocytopenic purpura and should consider Graves’ disease as a possible cause. From this study, we observed that there was no improvement in platelet count following the use of corticosteroid therapy until methimazole was started. BioMed Central 2023-04-05 /pmc/articles/PMC10072916/ /pubmed/37016396 http://dx.doi.org/10.1186/s13256-023-03869-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Agyapong, Kwabena Oteng
Folson, Aba A.
Fiador, Kate
Kootin-Sanwu, Cecilia
Tufuor, Martha
Bampoh, Sally Afua
Fiscian, Henrietta
Wonkyi, Roland
Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title_full Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title_fullStr Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title_full_unstemmed Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title_short Graves’ disease-induced immune thrombocytopenic purpura in an African female: a case report
title_sort graves’ disease-induced immune thrombocytopenic purpura in an african female: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072916/
https://www.ncbi.nlm.nih.gov/pubmed/37016396
http://dx.doi.org/10.1186/s13256-023-03869-2
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