A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome

A 46-year-old female presented to the emergency room due to the chief complaint of left-sided weakness. By imaging study, she was diagnosed with cerebral infarction. Thrombolytic and antiplatelet agents were not considered due to the “golden hour” for treatment having passed and a low platelet count...

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Detalles Bibliográficos
Autores principales: Kim, Hanjun, Hwang, Sang Sun, Uh, Young, Kim, Juwon, Yoon, Kap Jun, Lee, Ji-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102048/
https://www.ncbi.nlm.nih.gov/pubmed/25035678
http://dx.doi.org/10.4274/tjh.2013.0064
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author Kim, Hanjun
Hwang, Sang Sun
Uh, Young
Kim, Juwon
Yoon, Kap Jun
Lee, Ji-Yong
author_facet Kim, Hanjun
Hwang, Sang Sun
Uh, Young
Kim, Juwon
Yoon, Kap Jun
Lee, Ji-Yong
author_sort Kim, Hanjun
collection PubMed
description A 46-year-old female presented to the emergency room due to the chief complaint of left-sided weakness. By imaging study, she was diagnosed with cerebral infarction. Thrombolytic and antiplatelet agents were not considered due to the “golden hour” for treatment having passed and a low platelet count. The peripheral blood smear, bone marrow biopsy, and aspirate findings were consistent with immune thrombocytopenic purpura. The chromosome analysis revealed the 47,XXX karyotype. To the best of our knowledge, this is the first case report associated with the comorbidities of cerebral infarction, idiopathic thrombocytopenic purpura, and triple X syndrome.
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spelling pubmed-41020482014-07-17 A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome Kim, Hanjun Hwang, Sang Sun Uh, Young Kim, Juwon Yoon, Kap Jun Lee, Ji-Yong Turk J Haematol Case Report A 46-year-old female presented to the emergency room due to the chief complaint of left-sided weakness. By imaging study, she was diagnosed with cerebral infarction. Thrombolytic and antiplatelet agents were not considered due to the “golden hour” for treatment having passed and a low platelet count. The peripheral blood smear, bone marrow biopsy, and aspirate findings were consistent with immune thrombocytopenic purpura. The chromosome analysis revealed the 47,XXX karyotype. To the best of our knowledge, this is the first case report associated with the comorbidities of cerebral infarction, idiopathic thrombocytopenic purpura, and triple X syndrome. Galenos Publishing 2014-06 2014-06-10 /pmc/articles/PMC4102048/ /pubmed/25035678 http://dx.doi.org/10.4274/tjh.2013.0064 Text en © Turkish Journal of Hematology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Hanjun
Hwang, Sang Sun
Uh, Young
Kim, Juwon
Yoon, Kap Jun
Lee, Ji-Yong
A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title_full A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title_fullStr A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title_full_unstemmed A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title_short A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome
title_sort case associated with comorbidities among cerebral infarction, idiopathic thrombocytopenic purpura, and triple x syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102048/
https://www.ncbi.nlm.nih.gov/pubmed/25035678
http://dx.doi.org/10.4274/tjh.2013.0064
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