Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke

Here we report a case of atypical thrombotic thrombocytopenic purpura that presented as an ischemic cerebrovascular accident. A 56-year-old man with multiple cardiovascular risk factors presented with sudden left-sided weakness, slurred speech, and left facial droop. He showed mild improvement when...

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Main Authors: Pradeepthi Badugu, Modupe Idowu
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2019/7425320
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spelling doaj-eb39411dd79a460aa6913e81438aa0da2020-11-25T01:37:07ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792019-01-01201910.1155/2019/74253207425320Atypical Thrombotic Thrombocytopenic Purpura Presenting as StrokePradeepthi Badugu0Modupe Idowu1Division of Hematology, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6411 Fannin Street, Houston 77030, USADivision of Hematology, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6411 Fannin Street, Houston 77030, USAHere we report a case of atypical thrombotic thrombocytopenic purpura that presented as an ischemic cerebrovascular accident. A 56-year-old man with multiple cardiovascular risk factors presented with sudden left-sided weakness, slurred speech, and left facial droop. He showed mild improvement when he was treated with thrombolytic therapy according to the hospital stroke protocol. Later in the course, he developed thrombocytopenia followed by schistocytes revealed by peripheral blood smear and other lab abnormalities. Thrombotic thrombocytopenic purpura (TTP) was suspected, and he was treated with total plasma exchange that improved his condition significantly. This case shows that TTP can have unusual and atypical presentations either with the first episode or upon relapse, making diagnosis extremely difficult. Because patients may not present the expected clinical findings, it is important to be aware of variant presentations. In the early stages of the disease, platelet aggregation and thrombus formation may not be widespread, and thrombocytopenia and microangiopathic hemolytic anemia may not be clinically evident. Patients can present soon after the onset of symptoms when the typical laboratory abnormalities may not have had ample time to manifest. Although most other similar cases in the literature had a previous typical presentation of the disease before an atypical presentation, our patient’s first presentation was atypical. An atypical presentation of disease in a patient with cardiovascular risk factors may therefore be extremely difficult to diagnose. We believe that TTP should be considered for any patient presenting with stroke and thrombocytopenia.http://dx.doi.org/10.1155/2019/7425320
collection DOAJ
language English
format Article
sources DOAJ
author Pradeepthi Badugu
Modupe Idowu
spellingShingle Pradeepthi Badugu
Modupe Idowu
Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
Case Reports in Hematology
author_facet Pradeepthi Badugu
Modupe Idowu
author_sort Pradeepthi Badugu
title Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
title_short Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
title_full Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
title_fullStr Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
title_full_unstemmed Atypical Thrombotic Thrombocytopenic Purpura Presenting as Stroke
title_sort atypical thrombotic thrombocytopenic purpura presenting as stroke
publisher Hindawi Limited
series Case Reports in Hematology
issn 2090-6560
2090-6579
publishDate 2019-01-01
description Here we report a case of atypical thrombotic thrombocytopenic purpura that presented as an ischemic cerebrovascular accident. A 56-year-old man with multiple cardiovascular risk factors presented with sudden left-sided weakness, slurred speech, and left facial droop. He showed mild improvement when he was treated with thrombolytic therapy according to the hospital stroke protocol. Later in the course, he developed thrombocytopenia followed by schistocytes revealed by peripheral blood smear and other lab abnormalities. Thrombotic thrombocytopenic purpura (TTP) was suspected, and he was treated with total plasma exchange that improved his condition significantly. This case shows that TTP can have unusual and atypical presentations either with the first episode or upon relapse, making diagnosis extremely difficult. Because patients may not present the expected clinical findings, it is important to be aware of variant presentations. In the early stages of the disease, platelet aggregation and thrombus formation may not be widespread, and thrombocytopenia and microangiopathic hemolytic anemia may not be clinically evident. Patients can present soon after the onset of symptoms when the typical laboratory abnormalities may not have had ample time to manifest. Although most other similar cases in the literature had a previous typical presentation of the disease before an atypical presentation, our patient’s first presentation was atypical. An atypical presentation of disease in a patient with cardiovascular risk factors may therefore be extremely difficult to diagnose. We believe that TTP should be considered for any patient presenting with stroke and thrombocytopenia.
url http://dx.doi.org/10.1155/2019/7425320
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