Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura

Background: Thrombotic thrombocytopenic purpura (TTP) is a hematological emergency requiring prompt plasmapheresis. Conversely, vitamin B12 deficiency is a relatively benign diagnosis that can mimic microangiopathic hemolytic anemia, characterized by the presence of anemia, thrombocytopenia, indirec...

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Main Authors: Pegah Jahangiri, Rachel Hicks, Prabjot K. Batth, Christopher J. Haas
Format: Article
Language:English
Published: Greater Baltimore Medical Center 2021-05-01
Series:Journal of Community Hospital Internal Medicine Perspectives
Subjects:
Online Access:http://dx.doi.org/10.1080/20009666.2021.1893143
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author Pegah Jahangiri
Rachel Hicks
Prabjot K. Batth
Christopher J. Haas
author_facet Pegah Jahangiri
Rachel Hicks
Prabjot K. Batth
Christopher J. Haas
author_sort Pegah Jahangiri
collection DOAJ
description Background: Thrombotic thrombocytopenic purpura (TTP) is a hematological emergency requiring prompt plasmapheresis. Conversely, vitamin B12 deficiency is a relatively benign diagnosis that can mimic microangiopathic hemolytic anemia, characterized by the presence of anemia, thrombocytopenia, indirect hyperbilirubinemia, markers of hemolysis, and schistocytes. This case series highlights the association of vitamin B12 deficiency and its TTP-like presentations. Cases: The first case describes a 72-year-old man with shortness of breath and weakness. Diagnostics were notable for pancytopenia, schistocytes, and a low reticulocyte index. Intriguingly, total bilirubin was only mildly elevated however LDH and Haptoglobin were elevated and low, respectively. Additional diagnostic workup demonstrated an undetectable B12, elevated methylmalonic acid and elevated homocysteine. Initiation of B12 supplementation resolved his pancytopenia. The second case describes a 57-year-old man with chest tightness, dyspnea on exertion, and night sweats. Diagnostic evaluation demonstrated pancytopenia, schistocytes, a low reticulocyte index, and a remarkably low B12. He had associated high methylmalonic acid and homocysteine levels, confirming the diagnosis. B12 supplementation resolved his pancytopenia. Conclusion: The polysymptomatic presentation of vitamin B12 deficiency-induced pseudothrombotic microangiopathy highlights the vitamin’s role in essential physiological cellular functions. Rapid recognition of the underlying etiology of microangiopathic hemolytic anemia is necessary as treatment approaches diverge greatly.
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spelling doaj.art-3771bbb8a2e24453a00f500bf5c5e45f2023-01-02T02:50:32ZengGreater Baltimore Medical CenterJournal of Community Hospital Internal Medicine Perspectives2000-96662021-05-0111339740310.1080/20009666.2021.18931431893143Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpuraPegah Jahangiri0Rachel Hicks1Prabjot K. Batth2Christopher J. Haas3Medstar HealthSaba University School of MedicineSaba University School of MedicineMedStar HealthBackground: Thrombotic thrombocytopenic purpura (TTP) is a hematological emergency requiring prompt plasmapheresis. Conversely, vitamin B12 deficiency is a relatively benign diagnosis that can mimic microangiopathic hemolytic anemia, characterized by the presence of anemia, thrombocytopenia, indirect hyperbilirubinemia, markers of hemolysis, and schistocytes. This case series highlights the association of vitamin B12 deficiency and its TTP-like presentations. Cases: The first case describes a 72-year-old man with shortness of breath and weakness. Diagnostics were notable for pancytopenia, schistocytes, and a low reticulocyte index. Intriguingly, total bilirubin was only mildly elevated however LDH and Haptoglobin were elevated and low, respectively. Additional diagnostic workup demonstrated an undetectable B12, elevated methylmalonic acid and elevated homocysteine. Initiation of B12 supplementation resolved his pancytopenia. The second case describes a 57-year-old man with chest tightness, dyspnea on exertion, and night sweats. Diagnostic evaluation demonstrated pancytopenia, schistocytes, a low reticulocyte index, and a remarkably low B12. He had associated high methylmalonic acid and homocysteine levels, confirming the diagnosis. B12 supplementation resolved his pancytopenia. Conclusion: The polysymptomatic presentation of vitamin B12 deficiency-induced pseudothrombotic microangiopathy highlights the vitamin’s role in essential physiological cellular functions. Rapid recognition of the underlying etiology of microangiopathic hemolytic anemia is necessary as treatment approaches diverge greatly.http://dx.doi.org/10.1080/20009666.2021.1893143vitamin b12 deficiencythrombotic thrombocytopenic purpura (ttp)ttp-like syndromepancytopenia
spellingShingle Pegah Jahangiri
Rachel Hicks
Prabjot K. Batth
Christopher J. Haas
Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
Journal of Community Hospital Internal Medicine Perspectives
vitamin b12 deficiency
thrombotic thrombocytopenic purpura (ttp)
ttp-like syndrome
pancytopenia
title Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
title_full Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
title_fullStr Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
title_full_unstemmed Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
title_short Fooled by the fragments: vitamin B12 deficiency masquerading as thrombotic thrombocytopenic purpura
title_sort fooled by the fragments vitamin b12 deficiency masquerading as thrombotic thrombocytopenic purpura
topic vitamin b12 deficiency
thrombotic thrombocytopenic purpura (ttp)
ttp-like syndrome
pancytopenia
url http://dx.doi.org/10.1080/20009666.2021.1893143
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