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Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency

The hematological manifestations of cobalamin (vitamin B12) deficiency may range from asymptomatic to life-threatening forms. Pseudothrombotic microangiopathy is a rare but severe presentation, characterized by the presence of hemolysis and schistocytosis, that is completely reversible after vitamin...

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Autores principales: Pereira Fontes, Carla, Fonseca, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439408/
https://www.ncbi.nlm.nih.gov/pubmed/34540418
http://dx.doi.org/10.7759/cureus.17184
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author Pereira Fontes, Carla
Fonseca, Samuel
author_facet Pereira Fontes, Carla
Fonseca, Samuel
author_sort Pereira Fontes, Carla
collection PubMed
description The hematological manifestations of cobalamin (vitamin B12) deficiency may range from asymptomatic to life-threatening forms. Pseudothrombotic microangiopathy is a rare but severe presentation, characterized by the presence of hemolysis and schistocytosis, that is completely reversible after vitamin supplementation. We present a challenging diagnostic approach of a 55-year-old man who presented with high hemolytic markers, pancytopenia, and schistocytes on the peripheral smear due to acquired cobalamin deficiency. Subsequent testing revealed positive anti-intrinsic factor and anti-parietal cell antibodies consistent with pernicious anemia. Cobalamin replacement led to the resolution of microangiopathic hemolysis and clinical improvement, thereby confirming the diagnosis. This case highlights the importance of early recognition of this syndrome, which is often misdiagnosed as true microangiopathic hemolytic anemia, confounding appropriate management.
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spelling pubmed-84394082021-09-16 Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency Pereira Fontes, Carla Fonseca, Samuel Cureus Internal Medicine The hematological manifestations of cobalamin (vitamin B12) deficiency may range from asymptomatic to life-threatening forms. Pseudothrombotic microangiopathy is a rare but severe presentation, characterized by the presence of hemolysis and schistocytosis, that is completely reversible after vitamin supplementation. We present a challenging diagnostic approach of a 55-year-old man who presented with high hemolytic markers, pancytopenia, and schistocytes on the peripheral smear due to acquired cobalamin deficiency. Subsequent testing revealed positive anti-intrinsic factor and anti-parietal cell antibodies consistent with pernicious anemia. Cobalamin replacement led to the resolution of microangiopathic hemolysis and clinical improvement, thereby confirming the diagnosis. This case highlights the importance of early recognition of this syndrome, which is often misdiagnosed as true microangiopathic hemolytic anemia, confounding appropriate management. Cureus 2021-08-14 /pmc/articles/PMC8439408/ /pubmed/34540418 http://dx.doi.org/10.7759/cureus.17184 Text en Copyright © 2021, Pereira Fontes et al. https://creativecommons.org/licenses/by/3.0/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 author and source are credited.
spellingShingle Internal Medicine
Pereira Fontes, Carla
Fonseca, Samuel
Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title_full Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title_fullStr Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title_full_unstemmed Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title_short Pseudothrombotic Microangiopathy as a Rare Presentation of Cobalamin Deficiency
title_sort pseudothrombotic microangiopathy as a rare presentation of cobalamin deficiency
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439408/
https://www.ncbi.nlm.nih.gov/pubmed/34540418
http://dx.doi.org/10.7759/cureus.17184
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