Lupus anticoagulant hypoprothrombinemia syndrome: A case report

Lupus anticoagulant hypoprothrombinemia syndrome (LAHPS) is a rare entity associated with an increased risk of hemorrhage. Corticosteroids have been used in its treatment with favorable results. We present the case of a 54‐year‐old female patient with a personal history of Lupus diagnosed with LAHPS...

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Detalles Bibliográficos
Autores principales: Acedo, Natalia, Alonso, Alejandro, Feijoó, Eliana Samantha, García, Cristina, Ortiz, Ana M., Alegre, Adrián
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082346/
https://www.ncbi.nlm.nih.gov/pubmed/37038533
http://dx.doi.org/10.1002/ccr3.7071
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author Acedo, Natalia
Alonso, Alejandro
Feijoó, Eliana Samantha
García, Cristina
Ortiz, Ana M.
Alegre, Adrián
author_facet Acedo, Natalia
Alonso, Alejandro
Feijoó, Eliana Samantha
García, Cristina
Ortiz, Ana M.
Alegre, Adrián
author_sort Acedo, Natalia
collection PubMed
description Lupus anticoagulant hypoprothrombinemia syndrome (LAHPS) is a rare entity associated with an increased risk of hemorrhage. Corticosteroids have been used in its treatment with favorable results. We present the case of a 54‐year‐old female patient with a personal history of Lupus diagnosed with LAHPS following an episode of cerebellar hemorrhage.
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spelling pubmed-100823462023-04-09 Lupus anticoagulant hypoprothrombinemia syndrome: A case report Acedo, Natalia Alonso, Alejandro Feijoó, Eliana Samantha García, Cristina Ortiz, Ana M. Alegre, Adrián Clin Case Rep Case Report Lupus anticoagulant hypoprothrombinemia syndrome (LAHPS) is a rare entity associated with an increased risk of hemorrhage. Corticosteroids have been used in its treatment with favorable results. We present the case of a 54‐year‐old female patient with a personal history of Lupus diagnosed with LAHPS following an episode of cerebellar hemorrhage. John Wiley and Sons Inc. 2023-04-07 /pmc/articles/PMC10082346/ /pubmed/37038533 http://dx.doi.org/10.1002/ccr3.7071 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Acedo, Natalia
Alonso, Alejandro
Feijoó, Eliana Samantha
García, Cristina
Ortiz, Ana M.
Alegre, Adrián
Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title_full Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title_fullStr Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title_full_unstemmed Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title_short Lupus anticoagulant hypoprothrombinemia syndrome: A case report
title_sort lupus anticoagulant hypoprothrombinemia syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082346/
https://www.ncbi.nlm.nih.gov/pubmed/37038533
http://dx.doi.org/10.1002/ccr3.7071
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