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Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma

An 80-year-old man was admitted for acute subdural hematoma caused by a mild brain injury. His coagulation test showed an isolated prolongation of activated partial thromboplastin time (aPTT). Though the subdural hematoma did not progress, oozing bleed from the wound of tracheostomy continued. Failu...

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Detalles Bibliográficos
Autores principales: Sehara, Yoshihide, Hayashi, Yuka, Mimuro, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603318/
https://www.ncbi.nlm.nih.gov/pubmed/26491582
http://dx.doi.org/10.1155/2015/543927
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author Sehara, Yoshihide
Hayashi, Yuka
Mimuro, Jun
author_facet Sehara, Yoshihide
Hayashi, Yuka
Mimuro, Jun
author_sort Sehara, Yoshihide
collection PubMed
description An 80-year-old man was admitted for acute subdural hematoma caused by a mild brain injury. His coagulation test showed an isolated prolongation of activated partial thromboplastin time (aPTT). Though the subdural hematoma did not progress, oozing bleed from the wound of tracheostomy continued. Failure of correction on aPTT mixing test supported the presence of an inhibitor to a coagulation factor. Once the diagnosis of acquired hemophilia A (AHA) was made, steroid therapy was performed, which leads him to complete remission of AHA. Isolated prolongation of aPTT can be the key to diagnose a rare coagulopathy, such as AHA.
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spelling pubmed-46033182015-10-21 Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma Sehara, Yoshihide Hayashi, Yuka Mimuro, Jun Case Rep Neurol Med Case Report An 80-year-old man was admitted for acute subdural hematoma caused by a mild brain injury. His coagulation test showed an isolated prolongation of activated partial thromboplastin time (aPTT). Though the subdural hematoma did not progress, oozing bleed from the wound of tracheostomy continued. Failure of correction on aPTT mixing test supported the presence of an inhibitor to a coagulation factor. Once the diagnosis of acquired hemophilia A (AHA) was made, steroid therapy was performed, which leads him to complete remission of AHA. Isolated prolongation of aPTT can be the key to diagnose a rare coagulopathy, such as AHA. Hindawi Publishing Corporation 2015 2015-09-29 /pmc/articles/PMC4603318/ /pubmed/26491582 http://dx.doi.org/10.1155/2015/543927 Text en Copyright © 2015 Yoshihide Sehara et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Sehara, Yoshihide
Hayashi, Yuka
Mimuro, Jun
Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title_full Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title_fullStr Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title_full_unstemmed Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title_short Acquired Hemophilia A with a Rare Presentation of Acute Subdural Hematoma
title_sort acquired hemophilia a with a rare presentation of acute subdural hematoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603318/
https://www.ncbi.nlm.nih.gov/pubmed/26491582
http://dx.doi.org/10.1155/2015/543927
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