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Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review
Acquired hemophilia is a rare coagulation disorder that is not diagnosed by routine clinical laboratory tests. Thus, many perioperative or acute emergent bleeding complications remain unclear until the underlying cause is specified. We report two cases of postoperative bleeding in the context of den...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
UMF “Gr. T. Popa” Iasi Publishing House
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066585/ https://www.ncbi.nlm.nih.gov/pubmed/35529094 http://dx.doi.org/10.22551/2022.34.0901.10197 |
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author | Sucker, Christoph Bosch, Alexander Duecker, Christian Schüttler-Janikulla, Claus Schmitt, Ursula Litmathe, Jens |
author_facet | Sucker, Christoph Bosch, Alexander Duecker, Christian Schüttler-Janikulla, Claus Schmitt, Ursula Litmathe, Jens |
author_sort | Sucker, Christoph |
collection | PubMed |
description | Acquired hemophilia is a rare coagulation disorder that is not diagnosed by routine clinical laboratory tests. Thus, many perioperative or acute emergent bleeding complications remain unclear until the underlying cause is specified. We report two cases of postoperative bleeding in the context of dental surgery in which subsequent acquired hemophilia could be confirmed and present a short review from the literature. |
format | Online Article Text |
id | pubmed-9066585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | UMF “Gr. T. Popa” Iasi Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-90665852022-05-06 Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review Sucker, Christoph Bosch, Alexander Duecker, Christian Schüttler-Janikulla, Claus Schmitt, Ursula Litmathe, Jens Arch Clin Cases Case Report Acquired hemophilia is a rare coagulation disorder that is not diagnosed by routine clinical laboratory tests. Thus, many perioperative or acute emergent bleeding complications remain unclear until the underlying cause is specified. We report two cases of postoperative bleeding in the context of dental surgery in which subsequent acquired hemophilia could be confirmed and present a short review from the literature. UMF “Gr. T. Popa” Iasi Publishing House 2022-04-06 /pmc/articles/PMC9066585/ /pubmed/35529094 http://dx.doi.org/10.22551/2022.34.0901.10197 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Sucker, Christoph Bosch, Alexander Duecker, Christian Schüttler-Janikulla, Claus Schmitt, Ursula Litmathe, Jens Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title | Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title_full | Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title_fullStr | Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title_full_unstemmed | Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title_short | Acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
title_sort | acquired hemophilia as a rare cause of excessive bleeding during dentistry: report of two cases and short review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066585/ https://www.ncbi.nlm.nih.gov/pubmed/35529094 http://dx.doi.org/10.22551/2022.34.0901.10197 |
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