Cargando…
Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature
Hypofibrinogenemia and Factor XI deficiency are rare defects of hemostasis, potentially leading to spontaneous bleeding manifestations and increased bleeding risk during surgery, dentistry, and interventions. Due to the different mode of inheritance, the concomitance of both defects is extremely rar...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
UMF “Gr. T. Popa” Iasi Publishing House
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315684/ https://www.ncbi.nlm.nih.gov/pubmed/37405328 http://dx.doi.org/10.22551/2023.39.1002.10253 |
_version_ | 1785067549995565056 |
---|---|
author | Sucker, Christoph Geisen, Christof Litmathe, Jens Schmitt, Ursula |
author_facet | Sucker, Christoph Geisen, Christof Litmathe, Jens Schmitt, Ursula |
author_sort | Sucker, Christoph |
collection | PubMed |
description | Hypofibrinogenemia and Factor XI deficiency are rare defects of hemostasis, potentially leading to spontaneous bleeding manifestations and increased bleeding risk during surgery, dentistry, and interventions. Due to the different mode of inheritance, the concomitance of both defects is extremely rare and the clinical management of combined hypofibrinogenemia and factor XI deficiency is not standardized. Here, we report a rare case of concomitant genetically determined hypofibrinogenemia and factor XI deficiency as a cause of increased spontaneous bleeding and bleeding complications during dentistry. The diagnostic procedure including screening assays, single clotting factor determinations, genetic analyses, and also use of thrombin generation assays (TGA) are described. Also, we present our considerations regarding the development of an adequate prophylaxis of bleeding with fibrinogen concentrate in this case. The literature regarding the issue is briefly discussed. |
format | Online Article Text |
id | pubmed-10315684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | UMF “Gr. T. Popa” Iasi Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-103156842023-07-04 Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature Sucker, Christoph Geisen, Christof Litmathe, Jens Schmitt, Ursula Arch Clin Cases Case Report Hypofibrinogenemia and Factor XI deficiency are rare defects of hemostasis, potentially leading to spontaneous bleeding manifestations and increased bleeding risk during surgery, dentistry, and interventions. Due to the different mode of inheritance, the concomitance of both defects is extremely rare and the clinical management of combined hypofibrinogenemia and factor XI deficiency is not standardized. Here, we report a rare case of concomitant genetically determined hypofibrinogenemia and factor XI deficiency as a cause of increased spontaneous bleeding and bleeding complications during dentistry. The diagnostic procedure including screening assays, single clotting factor determinations, genetic analyses, and also use of thrombin generation assays (TGA) are described. Also, we present our considerations regarding the development of an adequate prophylaxis of bleeding with fibrinogen concentrate in this case. The literature regarding the issue is briefly discussed. UMF “Gr. T. Popa” Iasi Publishing House 2023-07-03 /pmc/articles/PMC10315684/ /pubmed/37405328 http://dx.doi.org/10.22551/2023.39.1002.10253 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 Geisen, Christof Litmathe, Jens Schmitt, Ursula Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title | Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title_full | Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title_fullStr | Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title_full_unstemmed | Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title_short | Concomitant hypofibrinogenemia and factor XI deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
title_sort | concomitant hypofibrinogenemia and factor xi deficiency as rare cause of bleeding during urgent dentistry: case report and short review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315684/ https://www.ncbi.nlm.nih.gov/pubmed/37405328 http://dx.doi.org/10.22551/2023.39.1002.10253 |
work_keys_str_mv | AT suckerchristoph concomitanthypofibrinogenemiaandfactorxideficiencyasrarecauseofbleedingduringurgentdentistrycasereportandshortreviewoftheliterature AT geisenchristof concomitanthypofibrinogenemiaandfactorxideficiencyasrarecauseofbleedingduringurgentdentistrycasereportandshortreviewoftheliterature AT litmathejens concomitanthypofibrinogenemiaandfactorxideficiencyasrarecauseofbleedingduringurgentdentistrycasereportandshortreviewoftheliterature AT schmittursula concomitanthypofibrinogenemiaandfactorxideficiencyasrarecauseofbleedingduringurgentdentistrycasereportandshortreviewoftheliterature |