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Myelofibrosis and acquired hemophilia A: a case report
BACKGROUND: Myelofibrosis and acquired hemophilia A is a rare association. To the best of our knowledge only one case of myelofibrosis and acquired hemophilia A has been previously described. CASE PRESENTATION: A 66-year-old Caucasian man diagnosed with myelofibrosis evolving in acute myeloid leukem...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859983/ https://www.ncbi.nlm.nih.gov/pubmed/27154067 http://dx.doi.org/10.1186/s13256-016-0897-4 |
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author | Wrobel, Marie Comio, Emilie Gay, Valerie Baroudi, Noureddine Meyer, Pascal Chuniaud-Louche, Christine Hacini, Maya Pica, Gian Matteo |
author_facet | Wrobel, Marie Comio, Emilie Gay, Valerie Baroudi, Noureddine Meyer, Pascal Chuniaud-Louche, Christine Hacini, Maya Pica, Gian Matteo |
author_sort | Wrobel, Marie |
collection | PubMed |
description | BACKGROUND: Myelofibrosis and acquired hemophilia A is a rare association. To the best of our knowledge only one case of myelofibrosis and acquired hemophilia A has been previously described. CASE PRESENTATION: A 66-year-old Caucasian man diagnosed with myelofibrosis evolving in acute myeloid leukemia was referred to us for postoperative bleeding. Hemostatic studies showed prolonged activated partial thromboplastin time, decreased factor VIII coagulation, and a high factor VIII inhibitor titer; these findings led to a diagnosis of acquired hemophilia A for which he was treated with methylprednisolone and recombinant activated factor VII on admission. Due to a lack of response he was subsequently treated with rituximab combined with activated prothrombin complex concentrates. Furthermore, he received azacytidine to treat the underlying hematological malignancies. Immunosuppressive rituximab therapy resolved acquired hemophilia A with marked efficacy. CONCLUSIONS: Rapid and accurate diagnosis, effective hemostatic therapy, and timely treatment for underlying disease are important in the management of acquired hemophilia A secondary to hematological malignancy. |
format | Online Article Text |
id | pubmed-4859983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48599832016-05-08 Myelofibrosis and acquired hemophilia A: a case report Wrobel, Marie Comio, Emilie Gay, Valerie Baroudi, Noureddine Meyer, Pascal Chuniaud-Louche, Christine Hacini, Maya Pica, Gian Matteo J Med Case Rep Case Report BACKGROUND: Myelofibrosis and acquired hemophilia A is a rare association. To the best of our knowledge only one case of myelofibrosis and acquired hemophilia A has been previously described. CASE PRESENTATION: A 66-year-old Caucasian man diagnosed with myelofibrosis evolving in acute myeloid leukemia was referred to us for postoperative bleeding. Hemostatic studies showed prolonged activated partial thromboplastin time, decreased factor VIII coagulation, and a high factor VIII inhibitor titer; these findings led to a diagnosis of acquired hemophilia A for which he was treated with methylprednisolone and recombinant activated factor VII on admission. Due to a lack of response he was subsequently treated with rituximab combined with activated prothrombin complex concentrates. Furthermore, he received azacytidine to treat the underlying hematological malignancies. Immunosuppressive rituximab therapy resolved acquired hemophilia A with marked efficacy. CONCLUSIONS: Rapid and accurate diagnosis, effective hemostatic therapy, and timely treatment for underlying disease are important in the management of acquired hemophilia A secondary to hematological malignancy. BioMed Central 2016-05-07 /pmc/articles/PMC4859983/ /pubmed/27154067 http://dx.doi.org/10.1186/s13256-016-0897-4 Text en © Wrobel et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Wrobel, Marie Comio, Emilie Gay, Valerie Baroudi, Noureddine Meyer, Pascal Chuniaud-Louche, Christine Hacini, Maya Pica, Gian Matteo Myelofibrosis and acquired hemophilia A: a case report |
title | Myelofibrosis and acquired hemophilia A: a case report |
title_full | Myelofibrosis and acquired hemophilia A: a case report |
title_fullStr | Myelofibrosis and acquired hemophilia A: a case report |
title_full_unstemmed | Myelofibrosis and acquired hemophilia A: a case report |
title_short | Myelofibrosis and acquired hemophilia A: a case report |
title_sort | myelofibrosis and acquired hemophilia a: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859983/ https://www.ncbi.nlm.nih.gov/pubmed/27154067 http://dx.doi.org/10.1186/s13256-016-0897-4 |
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