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Challenges in management of unusual acquired factor V deficiency: A case report

RATIONALE: Acquired inhibitors of coagulation are antibodies that either inhibit the activity or increase the clearance of a clotting factor. Acquired factor V deficiency is a rare coagulation disorder, and it can sometimes be life threatening. PATIENT CONCERNS: We describe a case of a 90-year-old J...

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Autores principales: Takemoto, Kiyoshi, Hamada, Osamu, Kitamura, Koichi, Fujiwara, Naoki, Miyakawa, Yoshitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831250/
https://www.ncbi.nlm.nih.gov/pubmed/31027075
http://dx.doi.org/10.1097/MD.0000000000015259
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author Takemoto, Kiyoshi
Hamada, Osamu
Kitamura, Koichi
Fujiwara, Naoki
Miyakawa, Yoshitaka
author_facet Takemoto, Kiyoshi
Hamada, Osamu
Kitamura, Koichi
Fujiwara, Naoki
Miyakawa, Yoshitaka
author_sort Takemoto, Kiyoshi
collection PubMed
description RATIONALE: Acquired inhibitors of coagulation are antibodies that either inhibit the activity or increase the clearance of a clotting factor. Acquired factor V deficiency is a rare coagulation disorder, and it can sometimes be life threatening. PATIENT CONCERNS: We describe a case of a 90-year-old Japanese male with acquired factor V deficiency. He was previously misdiagnosed with congenital factor V deficiency when he presented with hemoptysis and a negative factor V inhibitor test result at a different hospital 5 years earlier. Coagulopathy recurred with ecchymosis when he sustained a bruise after falling on a bush. DIAGNOSIS: Although the factor V inhibitor test result was negative and a mixing study suggested a deficiency pattern, we diagnosed the patient with acquired factor V deficiency on the basis of no history of bleeding diathesis, a lack of response to multiple fresh frozen plasma transfusion, and clinical response to corticosteroid therapy. INTERVENTIONS: Intravenous methylprednisolone was administered at 500 mg/day for 3 days, followed by oral prednisolone at 1 mg/kg/day. OUTCOMES: Coagulation test results improved and symptoms resolved 2 weeks after corticosteroid administration. LESSONS: This case report suggests that clearance-facilitating antibodies exist without the presence of neutralizing inhibitors. When patients present with coagulation factor V deficiency in the absence of coagulation inhibitors, acquired factor V deficiency should also be considered.
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spelling pubmed-68312502019-11-19 Challenges in management of unusual acquired factor V deficiency: A case report Takemoto, Kiyoshi Hamada, Osamu Kitamura, Koichi Fujiwara, Naoki Miyakawa, Yoshitaka Medicine (Baltimore) 4800 RATIONALE: Acquired inhibitors of coagulation are antibodies that either inhibit the activity or increase the clearance of a clotting factor. Acquired factor V deficiency is a rare coagulation disorder, and it can sometimes be life threatening. PATIENT CONCERNS: We describe a case of a 90-year-old Japanese male with acquired factor V deficiency. He was previously misdiagnosed with congenital factor V deficiency when he presented with hemoptysis and a negative factor V inhibitor test result at a different hospital 5 years earlier. Coagulopathy recurred with ecchymosis when he sustained a bruise after falling on a bush. DIAGNOSIS: Although the factor V inhibitor test result was negative and a mixing study suggested a deficiency pattern, we diagnosed the patient with acquired factor V deficiency on the basis of no history of bleeding diathesis, a lack of response to multiple fresh frozen plasma transfusion, and clinical response to corticosteroid therapy. INTERVENTIONS: Intravenous methylprednisolone was administered at 500 mg/day for 3 days, followed by oral prednisolone at 1 mg/kg/day. OUTCOMES: Coagulation test results improved and symptoms resolved 2 weeks after corticosteroid administration. LESSONS: This case report suggests that clearance-facilitating antibodies exist without the presence of neutralizing inhibitors. When patients present with coagulation factor V deficiency in the absence of coagulation inhibitors, acquired factor V deficiency should also be considered. Wolters Kluwer Health 2019-04-26 /pmc/articles/PMC6831250/ /pubmed/31027075 http://dx.doi.org/10.1097/MD.0000000000015259 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 4800
Takemoto, Kiyoshi
Hamada, Osamu
Kitamura, Koichi
Fujiwara, Naoki
Miyakawa, Yoshitaka
Challenges in management of unusual acquired factor V deficiency: A case report
title Challenges in management of unusual acquired factor V deficiency: A case report
title_full Challenges in management of unusual acquired factor V deficiency: A case report
title_fullStr Challenges in management of unusual acquired factor V deficiency: A case report
title_full_unstemmed Challenges in management of unusual acquired factor V deficiency: A case report
title_short Challenges in management of unusual acquired factor V deficiency: A case report
title_sort challenges in management of unusual acquired factor v deficiency: a case report
topic 4800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831250/
https://www.ncbi.nlm.nih.gov/pubmed/31027075
http://dx.doi.org/10.1097/MD.0000000000015259
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