Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis

Acquired coagulopathies resulting from factor X deficiency are rare and typically associated with amyloidosis or plasma cell dyscrasia. Factor X plays a pivotal role in the coagulation cascade, converting prothrombin into thrombin and facilitating the formation of fibrinogen and thrombus. While its...

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Main Authors: P. Rossignon, F. Grandjean, A. Claessens, N. Weynants
Format: Article
Language:English
Published: Wiley 2023-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2023/5510654
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author P. Rossignon
F. Grandjean
A. Claessens
N. Weynants
author_facet P. Rossignon
F. Grandjean
A. Claessens
N. Weynants
author_sort P. Rossignon
collection DOAJ
description Acquired coagulopathies resulting from factor X deficiency are rare and typically associated with amyloidosis or plasma cell dyscrasia. Factor X plays a pivotal role in the coagulation cascade, converting prothrombin into thrombin and facilitating the formation of fibrinogen and thrombus. While its occurrence following common infections is extremely rare, isolated cases have been documented. We present a rare case of bleeding diathesis in a patient with community-acquired pneumonia, where prolonged activated partial thromboplastin time (aPTT) and prothrombin time (PT) led to the diagnosis of an infectious-triggered acquired circulating inhibitor targeting factor X. Prompt treatment with methylprednisolone effectively controlled the inhibitor without recurrence. This case report provides insights into the diagnostic strategies, differential algorithm, and therapeutic approaches for managing this rare coagulopathy.
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series Case Reports in Hematology
spelling doaj-art-5bf1571515d74da1bf6115fc4163ec522025-08-20T03:34:28ZengWileyCase Reports in Hematology2090-65792023-01-01202310.1155/2023/5510654Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic DiathesisP. Rossignon0F. Grandjean1A. Claessens2N. Weynants3Hematology-Oncology Department and Cardiology DepartmentDepartment of Clinical BiologyDepartment of Clinical BiologyDepartment of Clinical BiologyAcquired coagulopathies resulting from factor X deficiency are rare and typically associated with amyloidosis or plasma cell dyscrasia. Factor X plays a pivotal role in the coagulation cascade, converting prothrombin into thrombin and facilitating the formation of fibrinogen and thrombus. While its occurrence following common infections is extremely rare, isolated cases have been documented. We present a rare case of bleeding diathesis in a patient with community-acquired pneumonia, where prolonged activated partial thromboplastin time (aPTT) and prothrombin time (PT) led to the diagnosis of an infectious-triggered acquired circulating inhibitor targeting factor X. Prompt treatment with methylprednisolone effectively controlled the inhibitor without recurrence. This case report provides insights into the diagnostic strategies, differential algorithm, and therapeutic approaches for managing this rare coagulopathy.http://dx.doi.org/10.1155/2023/5510654
spellingShingle P. Rossignon
F. Grandjean
A. Claessens
N. Weynants
Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
Case Reports in Hematology
title Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
title_full Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
title_fullStr Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
title_full_unstemmed Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
title_short Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
title_sort circulating inhibitor against factor x a rare cause of hemorrhagic diathesis
url http://dx.doi.org/10.1155/2023/5510654
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