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Research Article Open access CC BY 4.0

Diagnosis and Management of an Acquired Factor XIII Deficiency in a Limited Resource Setting: A Case Report

C C Kariyawasan, P H D Athukorala, N L Priyantha, B L T Balasuriya

Asian Hematology Research Journal · pp. 224–228 · Published 2 Dec 2024

10.9734/ahrj/2024/v7i4185

Abstract

Factor XIII deficiency, a rare bleeding disorder, can be either immune – mediated or non -immune and present significant challenges due to potential life-threatening bleeding. This report underscores the importance of targeted management in FXIII deficiency, particularly in low- resource setting where advanced testing may be inaccessible. The case centers on 16-year-old boy with a history of mild bleeding who -presented with a subdural hemorrhage after a fall. Initial tests, including standard clotting profiles and screening for von Willebrand factor deficiency, were normal, prompting further investigation. A positive clot solubility test suggested Factor XIII deficiency. Due to limited facilities, FXIII assays were unavailable, so the patient was managed with fresh frozen plasma, cryoprecipitate, and tranexamic acid. Post-surgery bleeding revealed potential FXIII inhibitors, which were managed with additional plasma, cryoprecipitate, and oral prednisolone. The patient responded well and remained asymptomatic after discharge.

Factor XIII deficiency acquired factor XIII deficiency bleeding disorders

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