Publication:
Successful treatment of factor x deficiency in a patient with lymphoplasmacytic lymphoma with bendamustine plus rituximab regimen: A case report and literature review

dc.contributor.authorTarinee Rungjirajittranonen_US
dc.contributor.authorYingyong Chinthammitren_US
dc.contributor.authorChattree Hantaweepanten_US
dc.contributor.otherSiriraj Hospitalen_US
dc.date.accessioned2022-08-04T11:04:37Z
dc.date.available2022-08-04T11:04:37Z
dc.date.issued2021-01-01en_US
dc.description.abstractBackground: Acquired factor X deficiency is an uncommon condition, and affected indi-viduals have severe and spontaneous bleeding. The associated conditions include malig-nancy, infection, burn, and inflammatory bowel disease. Many previous studies reported association between lymphoproliferative disease and factor X disappearance. Amyloid deposition causing factor X absorption was the most common mechanism. Here, we report a case of stage IV lymphoplasmacytic lymphoma (LPL) with factor X deficiency who was successfully treated with bendamustine plus rituximab (BR) regimen. Case Presentation: A 52-year-old Thai woman presented with heavy menorrhea, hoarseness, and widespread ecchymosis at her extremities. On physical examination, the patient had bilateral periorbital purpura and vocal cord hematoma. Coagulation testing showed prolonged prothrom-bin time (PT) and prolonged activated thromboplastin time (aPTT); however, after mixing with 1:1 normal pooled plasma, PT and aPTT were both corrected to normal levels. Factor assays demonstrated markedly decreased factor X levels, but no presence of factor X inhibitor. Bone marrow examination revealed numerous abnormal lymphoplasmacytoid lymphocytes with kappa light chain expression. Serum free light chain assay also showed kappa light chain restriction [kappa 716.16 mg/L, lambda 16.96 mg/L, ratio 42.23 (0.26–1.65)]. The patient was diagnosed as lymphoplasmacytic lymphoma with factor X deficiency. She received chemother-apy with 6 cycles of bendamustine plus rituximab (BR) regimen. The patient responded favorably to treatment, she remains in lymphoma remission at one year after diagnosis, and her factor X level was more than 20%. Conclusion: We performed a literature review to identify previous case reports about lymphoma-associated factor X deficiency or inhibitor to determine a possible explanation in our patient. It is important to emphasize that when patients present with acquired factor deficiency, including factor X, lymphoproliferative disease is commonly one of the under-lying conditions. Furthermore, the recovery of coagulation factor deficiency is possible if successful remission of lymphoma can be achieved.en_US
dc.identifier.citationJournal of Blood Medicine. Vol.12, (2021), 875-881en_US
dc.identifier.doi10.2147/JBM.S336635en_US
dc.identifier.issn11792736en_US
dc.identifier.other2-s2.0-85119686059en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/78562
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119686059&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleSuccessful treatment of factor x deficiency in a patient with lymphoplasmacytic lymphoma with bendamustine plus rituximab regimen: A case report and literature reviewen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119686059&origin=inwarden_US

Files

Collections