Affiliation:
1. Department of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
Abstract
AbstractMultiple myeloma (MM) is a clonal plasma cell disorder that commonly presents with anemia, renal failure, hypercalcemia, and lytic bone lesions. MM is also frequently associated with thrombotic complications; however, it may rarely present with bleeding diathesis. We report a case of a 42-year-old gentleman with relapsed immunoglobulin G lambda MM who presented with epistaxis, gingival bleeding, and oozing at the venepuncture site. Routine tests of coagulation revealed a prolonged prothrombin time (PT), activated partial thromboplastin time (aPTT), and thrombin time. The PT and aPTT failed to correct with pooled normal plasma and the patient was thus diagnosed to have an acquired heparin-like anticoagulant (HLAC). The source of this HLAC has long been debated, but recent data have demonstrated that this HLAC may be the paraproteins produced by the malignant plasma cells. The patient was treated with intravenous protamine sulfate, repeated cycles of plasma exchange, and a daratumumab-based quadruplet regimen but eventually succumbed to an intracranial hemorrhage. HLAC is a rare but potentially fatal complication of MM that must be considered when patients with MM present with bleeding diathesis.
Subject
Oncology,Pediatrics, Perinatology and Child Health
Reference19 articles.
1. Bleeding diathesis in multiple myeloma;M W Saif;J Hematother Stem Cell Res,2001
2. Isolation of a heparin-like anticoagulant from the plasma of a patient with metastatic bladder carcinoma;A Tefferi;Blood,1989
3. Acquired heparinlike anticoagulant in a patient with metastatic breast carcinoma;G M Rodgers;West J Med,1985
4. Heparin-like anticoagulant associated with AIDS;D de Prost;Thromb Haemost,1987
5. Hemostatic defects in dysproteinemias;H A Perkins;Blood,1970