Table 1.
Baseline patient characteristics and interventions
| Patient No. 1 71 years, male |
Patient No. 2 59 years, male |
Normal range | |
|---|---|---|---|
|
Paraprotein Type of monoclonal gammopathy |
IgG-kappa SMM |
IgG-kappa Solitary plasmacytoma with minimal marrow involvement |
– |
| Bone marrow plasma cells (in %) | 50 | 5 | – |
| aPTT | 50.9 s | 42.6 s | 27.0–41.0 s |
| FVIII activity (in %) | 14 | 15 | 60–230 |
| vWF:Ag activity (in %) | 10 | 17 | 60–180 |
| vWF:Act (in %) | 4 | 21 | 48–170 |
| vWF:Rco (in %) | 10 | < 10 | 60–180 |
| vWF multimer studies | No large multimers present | Normal distribution pattern | – |
| Bleeding symptoms | Extensive bleeding history including life-threatening hemorrhagic shock during mechanical ventilation | Perisurgical hematoma following surgery for pathological femoral fracture | – |
| Intervention | Antimyeloma treatment | Antimyeloma treatment and ASCT | – |
| Outcome | Complete normalization of coagulation studies, no further bleeding complications | Complete normalization of coagulation studies, no further bleeding complications | – |
MGUS monoclonal gammopathy of undetermined significance, SMM smoldering multiple myeloma, aPTT activated partial thromboplastin time, FVIII factor VIII, vWF:Ag von Willebrand factor antigen, vWF:Act von Willebrand factor activity, vWF:RCo von Willebrand factor ristocetin cofactor activity