Conclusions
The described PTs had the characteristics of distal PTs, appeared most probably after intraosseous hemorrhage. The presented case of multiple distal PTs is extremely rare. The most important factors favoring the apparition of multiple PTs were: high inhibitors level, shortage of bypassing agents, and severe osteoporosis. The spontaneous evolution of PTs was characterized by repeated episodes of hemorrhage and infection, and progressive growth. The conservative surgical approach (evacuation, drainage) was almost always inefficient. PTs could be solved only by complete excision/amputation. Alternative approaches to radical surgery, in patients with distal PTs and inhibitors merit to be discussed (antiangiogenic therapy, long-term therapy with bypassing agents, early conservative surgery — percutaneous management).
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Petrescu, C.A., Şerban, M., Ţepeneu, P., Schramm, W., BĂdeŢi, R., Popescu, B. (2005). Multiple Distal Pseudotumours in a Patient with Severe Hemophilia A and High Titer Inhibitors. In: Scharrer, I., Schramm, W. (eds) 34th Hemophilia Symposium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-27022-1_26
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