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Megakaryocyte Differentiation and Platelet Formation from Human Cord Blood-derived CD34+ Cells
Published on: December 27, 2017
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Acquired platelet dysfunction in newly diagnosed myeloma.
Joshua Mortimer1, Nicola Gray1, Michael Desborough2
1Department of Haematology Oxford University Hospitals NHS Foundation Trust Oxford UK.
Ejhaem
|July 18, 2022
Summary
Untreated plasma cell dyscrasias can cause acquired platelet disorders, leading to serious bleeding complications after procedures like bone marrow biopsy. Treatment reduced the paraprotein load, correcting platelet aggregation and improving outcomes.
Area of Science:
- Hematology
- Oncology
- Internal Medicine
Background:
- Plasma cell dyscrasias, such as multiple myeloma, are associated with various hematological complications.
- Bleeding disorders can arise secondary to underlying plasma cell dyscrasias, impacting patient safety during invasive procedures.
Purpose of the Study:
- To report a case of severe bleeding complication following bone marrow biopsy in a patient with newly diagnosed multiple myeloma.
- To investigate the association between paraproteinemia and acquired platelet dysfunction.
- To highlight the clinical significance of recognizing this risk in patients with untreated plasma cell dyscrasias.
Main Methods:
- A patient underwent bone marrow biopsy for suspected IgA paraprotein.
- Platelet function was assessed using light aggregometry.
- Treatment for multiple myeloma included antimyeloma therapy and plasma exchange.
Main Results:
- The patient experienced unexpected and severe bleeding post-biopsy.
- Abnormal platelet aggregometry suggested an acquired platelet disorder.
- Impaired platelet aggregation resolved with reduction of the paraprotein load.
Conclusions:
- Acquired platelet dysfunction is a potential complication of untreated plasma cell dyscrasias.
- Reduction of paraprotein load can restore normal platelet function.
- Clinicians should consider this risk in patients with plasma cell dyscrasias undergoing procedures.
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