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[Hemostasis disorders in patients with systemic AL-amyloidosis]
I G Rekhtina1, V A Khyshova1, N I Zozulya1
1National Medical Research Center for Hematology.
Terapevticheskii Arkhiv
|December 30, 2023
Summary
Cutaneous hemorrhagic syndrome is common in AL-amyloidosis patients, often linked to hypercoagulation and increased thrombotic risk. This finding highlights the importance of monitoring hemostasis in these patients.
Area of Science:
- Hematology
- Internal Medicine
- Oncology
Context:
- Systemic AL-amyloidosis is a plasma cell disorder characterized by amyloid deposition.
- Hemostatic abnormalities are frequently observed in AL-amyloidosis patients.
- Understanding these complications is crucial for patient management.
Purpose:
- To investigate the frequency and characteristics of hemorrhagic and thrombotic complications in AL-amyloidosis.
- To correlate these complications with laboratory hemostasis parameters.
- To identify potential pathogenetic links between bleeding, thrombosis, and organ damage.
Summary:
- 50% of AL-amyloidosis patients experienced cutaneous hemorrhagic syndrome (vascular purpura).
- 17.5% had thrombotic events, including leg vein thrombosis and ischemic stroke.
- Hypercoagulation was prevalent (56%), associated with bleeding and thrombosis risk.
Impact:
- Establishes cutaneous hemorrhagic syndrome as a key hemostasis disorder in AL-amyloidosis.
- Reveals a link between skin hemorrhages, nephrotic syndrome, and hypercoagulable states.
- Suggests hypercoagulation and bleeding risk are intertwined, impacting patient outcomes.
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