Imaging Advances in Light Chain Amyloidosis
Miaoling Qiu1,2, Kaini Shen3, Hua Yang1,2
1Department of Hematology, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.
Light chain amyloidosis diagnosis and prognosis rely on cardiac assessment. Advanced imaging techniques like echocardiography, MRI, and nuclear medicine offer quantitative tissue characterization for personalized treatment strategies.
Area of Science:
- Cardiology
- Oncology
- Radiology
Background:
- Light chain (AL) amyloidosis is a systemic plasma cell disorder.
- Cardiac involvement significantly impacts prognosis and survival outcomes.
- Heterogeneity in disease necessitates early diagnosis, risk stratification, and tailored therapy.
Purpose of the Study:
- To review recent advances in multimodality imaging for AL amyloidosis.
- To highlight the shift towards quantitative tissue characterization in imaging.
- To emphasize the role of imaging in guiding personalized patient management.
Main Methods:
- Review of current literature on echocardiography, MRI, and nuclear medicine imaging in AL amyloidosis.
- Synthesis of data on quantitative and multiparametric imaging techniques.
- Focus on non-invasive assessment of cardiac involvement.
Main Results:
- Multimodality imaging is crucial for non-invasive evaluation of AL amyloidosis.
- Imaging modalities provide insights beyond anatomical assessment.
- Quantitative tissue characterization is advancing patient management.
Conclusions:
- Advanced imaging is indispensable for diagnosing and managing AL amyloidosis.
- Personalized treatment strategies are increasingly guided by imaging data.
- Multimodality imaging enhances risk stratification and response assessment.
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