# Case Report: Contrast adenosine stress echocardiography revealing microvascular dysfunction in cardiac AL amyloidosis

**Authors:** Yuqian Dai, Yan Deng, Ni Lin, Feifei Che, Chunmei Li, Lixue Yin

PMC · DOI: 10.3389/fcvm.2026.1710211 · Frontiers in Cardiovascular Medicine · 2026-02-05

## TL;DR

A case report shows how a stress echocardiography test helped detect heart microvascular issues in a patient with a rare heart condition called AL amyloidosis.

## Contribution

Demonstrates the use of contrast adenosine stress echocardiography to detect microvascular dysfunction in cardiac AL amyloidosis.

## Key findings

- Contrast adenosine stress echocardiography revealed impaired myocardial perfusion in a patient with AL amyloidosis.
- Doppler-derived coronary flow velocity reserve was reduced, supporting the diagnosis of microvascular dysfunction.
- Findings aligned with cardiac MRI and lab results, confirming the utility of the echocardiography method.

## Abstract

Cardiac amyloidosis (CA) is a rare but increasingly recognized cause of restrictive cardiomyopathy. Noninvasive assessment of coronary microvascular dysfunction in CA can facilitate earlier diagnosis and improve disease monitoring. We present a case of light-chain (AL) cardiac amyloidosis manifesting as exertional angina with non-obstructive epicardial coronary arteries, in which contrast adenosine stress echocardiography combined with Doppler-derived coronary flow velocity reserve (CFVR) measurement revealed impaired myocardial perfusion and reduced CFVR. The findings were consistent with cardiac magnetic resonance (CMR) and laboratory results, confirming the diagnosis of CA. This case demonstrates the clinical application of contrast adenosine stress echocardiography as a practical adjunct to advanced imaging modalities for evaluating microvascular dysfunction in CA.

## Linked entities

- **Diseases:** AL amyloidosis (MONDO:0019438)

## Full-text entities

- **Genes:** NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}
- **Diseases:** pulmonary tuberculosis (MESH:D014397), myocardial ischemia (MESH:D017202), cardiac and renal involvement (MESH:C565423), inspiratory collapse (MESH:D001261), microvascular (MESH:D017566), hypertension (MESH:D006973), LV hypertrophy (MESH:D017379), diabetic cardiomyopathy (MESH:D058065), hepatomegaly (MESH:D006529), MI (MESH:D041781), restrictive cardiomyopathy (MESH:D002313), microvascular amyloid deposition (MESH:D058225), perfusion (MESH:D001480), ATTR (MESH:C567782), pulmonary hypertension (MESH:D006976), Amyloidosis (MESH:D000686), AL (MESH:D000075363), depression (MESH:D003866), tricuspid regurgitation (MESH:D014262), heart failure (MESH:D006333), conduction disturbances (MESH:C563984), hypertrophic cardiomyopathy (MESH:D002312), peripheral neuropathy (MESH:D010523), Cardiac involvement (MESH:D006331), coronary artery disease (MESH:D003324), amyloid (MESH:C000718787), dyspnea (MESH:D004417), multiple myeloma (MESH:D009101), ischemic (MESH:D002545), angina (MESH:D000787), edema (MESH:D004487), ischemic LV dilatation (MESH:C565277), pain (MESH:D010146), nephrotic (MESH:D009404), CMD (MESH:D003327), ischemia (MESH:D007511), stenosis (MESH:D003251), exertional angina (MESH:C564288), proteinuria (MESH:D011507), mitral regurgitation (MESH:D008944), pericardial effusion (MESH:D010490), autonomic and/or endothelial dysfunction (MESH:D001342), pleural effusion (MESH:D010996), diastolic dysfunction (MESH:D018487), myocardial infiltration (MESH:D017254), organ dysfunction (MESH:D009102), arrhythmias (MESH:D001145), lytic lesions (MESH:D009059), fatigue (MESH:D005221), chest pain (MESH:D002637), cardiomyopathy (MESH:D009202), hyperemia (MESH:D006940)
- **Chemicals:** dexamethasone (MESH:D003907), ethambutol (MESH:D004977), rifampicin (MESH:D012293), CA (-), Metoprolol (MESH:D008790), Amlodipine (MESH:D017311), valsartan (MESH:D000068756), gadolinium (MESH:D005682), Sacubitril (MESH:C000717211), daratumumab (MESH:C556306), SonoVue (MESH:C420843), Adenosine (MESH:D000241), isoniazid (MESH:D007538), cyclophosphamide (MESH:D003520), bortezomib (MESH:D000069286)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916374/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916374/full.md

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Source: https://tomesphere.com/paper/PMC12916374