# Chronic Brucella infection associated with amyloid light chain cardiac amyloidosis: a case report

**Authors:** RuiXia He, HaiJun Wang, LingMin Wu, Li Li, XinYuan Xu, GuoLi Ma, BaYaEr Qi, LiNa Ji, XiaoPing Liu

PMC · DOI: 10.3389/fcvm.2026.1703993 · 2026-03-12

## TL;DR

A 69-year-old man with chronic Brucella infection developed AL-type cardiac amyloidosis, raising questions about a possible link between the two conditions.

## Contribution

This case report highlights a potential, previously unexplored connection between chronic Brucella infection and AL-type cardiac amyloidosis.

## Key findings

- Chronic Brucella infection and AL-type cardiac amyloidosis occurred in the same patient with overlapping clinical onset.
- Myocardial biopsy confirmed AL amyloidosis, while genetic testing ruled out other inherited cardiomyopathies.
- The patient showed poor response to myocarditis-targeted treatment, suggesting a distinct underlying pathology.

## Abstract

Amyloidosis is a rare group of diseases characterized by extracellular deposition of amyloid fibrils. The most common types are amyloid light chain (AL) and transthyretin (ATTR), while serum amyloid A (AA) type is relatively rare. Infections are often associated with AA amyloidosis, whereas AL amyloidosis typically results from abnormal proliferation of monoclonal plasma cells. However, the relationship between AL amyloidosis and infections remains unclear.

We present the case of a 69-year-old male patient with chronic brucellosis complicated by heart failure. Laboratory tests showed significantly elevated myocardial enzymes and N-terminal pro-B type natriuretic peptide. Cardiac echocardiography and cardiac magnetic resonance imaging revealed abnormal myocardial hypertrophy, and the patient showed poor response to myocarditis-targeted treatment.

Genetic testing for inherited cardiomyopathies ruled out Fabry disease, hereditary hypertrophic cardiomyopathy, and ATTR amyloidosis-associated abnormal genes. Serum immunofixation electrophoresis indicated positivity for lambda light chain. AL cardiac amyloidosis was confirmed by myocardial biopsy.

We report a case of chronic Brucella infection and AL-type cardiac amyloidosis, with a high overlap in clinical onset time. However, additional studies are needed to confirm the potential relationship between Brucella infection and AL-type cardiac amyloidosis.

## Linked entities

- **Diseases:** amyloidosis (MONDO:0019065), AL amyloidosis (MONDO:0019438), AA amyloidosis (MONDO:0019439), Fabry disease (MONDO:0010526), hereditary hypertrophic cardiomyopathy (MONDO:0024573), myocarditis (MONDO:0004496)

## Full-text entities

- **Genes:** TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}
- **Diseases:** Amyloidosis (MESH:D000686), Brucella infection (MESH:D002006), AL amyloidosis (MESH:D000075363), ATTR amyloidosis (MESH:C567782), Infections (MESH:D007239), inherited cardiomyopathies (MESH:D009202), abnormal (MESH:D000014), Fabry disease (MESH:D000795), hereditary hypertrophic cardiomyopathy (MESH:D009386), AA (MESH:C000718787), heart failure (MESH:D006333), myocarditis (MESH:D009205), myocardial hypertrophy (MESH:D006984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13018100/full.md

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Source: https://tomesphere.com/paper/PMC13018100