# Mycobacterium florentinum pulmonary disease: a case report and review of the literature

**Authors:** Fabian Leo, Silke Polsfuss, Anne-Sophie Przewosnik, Christian Grohé, Christoph Lange

PMC · DOI: 10.1186/s12879-025-12321-3 · BMC Infectious Diseases · 2025-12-17

## TL;DR

A rare case of Mycobacterium florentinum lung disease was successfully treated with a combination therapy including inhaled amikacin, but co-infection with Aspergillus emerged during treatment.

## Contribution

Reports successful use of ALIS in treating M. florentinum and highlights the risk of Aspergillus co-infection.

## Key findings

- Combination therapy with ALIS led to rapid culture conversion in M. florentinum pulmonary disease.
- Aspergillus co-infection was diagnosed during treatment, requiring antifungal therapy for improvement.
- Treatment with ALIS may be considered for non-MAC NTM pulmonary diseases.

## Abstract

Following the initial description of Mycobacterium florentinum in 2005, very few clinical cases have been reported and the optimal antimicrobial treatment and clinical outcomes are uncertain. Amikacin liposome inhalation suspension (ALIS) has received approval for the treatment of Mycobacterium avium/intracellulare complex (MAC) pulmonary disease. However, there is little experience with its use for infections caused by less common nontuberculous mycobacteria (NTM). Moreover, the awareness of uncommon adverse effects is still limited.

A 69-year-old female patient suffering from nodular bronchiectatic Mycobacterium florentinum pulmonary disease was treated with azithromycin, ethambutol, and rifampicin, administered three times per week. After 13 months, owing to treatment failure, the therapy was changed to ALIS, moxifloxacin, and clofazimine. This resulted in rapid and sustained culture conversion. Concurrently, the patient exhibited increased cough and sputum, which was consistent with a clinical diagnosis of aspergillosis, as confirmed by evidence of Aspergillus fumigatus in respiratory specimens and a significant increase in serum Aspergillus IgG antibody levels. Following a six-month course of antifungal therapy, a marked improvement in the patient’s symptoms was observed.

As with MAC pulmonary disease, combination antimicrobial therapy including ALIS was successful in a patient affected by a difficult-to-treat pulmonary infection caused by Mycobacterium florentinum, a rare NTM pathogen. Combination antibiotic treatment including ALIS may also be considered for other difficult-to-treat, non-MAC NTM- pulmonary diseases. During treatment, patients should be monitored for the emergence of Aspergillus co-infection.

The online version contains supplementary material available at 10.1186/s12879-025-12321-3.

## Linked entities

- **Chemicals:** azithromycin (PubChem CID 447043), ethambutol (PubChem CID 14052), rifampicin (PubChem CID 135398735), moxifloxacin (PubChem CID 152946), clofazimine (PubChem CID 2794)
- **Diseases:** pulmonary disease (MONDO:0005275), aspergillosis (MONDO:0005657)
- **Species:** Mycobacterium florentinum (taxon 292462), Aspergillus fumigatus (taxon 746128)

## Full-text entities

- **Diseases:** pulmonary infection (MESH:D012141), MAC pulmonary disease (MESH:D015270), -infection (MESH:D007239), aspergillosis (MESH:D001228), Mycobacterium florentinum pulmonary disease (MESH:D008171), cough (MESH:D003371)
- **Chemicals:** Amikacin (MESH:D000583), ethambutol (MESH:D004977), rifampicin (MESH:D012293), moxifloxacin (MESH:D000077266), clofazimine (MESH:D002991), azithromycin (MESH:D017963)
- **Species:** Mycobacterium florentinum (species) [taxon 292462], Aspergillus fumigatus (species) [taxon 746128], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12822083/full.md

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Source: https://tomesphere.com/paper/PMC12822083