# Refractory pleural effusion in malignant hypertension leading to an unexpected diagnosis of tuberculosis: A case report

**Authors:** Hiroki Ito, Kentaro Yano, Yuya Suzuki, Yoshitaka Taniguchi, Fumiya Sato, Shigemitsu Sato, Takuo Hirose, Ikuko Oba-Yabana, Takefumi Mori

PMC · DOI: 10.3892/etm.2025.12978 · Experimental and Therapeutic Medicine · 2025-09-19

## TL;DR

A patient with malignant hypertension and kidney damage was found to have tuberculosis, which was missed initially and led to treatment-resistant symptoms.

## Contribution

Highlights the importance of considering tuberculosis in patients with refractory hypertension and kidney dysfunction.

## Key findings

- Persistent pleural effusion and worsening kidney function led to the discovery of tuberculosis.
- Antituberculous therapy improved symptoms and renal function.
- Excessive diuretic use worsened kidney injury in this case.

## Abstract

Accelerated malignant hypertension frequently manifests as multiple organ dysfunctions. However, persistent symptoms despite appropriate antihypertensive therapy warrant investigation of concurrent pathologies, particularly in patients with risk factors for opportunistic infections. A 57-year-old woman with untreated hypertension presented in August 2024, with markedly elevated blood pressure (208/122 mmHg), systolic dysfunction (ejection fraction, 42.5%) and acute kidney injury (creatinine 4.74 mg/dl). Accelerated malignant hypertension with multiple organ damage was diagnosed based on these findings. Despite optimal antihypertensive and diuretic therapy, pleural effusion and renal function progressively worsened. Thoracentesis revealed a lymphocyte-predominant exudative effusion with elevated adenosine deaminase levels. Subsequent investigations confirmed tuberculous pleuritis and peritonitis, ultimately diagnosed as miliary tuberculosis. Excessive diuretic therapy for presumed heart failure-related effusion exacerbates renal injury. Following initiation of antituberculous therapy, pleural effusion and renal function markedly improved. This case emphasizes the importance of reevaluating initial diagnoses when the clinical responses are suboptimal. In patients with multiple risk factors, particularly diabetes mellitus and kidney dysfunction, concurrent tuberculosis should be considered for treatment-refractory symptoms.

## Linked entities

- **Diseases:** acute kidney injury (MONDO:0002492), tuberculosis (MONDO:0018076), pleuritis (MONDO:0000986), peritonitis (MONDO:1010128), miliary tuberculosis (MONDO:0005848), diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Genes:** ADA (adenosine deaminase) [NCBI Gene 100] {aka ADA1}
- **Diseases:** heart failure (MESH:D006333), effusion (MESH:D000080324), tuberculosis (MESH:D014376), Accelerated malignant hypertension (MESH:D006974), opportunistic infections (MESH:D009894), pleural effusion (MESH:D010996), peritonitis (MESH:D010538), multiple (MESH:D009104), systolic dysfunction (MESH:D006331), diabetes mellitus (MESH:D003920), hypertension (MESH:D006973), miliary tuberculosis (MESH:D014391), tuberculous pleuritis (MESH:D010998), kidney dysfunction (MESH:D007674), damage (MESH:D020263), organ (MESH:D000092124), acute kidney injury (MESH:D058186)
- **Chemicals:** creatinine (MESH:D003404), antituberculous (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12516476/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12516476/full.md

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Source: https://tomesphere.com/paper/PMC12516476