# Pulmonary Fibrosis in a Patient With a Prolactinoma on Dopamine Agonists: Coincidence or Consequence

**Authors:** Ravi Shah, Amanjit Bal, Durairaj Arjunan, Jayaditya Ghosh, Ashley B Grossman, Pinaki Dutta

PMC · DOI: 10.1210/jcemcr/luaf067 · JCEM Case Reports · 2025-04-15

## TL;DR

A patient with a prolactinoma developed lung fibrosis after long-term dopamine agonist therapy, suggesting a possible drug-induced cause.

## Contribution

This case highlights the rare but serious risk of interstitial lung disease from dopamine agonists in prolactinoma patients.

## Key findings

- The patient developed usual interstitial pneumonia after decades of dopamine agonist use.
- Autoimmune and environmental causes were largely excluded, pointing to a drug-induced etiology.
- Discontinuation of cabergoline was followed by continued monitoring of the patient's condition.

## Abstract

Prolactinomas are the most common functional pituitary tumor and are typically managed with dopamine agonists such as bromocriptine or cabergoline. Although these agents are generally well tolerated and effective in reducing prolactin levels and often tumor size, they have been implicated in rare but serious fibrotic complications, including interstitial lung disease (ILD). We describe a 65-year-old man with a longstanding prolactinoma who received cumulative high-dose bromocriptine and cabergoline therapy over several decades. Despite initial tumor shrinkage and partial biochemical control of hyperprolactinemia with dopamine agonists, stereotactic radiosurgery, and transsphenoidal surgery, the patient developed progressive exertional dyspnea and cough, accompanied by imaging and histopathological findings consistent with “usual interstitial pneumonia” (UIP). Autoimmune and environmental causes were largely excluded, suggesting a drug-induced etiology.

Following discontinuation of cabergoline, the patient has been on continued surveillance of his prolactin levels and tumor status, with symptomatic treatment of his UIP.

This case underscores the potential for dopamine agonist–associated ILD, even in patients with prolactinomas who generally receive lower weekly doses than those used in Parkinson’s and related diseases. Early recognition of respiratory symptoms, pulmonary function, and radiological investigations are indicated in selected symptomatic cases.

## Linked entities

- **Chemicals:** bromocriptine (PubChem CID 31101), cabergoline (PubChem CID 54746)
- **Diseases:** pulmonary fibrosis (MONDO:0002771), prolactinoma (MONDO:0010911), interstitial lung disease (MONDO:0015925)

## Full-text entities

- **Genes:** PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}
- **Diseases:** Prolactinoma (MESH:D015175), cough (MESH:D003371), hyperprolactinemia (MESH:D006966), fibrotic complications (MESH:D008107), tumor (MESH:D009369), Parkinson's and related diseases (MESH:D010300), ILD (MESH:D017563), dyspnea (MESH:D004417), pituitary tumor (MESH:D010911), UIP (MESH:D054990), Pulmonary Fibrosis (MESH:D011658)
- **Chemicals:** cabergoline (MESH:D000077465), bromocriptine (MESH:D001971)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11997647/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11997647/full.md

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Source: https://tomesphere.com/paper/PMC11997647