# Rare secondary pituitary abscess arising in a craniopharyngioma: A case report and literature review

**Authors:** Rui Fan, Runsheng Zhao, Yan Zhong, Weiqing Wan

PMC · DOI: 10.3892/etm.2025.12908 · Experimental and Therapeutic Medicine · 2025-06-19

## TL;DR

A rare case of a pituitary abscess arising from a craniopharyngioma is reported, emphasizing the need for timely diagnosis and surgical treatment.

## Contribution

This is one of the few reported cases of a pituitary abscess secondary to a papillary craniopharyngioma.

## Key findings

- The patient showed clinical improvement after surgery and antibiotic therapy.
- Histopathology confirmed a papillary craniopharyngioma with inflammatory infiltration.
- Residual pituitary insufficiency and diabetes insipidus required long-term management.

## Abstract

A pituitary abscess is an extremely rare condition, classified as either primary or secondary. Secondary pituitary abscesses can arise from pre-existing pituitary lesions such as craniopharyngiomas. The present study describes the case of a 59-year-old man with a secondary pituitary abscess originating from a craniopharyngioma, presenting with a 10-month history of progressive visual decline, dizziness, headaches, nausea and vomiting. Although there were no overt endocrine symptoms, hormonal evaluation revealed hypothyroidism and growth hormone axis suppression, along with elevated prolactin levels due to pituitary stalk effect. MRI showed chronic inflammation in the sellar and suprasellar regions. The patient was initially treated with antibiotics, but symptoms persisted, necessitating craniotomy. Intraoperatively, a cystic structure was incised, releasing white purulent material. Histopathology confirmed a papillary craniopharyngioma with marked inflammatory infiltration. Postoperatively, the patient showed clinical improvement with antibiotic therapy; however, residual pituitary insufficiency and mild diabetes insipidus required long-term management. This case underscores the importance of considering secondary pituitary abscesses in the differential diagnosis of sellar lesions with atypical presentations. It is one of the few reported cases of a pituitary abscess secondary to a papillary craniopharyngioma, highlighting the critical role of timely surgical intervention and the diagnostic value of histopathological confirmation. The publication of this case provides new insights into the diagnostic challenges and management strategies for this rare but life-threatening condition.

## Linked entities

- **Diseases:** hypothyroidism (MONDO:0005420), diabetes insipidus (MONDO:0004782), craniopharyngioma (MONDO:0018907)

## Full-text entities

- **Genes:** PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}
- **Diseases:** craniopharyngioma (MESH:D003397), pituitary abscess (MESH:D000038), sellar lesions (MESH:D009059), pituitary lesions (MESH:D010900), dizziness (MESH:D004244), pituitary insufficiency (MESH:D007018), hypothyroidism (MESH:D007037), visual decline (MESH:D014786), growth hormone axis suppression (MESH:D004393), diabetes insipidus (MESH:D003919), vomiting (MESH:D014839), nausea (MESH:D009325), headaches (MESH:D006261), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12209761/full.md

## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12209761/full.md

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Source: https://tomesphere.com/paper/PMC12209761