# Case Report: A case series of Lhermitte–Duclos disease with surgical intervention

**Authors:** Ziyang Chen, Min Guo, Xingke Li, Cheng Lin, Guili Feng, Jianzhi Zhou, Hainan Li, Baijie Chen, Lirong Liu, Linbo Cai, Lei Wang, Hui Ouyang, Yanfeng Fan

PMC · DOI: 10.3389/fonc.2025.1552495 · Frontiers in Oncology · 2025-10-23

## TL;DR

This case series describes three adults with Lhermitte–Duclos disease, focusing on imaging, surgery, and PTEN testing outcomes.

## Contribution

The study provides insights into surgical decision-making and PTEN evaluation in adult LDD patients.

## Key findings

- All three patients showed the characteristic 'tiger-striped' MRI appearance of LDD.
- PTEN testing supported a link to PTEN hamartoma tumor syndrome in one case.
- Surgical outcomes varied, with two patients improving and one having poor neurological function.

## Abstract

Lhermitte–Duclos disease (LDD) is a rare dysplastic cerebellar gangliocytoma often associated with Cowden syndrome and phosphatase and tensin homolog (PTEN) alterations. We report a three-case series focusing on imaging, histopathology, PTEN testing, surgical decision-making, and outcomes.

We retrospectively identified three adults with LDD who underwent standardized preoperative imaging [including magnetic resonance spectroscopy (MRS) and perfusion when feasible], surgery, and structured follow-up with Karnofsky Performance Status (KPS). PTEN assessment included immunohistochemistry and/or genetic testing where available.

All patients in this case series were women (18–53 years). Two underwent subtotal resection and one underwent gross total resection. Characteristic “tiger-striped” magnetic resonance imaging (MRI) appearance was present in all cases. Histopathology showed thickened molecular layer, loss of Purkinje cells, and hypertrophic ganglion-like neurons. One patient required unplanned posterior fossa decompression due to severe postoperative edema. At 6 months, two patients improved functionally while one had poor neurological outcome. PTEN testing supported the association with PTEN hamartoma tumor syndrome in one case.

PTEN evaluation should be considered in adults with LDD, especially when clinical features suggest Cowden syndrome. Surgical management should balance extent of resection with preservation of venous outflow and cerebellar function. Non-surgical strategies [observation, stereotactic radiotherapy, and exploratory mechanistic target of rapamycin (mTOR) inhibition] may be an option in selected scenarios.

This single-center retrospective series is limited by its small sample size and variable follow-up imaging.

## Linked entities

- **Genes:** PTEN (phosphatase and tensin homolog) [NCBI Gene 5728]
- **Diseases:** Lhermitte–Duclos disease (MONDO:0019002), Cowden syndrome (MONDO:0016063)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}
- **Diseases:** edema (MESH:D004487), Cowden syndrome (MESH:D006223)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12588853/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588853/full.md

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Source: https://tomesphere.com/paper/PMC12588853