# Liponeurocytoma: Rare Neoplasm of the Central Nervous System

**Authors:** Zachary Sokol, Peter Parsells, Ravichandra Madineni

PMC · DOI: 10.7759/cureus.59221 · Cureus · 2024-04-28

## TL;DR

This case report describes a rare brain tumor called liponeurocytoma and the successful treatment of a patient through surgery.

## Contribution

The paper adds a new clinical case to the limited literature on liponeurocytoma, emphasizing successful surgical outcomes.

## Key findings

- A 46-year-old female was diagnosed with liponeurocytoma following surgical resection.
- The patient showed resolution of symptoms and remained neurologically intact two years post-surgery.

## Abstract

In this case report, we characterize an instance of diagnosis, treatment, characteristics, and outcomes of a patient with a liponeurocytoma, a rare WHO grade II brain tumor first described in 1978. This tumor has been described with a wide array of radiographic, microscopic, and histologic features, and there remains no consensus regarding the role of radiation therapy. Most patients have favorable outcomes after surgical resection. Here we present the case of a 46-year-old female who underwent suboccipital craniectomy for resection of a cerebellar mass, which was diagnosed as liponeurocytoma on final pathology. The patient experienced resolution of symptoms and is neurologically intact two years after resection of the tumor.

## Full-text entities

- **Diseases:** Neoplasm of the Central Nervous System (MESH:D016543), WHO grade II brain tumor (MESH:D001932), cerebellar mass (MESH:C536030), tumor (MESH:D009369)
- **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/PMC11132662/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC11132662/full.md

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Source: https://tomesphere.com/paper/PMC11132662