# Stereotactic Body Radiation Therapy in the Management of Recurrent Unresectable Retroperitoneal Ganglioneuroma

**Authors:** Bradley Callas, Shyam Jani, Isheeta S Govardhan, Nitika Thawani, Shyamal Patel

PMC · DOI: 10.7759/cureus.102628 · Cureus · 2026-01-30

## TL;DR

A rare case of a non-surgical treatment using radiation therapy successfully managed a recurring ganglioneuroma tumor in a patient.

## Contribution

First reported use of stereotactic body radiotherapy for a retroperitoneal ganglioneuroma.

## Key findings

- SBRT was well-tolerated with no significant toxicity in the patient.
- Two-year follow-up showed stable disease without tumor progression.
- SBRT may be a viable treatment option when surgery is not possible.

## Abstract

Ganglioneuromas are rare, benign tumors arising from neural crest cells, typically managed with surgical resection. We present a unique case of a 35-year-old man with a history of ganglioneuroma resected in early childhood, who developed a recurrent retroperitoneal mass more than 30 years later. Imaging revealed a 12 cm lesion encasing critical structures, rendering it surgically unresectable. The patient underwent stereotactic body radiotherapy (SBRT), receiving 40 Gy in five fractions using volumetric modulated arc therapy (VMAT). Treatment was well-tolerated with no significant toxicity. Follow-up imaging over two years demonstrated stable disease without progression or symptom recurrence. To our knowledge, this is the first reported case of SBRT utilized for a retroperitoneal ganglioneuroma, highlighting its potential as a noninvasive alternative in cases where surgery is contraindicated. This case underscores the importance of long-term surveillance in patients with previously resected ganglioneuromas and suggests that SBRT may be a viable treatment option when surgical intervention poses significant risks.

## Linked entities

- **Diseases:** ganglioneuroma (MONDO:0005033)

## Full-text entities

- **Genes:** PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** psoriasis (MESH:D011565), Ganglioneuromas (MESH:D005729), spinal cord compression (MESH:D013117), vomiting (MESH:D014839), abdominal bloating (MESH:D000007), benign neoplasms (MESH:D009369), neural crest-derived tumors (MESH:C536408), hydronephrosis (MESH:D006869), SBO (MESH:D007409), abdominal pain (MESH:D015746), toxicity (MESH:D064420), metastases (MESH:D009362)
- **Chemicals:** catecholamines (MESH:D002395), MAG3 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12950179/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950179/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950179/full.md

---
Source: https://tomesphere.com/paper/PMC12950179