Ganglioneuromas are fully differentiated neuronal tumours that do not contain immature elements and potentially occur anywhere along the peripheral autonomic ganglion sites.
On imaging usually they present as well defined solid masses and can be quite large at presentation, generally they are hypoattenuating to muscle on CT and have a heterogeneous intermediate signal on both T1 and T2-weighted MRI sequences. Contrast enhancement ranges from none to heterogenous enhancement, calcification may be present in less than a quarter of cases.
Ganglioneuromas tend to occur in the paediatric population and are often asymptomatic. At the time of diagnosis, 60% of patients are under the age of 20 years 11. The median age at diagnosis is 7 years and there is a slight female predominance. This is in contrast to neuroblastoma which occurs in patients younger than 3 years old.
Ganglioneuromas are usually asymptomatic and often discovered incidentally as they are slow growing and usually endocrinologically inactive 11.
Like neuroblastomas and ganglioneuroblastomas, ganglioneuromas are derived from the primordial neural crest cells that form the sympathetic nervous system. Pathologically, they are composed of ganglion cells, schwann cells and fibrous tissue. They do not contain neuroblasts, intermediate cells, or mitotic figures and necrosis is not a feature12.
Ganglioneuromas most commonly arise in the paravertebral sympathetic chains of the posterior mediastinum (41.5%) or retroperitoneum (37.5%). Less common sites include the adrenal gland (21%) and neck (8%) 12. Paravertebral ganglioneuromas frequently extend through the neural foramina to involve the epidural space of the spinal canal 13. Intradural extramedullary ganglioneuromas have been reported but are extremely rare 10.
Ganglioneuromas may occur de novo or may arise from maturing neuroblastomas and ganglioneuroblastomas. They may also arise in neuroblastomas and ganglioneuroblastomas that have been treated with chemotherapy 12.
There are rare reports of metastatic ganglioneuromas. It is believed that these tumours represent metastases of neuroblastomas or ganglioneuroblastomas that have subsequently matured to ganglioneuromas. These patients have an excellent prognosis 12.
- multiple endocrine neoplasia type IIb 5-6: particularly with mucosal ganglioneuromas
Can potentially occur anywhere along the peripheral autonomic ganglion sites. The posterior paraspinal mediastinum one of the commonest locations (see paraspinal ganglioneuroma) 2 (~40%). Occurrence in retroperitoneum, neck and adrenal gland is also relatively common.
Lesions are generally well defined and can be quite large at presentation.
On paraspinal ganglioneuromas in particular, a posterior mediastinal mass may seen causing rib spreading and foraminal erosion. A retroperitoneal mass and scoliosis may also be present.
Typically seen as well-circumscribed, solid, encapsulated masses that are iso to hypoattenuating to muscle 8. The lesion may also demonstrate calcifications (~20% 2,4) which is typically fine and speckled, but may be coarse.
Ganglioneuromas are well circumscribed masses. They may appear encapsulated, although a true capsule is infrequent 12. Reported signal characteristics include:
- T1: tends to have homogeneously low or intermediate signal
- T2: tends to have heterogeneously intermediate or high signal
- T1 C+ (Gd): variable ranging from none to heterogenous enhancement
- ADC: ADC values tend to be higher to that of a neuroblastoma 9
Treatment and prognosis
Ganglioneuromas are typically slow growing tumours.
Treatment consists of complete surgical resection when possible. Complete resection ensures thorough sampling of the tumour, so that a confident diagnosis of ganglioneuroma can be made 12.
Prognosis is usually excellent, however local recurrence has been reported.
The differential depends on location; for thoracic lesions, consider the differential for a posterior mediastinal mass.
Differentials for paraspinal ganglioneuromas include:
- spinal neuroblastoma and ganglioneuroblastoma
- often cannot be differentiated from ganglioneuroma based on imaging characteristics
- metastases usually indicate neuroblastoma or ganglioneuroblastoma
- compared with ganglioneuromas, tumour calcification in neuroblastomas is more common (80-90%) and often amorphous and of a rough pattern
- spinal schwannoma and neurofibroma
- centred on neural foramen
- primarily seen in middle-aged adults
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- 7. Cai J, Zeng Y, Zheng H et-al. Retroperitoneal ganglioneuroma in children: CT and MRI features with histologic correlation. Eur J Radiol. 2010;75 (3): 315-20. doi:10.1016/j.ejrad.2010.05.040 - Pubmed citation
- 8. Ichikawa T, Ohtomo K, Araki T et-al. Ganglioneuroma: computed tomography and magnetic resonance features. Br J Radiol. 1996;69 (818): 114-21. doi:10.1259/0007-1285-69-818-114 - Pubmed citation
- 9. Gahr N, Darge K, Hahn G et-al. Diffusion-weighted MRI for differentiation of neuroblastoma and ganglioneuroblastoma/ganglioneuroma. 2010;doi:10.1016/j.ejrad.2010.04.005 - Pubmed citation
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- 12. Lonergan GJ, Schwab CM, Suarez ES et-al. Neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: radiologic-pathologic correlation. Radiographics. 2002;22 (4): 911-34. Radiographics (full text) - Pubmed citation
- 13. Brant WE, Helms CA. Fundamentals of Diagnostic Radiology. Lippincott Williams & Wilkins. (2007) ISBN:0781761352. Read it at Google Books - Find it at Amazon
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