Ganglioneuroma natural history
|
Ganglioneuroma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Ganglioneuroma natural history On the Web |
|
American Roentgen Ray Society Images of Ganglioneuroma natural history |
|
Risk calculators and risk factors for Ganglioneuroma natural history |
Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Natural History
- Ganglioneuromas are rare tumors that most frequently start in the autonomic nerve cells, which may be in any part of the body. The tumor are usually noncancerous (benign).
- Ganglioneuromas usually occur in people ages 10 to 40. They grow slowly, and may release certain chemicals or hormones.
Complications
Common complications of ganglioneuroma include:[1][2]
Common complications that can develop as a result of the surgical resection of ganglioneuroma include:[3]
Prognosis
Most ganglioneuromas are noncancerous. The expected outcome is usually good. A ganglioneuroma may, however, become cancerous and spread to other areas, or it may come back after removal.
References
- ↑ Leuthardt R, Petralli C, Lütschg J, von Schweinitz D, Kaiser G (2001). "Cortical blindness: an unusual complication after removal of a ganglioneuroma of the neck". Childs Nerv Syst. 17 (6): 356–8. PMID 11417417.
- ↑ Complications of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm
- ↑ Sánchez-Galán A, Barrena S, Vilanova-Sánchez A, Martín SH, Lopez-Fernandez S, García P; et al. (2014). "Ganglioneuroma: to operate or not to operate". Eur J Pediatr Surg. 24 (1): 25–30. doi:10.1055/s-0033-1358790. PMID 24327216.