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Ganglioneuroma is a tumor of the peripheral nervous system.
Causes, incidence, and risk factors
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.
There are no known risk factors. However, the tumors may be associated with some genetic problems, such as neurofibromatosis type 1.
A ganglioneuroma usually causes no symptoms, and is only discovered when being examined or treated for another condition.
Symptoms depend on the location of the tumor and the type of chemicals released.
If the tumor is in the chest area (mediastinum), symptoms may include:
If the tumor is lower down in the abdomen in the area called the retroperitoneal space, symptoms may include:
If the tumor is near the spinal cord, it may cause:
Compression of the spinal cord, which leads to pain and loss of strength or feeling in the legs, the arms, or both
These tumors may produce certain hormones, which can cause the following symptoms:
Signs and tests
The best tools to identify a ganglioneuroma are:
Blood and urine tests may be done to determine if the tumor is producing hormones or other chemicals.
A biopsy or complete removal of the tumor may be needed to confirm the diagnosis.
Treatment involves surgery to remove the tumor (if it is causing symptoms).
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.
If the tumor has been present for a long time and has pressed on the spinal cord or caused other symptoms, surgery to remove the tumor may not necessarily reverse the damage.
Compression of the spinal cord may result in loss of movement (paralysis), especially if the cause is not detected promptly.
Surgery to remove the tumor may also lead to complications in some cases. However, rare, persistent problems due to compression may occur even after the tumor is removed.
Calling your health care provider
Call your health care provider if you or your child has symptoms that may be caused by this type of tumor.
McCool FD. Diseases of the diaphragm, chest wall, pleura, and mediastinum. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 99.
- Last reviewed on 8/29/2012
- David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; Luc Jasmin, MD, PhD, Department of Neurosurgery at Cedars-Sinai Medical Center, Los Angeles, and Department of Anatomy at UCSF, San Francisco, CA. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M. Health Solutions, Ebix, Inc.
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This page was last updated: May 20, 2014