Ganglioneuroma: Difference between revisions
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Revision as of 01:25, 18 February 2025
Ganglioneuroma is a rare, benign neoplasm that originates from the ganglion cells of the autonomic nervous system. It is most commonly found in the adrenal gland, retroperitoneum, and posterior mediastinum.
Signs and Symptoms
The symptoms of ganglioneuroma can vary greatly depending on the location of the tumor. Some patients may be asymptomatic, while others may experience symptoms such as abdominal pain, hypertension, and diarrhea. In some cases, the tumor may cause hormonal imbalance leading to symptoms such as excessive sweating, rapid heart rate, and high blood pressure.
Diagnosis
The diagnosis of ganglioneuroma is often made incidentally during imaging studies for unrelated conditions. However, if a ganglioneuroma is suspected, a combination of imaging studies, laboratory tests, and biopsy may be used to confirm the diagnosis. Imaging studies such as CT scan and MRI can help identify the location and size of the tumor. Laboratory tests can help identify any hormonal imbalances caused by the tumor. A biopsy, where a small sample of the tumor is removed for examination under a microscope, can confirm the diagnosis.
Treatment
The treatment for ganglioneuroma typically involves surgical removal of the tumor. In some cases, if the tumor is small and not causing any symptoms, a watchful waiting approach may be taken. However, if the tumor is large, causing symptoms, or growing, surgical removal is usually recommended. In some cases, chemotherapy or radiation therapy may be used in addition to surgery.
Prognosis
The prognosis for ganglioneuroma is generally good, as the tumor is benign and does not typically spread to other parts of the body. However, the prognosis can vary depending on the size and location of the tumor, as well as the patient's overall health.


