Paraganglioma Pheochromocytoma | Symptoms & Causes
What are the symptoms of paraganglioma/pheochromocytoma?
The symptoms of paraganglioma/pheochromocytoma (PCCs and PGLs) may vary from child to child and depend on where the tumor is located and whether it produces hormones. Symptoms might mimic other, more common ailments.
For PCCs/PGLs, the most common symptoms are:
- high blood pressure
- rapid pulse
- heart palpitations
- headache
- dizziness
- poor weight gain despite good appetite
- abdominal pain
- nausea
- vomiting
- pale skin
- clammy skin
- sweating
- growth failure
Because many of these symptoms can also point to other conditions, it’s important to have your child diagnosed by a qualified medical professional right away.
What causes PCCs/PGLs?
Sometimes, tumors emerge with no known cause. Some result from a mix of genetic and environmental factors, while others are linked to inherited conditions.
Examples of conditions associated with PGLs and PCCs include hereditary paraganglioma-pheochromocytoma syndrome, neurofibromatosis, von Hippel-Lindau disease, multiple endocrine neoplasia syndromes, tuberous sclerosis, Sturge-Weber syndrome, and ataxia-telangiectasia.
Paraganglioma Pheochromocytoma | Diagnosis & Treatments
How are paraganglioma/pheochromocytoma diagnosed?
The first step in treating your child is forming an accurate and complete diagnosis. Your child’s physician may order a number of different tests including:
- physical exam and complete medical history.
- blood and urine tests.
- biopsy
- magnetic resonance imaging (MRI)
- computerized tomography scan (CT/CAT scan)
- molecular testing to determine whether the tumor is linked to specific genes
There may be other diagnostic tests that your doctor will discuss with you depending on your child's individual situation. After we complete all necessary tests, our experts meet to review and discuss what they have learned about your child's condition. Then, we will meet with you and your family to discuss the results and outline the best possible treatment options.
What are the treatment options for paraganglioma/pheochromocytoma?
Treatment for paraganglioma or pheochromocytoma will depend on the location and type of your child’s tumor. Your child's doctor may recommend surgery including a biopsy, laparoscopy or thoracoscopy. Sometimes before removing a pheochromocytoma, your child’s physician may prescribe medicine to control high blood pressure. There are also some newer agents that are being investigated to reduce the need for big surgeries for advanced paragangliomas.