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Hereditary Paraganglioma-Pheochromocytoma (PGL/PCC)

Hereditary paraganglioma-pheochromocytoma (PGL/PCC), also known as familial paraganglioma-pheochromocytoma syndrome, is a rare genetic condition that increases the risk of developing certain types of cancer, most notably paragangliomas and pheochromocytomas. Paragangliomas and pheochromocytomas are classified as neuroendocrine tumours (NETs).

NETS are a complex group of tumours that develop in the neuroendocrine system, which is responsible for regulating important bodily functions such as heart rate, blood pressure and metabolism. They most commonly develop in the gastro-intestinal tract, pancreas, and the lungs; however, they can develop anywhere in the body. These tumours develop from neuroendocrine cells, which are responsible for receiving signals from the nervous system and producing hormones and peptides (small proteins) in response.

Familial cancer syndromes, also known as hereditary cancer syndromes, are rare conditions that cause an increased risk of cancer as the result of inherited genetic mutations in certain cancer-related genes. They can affect both adults and children, however they generally develop in people at a younger age than normal. While familial cancer syndromes are not classified as cancer, they are equally as severe and can be life-threatening as they are associated with the development of various tumours throughout the body. Having a familial cancer syndrome does not guarantee the development of cancer, however the risk of developing cancer is higher than those who do not have a familial cancer syndrome.

PGL/PCC tends to affect the sexes equally, and is often diagnosed in childhood. However, anyone can develop this disease.

PGL/PCC is most commonly associated with the development of paragangliomas and pheochromocytomas, however it has also been linked to other types of tumours. Some examples include:

Treatment

When cancers are detected, they are staged and graded based on size, metastasis, and how the cancer cells look under the microscope. Staging and grading helps your doctors determine the best treatment for you. However, each patient with PGL/PCC will present with a unique disease behaviour, with varying tumour locations and symptoms. As such, there is no one treatment method that will work for everyone, and there is no standard staging system for this disease. Instead of staging and grading, your doctor will recommend a treatment plan based on the following factors:

  • Type of tumours present.
  • Whether the tumours are malignant (cancerous) or benign (non-cancerous).
  • Tumour location.
  • Whether or not malignant tumours have metastasised.
  • Your age.
  • General health.
  • Your treatment preferences.

Your doctor may also recommend genetic testing, which analyses your tumour DNA and can help determine which treatment has the greatest chance of success. They will then discuss the most appropriate treatment option for you.

Treatment options for tumours associated with PGL/PCC may include:

  • Surgery to remove as much of the tumour(s) as possible – these will vary based on tumour type and location.
  • Chemotherapy.
  • Radiation therapy.
  • Watch and wait.
  • Clinical trials.
  • Palliative care.

Cancer Screening

Once a diagnosis of PGL/PCC has been confirmed, implementing a targeted screening plan becomes essential due to the increased risk of developing certain cancers.  The content of this plan will vary from person to person based on the genetic mutation involved, your family’s history of cancer and the types of cancers that may be present. It will also outline the routine tests you should have and how regularly you should have them.  Some recommendations for PGL/PCC may include:

  • Annual physical examination.
  • Serum or urine metanephrine tests every 1-2 years in children, then annually in adults.
  • Whole body MRI every 2-3 years.

Screening options for PGL/PCC may evolve as new technologies are developed and our understanding of the condition grows. It is essential to discuss your individual circumstances with your healthcare team to determine the most appropriate screening plan for you.

Risk factors

In most cases, PGL/PCC is caused by genetic mutations of succinate dehydrogenase (SDH) genes, however other genes can also cause the disease. Some examples include:

  • SDHA (succinate dehydrogenase complex flavoprotein subunit A, tumour suppressor gene).
  • SDHB (succinate dehydrogenase complex iron-sulphur subunit B, tumour suppressor gene).
  • SDHC (succinate dehydrogenase complex subunit C, tumour suppressor gene).
  • SDHD (succinate dehydrogenase complex subunit D, tumour suppressor gene).
  • SDHAF2 (succinate dehydrogenase complex assembly factor two, tumour suppressor gene).
  • MAX (MYC-associated factor X, tumour suppressor gene).
  • TMEM127 (transmembrane protein 127, tumour suppressor gene).

PGL/PCC is an autosomal dominant disease, which means that you have a 50% chance of developing the condition if one of your parents carries the genetic mutation.

Symptoms

The symptoms of PGL/PCC often vary by the type(s) of tumours present. General symptoms of PGL/PCC may include:

  • Hypertension.
  • Headaches.
  • Heart palpitations.
  • Unexplainable sweating.
  • Tachycardia.
  • Anxiety.
  • Being very pale.
  • Nausea and/or vomiting.
  • Unexplainable weight loss/loss of appetite.
  • Abdominal pain and/or mass.
  • Blood in stool and/or vomit.
  • Fatigue.
  • Difficulties swallowing.

Symptoms related to specific tumours can be found on our knowledgebase.

Not everyone with the symptoms above will have cancer, but see your general practitioner (GP) if you are concerned.

Diagnosis

If your doctor suspects you have tumours associated with PGL/PCC, they may order some of the following tests to confirm the diagnosis and refer you to a specialist for treatment. The tests required for diagnosis will often vary based on the symptoms present, and where the tumour(s) are suspected to be located.

  • Physical examination.
  • Genetic testing.
  • Endocrine studies.
  • Imaging tests, potentially including:
    • MRI (magnetic resonance imaging).
    • CT (computed tomography) scan.
    • PET (positron emission tomography) scan.
    • MIBG scan.
    • Ultrasound.
  • Exploratory procedures, such as an endoscopy.
  • Biopsy.

References

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