Best Doctor for Pheochromocytoma Treatment in Ahmedabad

Dr. SK Agarwal is renowned as the premier doctor for Pheochromocytoma, offering unparalleled expertise and compassionate care. With a deep understanding of the condition and a patient-centric approach, he delivers the best-in-class treatment, empowering patients to lead healthy and fulfilling lives.

  • 25 years of experience in Pheochromocytoma treatment.
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Pheochromocytoma Treatment in Ahmedabad

Pheochromocytoma is a rare tumor that develops in the adrenal glands, which are located on top of the kidneys. These tumors arise from chromaffin cells, which are responsible for producing adrenaline and noradrenaline (also known as epinephrine and norepinephrine, respectively). Pheochromocytomas can occur at any age but are most commonly diagnosed between the ages of 30 and 50.

The exact cause of pheochromocytoma is often unknown, but it can be associated with certain inherited genetic mutations, such as those found in multiple endocrine neoplasia type 2 (MEN2), von Hippel-Lindau disease, or neurofibromatosis type 1. In some cases, pheochromocytomas may be part of a condition called paraganglioma-pheochromocytoma syndrome.

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Frequently Asked Questions

Pheochromocytoma is considered a rare tumor. The exact prevalence is difficult to determine, but it is estimated to occur in approximately 2 to 8 per million individuals per year.

While the majority of pheochromocytomas occur sporadically without a clear cause, certain genetic conditions increase the risk. These include multiple endocrine neoplasia type 2 (MEN2), von Hippel-Lindau (VHL) disease, neurofibromatosis type 1 (NF1), and paraganglioma-pheochromocytoma syndrome.

Pheochromocytomas can occur at any age, but they are most commonly diagnosed between the ages of 30 and 50. However, they can also be found in children and older adults.