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Pheochromocytoma

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What is Pheochromocytoma ?

Pheochromocytoma is a rare tumor of the adrenal gland that produces excess catecholamines, such as adrenaline and noradrenaline. This can cause:

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Symptoms

  • High blood pressure: Often severe and episodic.
  • Headaches: Severe and frequent.
  • Sweating: Excessive sweating, often accompanied by palpitations.
  • Palpitations: Rapid or irregular heartbeat.
  • Anxiety or panic attacks: Feeling anxious or panicky.

Diagnosis

  • Blood or urine tests: Measuring catecholamine levels.
  • Imaging tests: CT or MRI scans to locate the tumor.

Treatment

  • Surgery (adrenalectomy): Removing the affected adrenal gland.
  • Medications: To control blood pressure and symptoms before surgery.

Complications if left untreated

  • Severe hypertension: Can lead to cardiovascular disease.
  • Cardiac problems: Arrhythmias, heart failure.
  • Brain stroke

How is it diagnosed?

How is it diagnosed?
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Consult with experienced Doctors

MGMCH is home to some of the most eminent doctors in the world, most of whom are pioneers in their respective arenas and are renowned for developing
innovative and revolutionary procedures

  • Management Team
    Dr. Sapana Bothra Jain

    Professor & HOD

    Experience8years

    QualificationMBBS, MS (General surgery), MCh Endocrine and Breast Surgery (SGPGIMS Lucknow)

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