Pheochromocytoma: A Rare Cause of Secondary Hypertension

Authors

DOI:

https://doi.org/10.22502/jlmc.v1i1.17

Keywords:

adrenal gland, pheochromocytoma, secondary hypertension

Abstract

 

Introduction: Pheochromocytoma is a rare tumor, originating from the chromaffin tissue. Its frequency is approximately 1/100,000. The clinical manifestation is due to catecholamine excess, which includes high blood pressure, palpitation, headache, sweating, nausea, vomiting, trembling, weakness, irritation, abdominal and chest pain, dyspnea, red warm face, constipation, polyuria, and polydipsia.

 

Case Report: We present a case of 53 years old male, hospitalized for hypertensive crisis following the manipulation of left sided frozen shoulder. He had labile blood pressure ranging from 220/120 systolic- 90/60 diastolic, profuse sweating and tachycardia. Findings of Contrast enhanced CT of abdomen was consistent with right adrenal pheochromocytoma and 24 hours urinary VMA was 17 mg /24 hr (Normal <13.6 mg /24hr). After the clinical, paraclinical investigations and radiological tests, it was proved to be a pheochromocytoma. The surgical intervention was planned. But due to unavailability of required antihypertensive drugs in Nepal (alpha-blockers like phentolamine and phenoxybenzamine), surgeons were reluctant to operate, although blood pressure was well controlled with use of sodium nitroprusside during hypertensive crisis and prazosin, a selective alpha blocker as maintainance therapy. The use of prazosin to control hypertension secondary to pheochromocytoma is limited to case report and case series.

 

Conclusion: Although rare, pheochromocytoma is a treatable surgical cause of secondary hypertension.

Downloads

Download data is not yet available.

Author Biographies

  • Sahadeb Prasad Dhungana, KIST Medical College
    Department of Medicine
  • G P Acharya, KIST Medical College
    Department of Medicine
  • R M Piryani, KIST Medical College
    Department of Medicine
  • S K Shrestha, KIST Medical College
    Department of Medicine

Additional Files

Published

2013-06-30

Issue

Section

Case Report

How to Cite

1.
Pheochromocytoma: A Rare Cause of Secondary Hypertension. J Lumbini Med Coll [Internet]. 2013 Jun. 30 [cited 2025 Sep. 14];1(1):48-50. Available from: https://www.jlmc.edu.np/index.php/JLMC/article/view/17

Most read articles by the same author(s)