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Report of two cases of adrenal Pheochromocytoma
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H Shafi *   , A Ali Ramaji , YR Yousef Nia |
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Abstract: (8082 Views) |
| Background and Objective: Less than 1% of pheochromocytoma account for hypertensive vascular diseases. The goal of this report is early diagnosis of this tumor since it is surgically treatable and preventive for lethal complication. In this study, two cases of patients with hypertension due to adrenal pheochromocytoma who were treated by surgical adrenalectomy were reported. Cases: The first patient was a 45-year-old female who presented with hypertension, headache, abdominal pain, sweating weight loss and diabetic mellitus. An 8×6 cm² mass was reported in her left adrenal by CT scan. She was operated adrenalectomy. She immediately got a normal blood pressure and controlled diabetic mellitus. The second patient was a 61-year-old male who presented with hypertension and elevated level of 24-hour urinary catecholamine. He was surgically treated by adrenalectomy of right adrenal pheochromocytoma after a 7×6 cm² mass was detected on CT scan in his right adrenal as the same of first patient, he got a normal blood pressure and controlled diabetic mellitus immediately after operation. Conclusion: Although pheochromocytoma is a rare cause of elevation of arterial pressure it should be always considered as a cause of elevation of blood pressure. So after the diagnosis it was recommended administration of phenoxybenzamine as an irreversible α blocker, to prevent hypertensive crisis and cardiac arrhythmia, and for symptom relief of the patients before, during and after the operation, respectively. |
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| Keywords: Pheochromocytoma, Adrenal gland, Elevation of blood pressure |
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Full-Text [PDF 228 kb]
(5338 Downloads)
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Type of Study: Research |
Subject:
Biochemical
Accepted: 2014/05/31 | Published: 2014/05/31
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