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Scholars Journal of Medical Case Reports | Volume-11 | Issue-04
A Case of Clinically Silent Giant Right Pheochromocytoma
Ahmanna Hussein-Choukri, A. Diani, A. El Hajjami, B. Boutakioute, M. Ouali Idrissi, N. Cherif Idrissi El Guennouni, S. Chtioui, S. Rafi, G. H. El Mghari, N. El Ansari, R. Ait Ouali, M. A. Lakmichi, Z.
Published: April 9, 2023 | 278 106
DOI: 10.36347/sjmcr.2023.v11i04.005
Pages: 440-443
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Abstract
Patients with pheochromocytoma are typically symptomatic. Hypertension is the most common sign of pheochromocytoma. Clinically silent giant pheochromocytoma is a rare adrenal disease; complete resection is the only curative treatment. Due to the serious surgical risk, successful resection is very difficult. We report a case of 70-year-old- female with giant pheochromocytoma, which was successfully resected. There were no intraoperative and postoperative complications. We analyze and report our experience.