A Case of a 20-year-old male with recurrent pheochromocytoma / [author]: Llorin, Alexandra Kathryn I.
Language: English Publication details: Fairview, Quezon City: Department od Internal Medicine, FEU-NRMF, 2024Description: (in folder) with flash drive (soft copy)Content type:- text
- unmediated
- volume
- MED 2024 0004
Item type | Current library | Call number | Status | Date due | Barcode | |
---|---|---|---|---|---|---|
Room Use | Far Eastern University - Nicanor Reyes Medical Foundation | MED 2024 0004 (Browse shelf(Opens below)) | Available | R000771 |
Includes bibliographical references.
ABSTRACT: The recurrence of a pheochromocytoma is a rare medical phenomenon characterized by the reappearance of a previously treated or previously detected tumor originating from the adrenal medulla or extra-adrenal chromaffin tissue. These tumors give rise to an overproduction of catecholamines, causing severe and unpredictable episodic hypertension. The recurrence of this condition presents unique challenges to both patients and healthcare providers, as it demands comprehensive evaluation, precise diagnostic approaches, and tailored treatment strategies. Understanding the intricacies of recurrent pheochromocytoma is crucial for guiding further research and optimizing patient care in the pursuit of improved long-term prognosis and management of this rare medical entity. OBJECTIVES: 1. To present a case of a 20-year-old male who was diagnosed with recurrent pheochromocytoma 2. To discuss the approach to diagnosis and management of pheochromocytoma and its recurrence.
Research - Department of Medicine
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