Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/7109
Title: A Rare Case of Giant Malignant Pheochromocytoma
Authors: Younes, Ahmad
Ghattas, Souad
Semaan, Samar
Maalouf, Hani
Al Kadirri, Adham
Rahban, Hind
El Rassi, Ziad
Affiliations: Faculty of Medicine 
Keywords: Case report
Giant
Malignant
Pheochromocytoma
Issue Date: 2023-05-01
Part of: World Journal of Endocrine Surgery
Volume: 15
Issue: 2
Start page: 46
End page: 49
Abstract: 
A pheochromocytoma (PCC) is a tumor that arises from an embryonic neural crest and produces catecholamines at high levels. The mean size of these tumors is approximated to be around 7.2 cm, with an average weight of 222 g. In this case, a 61-year-old female patient was referred to our medical center to investigate multiple episodes of hypertensive crisis associated with a huge 18 cm right adrenal mass identified on a computed tomography (CT) scan and magnetic resonance imaging (MRI). Twenty-four-hour urine analysis and blood level exhibited elevated total metanephrine and normetanephrine levels. Mass resection was performed via laparotomy en bloc. Histopathological analysis of the resected specimen confirmed PCC of the right adrenal gland weighing 1900 g. The Adrenal gland Scaled Score (PASS) was 13. PCC may reach sizes much larger than the average observed in the literature and size tends to be positively correlated to malignancy.
URI: https://scholarhub.balamand.edu.lb/handle/uob/7109
ISSN: 09755039
DOI: 10.5005/jp-journals-10002-1450
Open URL: Link to full text
Type: Journal Article
Appears in Collections:Faculty of Medicine

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