Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India.

Autor:	Lu C; Endocrinology, Ramaiah Medical College, Bangalore, IND., Naushad AA; Endocrinology, Ramaiah Medical College, Bangalore, IND., R MP; Endocrinology, Ramaiah Medical College, Bangalore, IND., Kalra P; Endocrinology, Ramaiah Medical College, Bangalore, IND., Selvan C; Endocrinology, Ramaiah Medical College, Bangalore, IND., Y P G; Endocrinology, Ramaiah Medical College, Bangalore, IND., Kolla B; Endocrinology, Ramaiah Medical College, Bangalore, IND., Sourabh S; Endocrinology, Ramaiah Medical College, Bangalore, IND., Gn D; Gastroenterology, St. Johns Medical College, Bangalore, IND., S N; Endocrinology, Ramaiah Medical College, Bangalore, IND.
Jazyk:	angličtina
Zdroj:	Cureus [Cureus] 2023 Jul 10; Vol. 15 (7), pp. e41671. Date of Electronic Publication: 2023 Jul 10 (Print Publication: 2023).
DOI:	10.7759/cureus.41671
Abstrakt:	Introduction: Pheochromocytoma is a catecholamine-secreting tumor arising from adrenomedullary chromaffin cells that has a varied clinical presentation. Identification of this tumor, which has episodic symptoms, is a diagnostic challenge for clinicians. Diagnosis at an appropriate time is important because it is associated with significant morbidity and mortality. This study aims to mitigate the limited availability of data in our geographical area. Aims and Objectives: To assess the clinical, biochemical, and radiological features and outcomes of patients diagnosed with pheochromocytoma at our center. Materials and Methods: This is a retrospective study. Patients diagnosed with pheochromocytoma during 2015-2023 were included in the study. Clinical, biochemical, and radiological data were collected at presentation, post-surgery, discharge, and until the last follow-up; data were retrieved from hospital records. Statistical analysis was done using IBM Corp. Released 2011. IBM SPSS Statistics for Windows, Version 20.0. Armonk, NY: IBM Corp. Results: This study included 19 patients, of whom 10 (52.6%) were female. The most common clinical presentation was a hypertensive crisis in patients with pre-existing hypertension (63.1%), followed by headache (47.3%). The classical triad of headache, palpitation, and sweating was seen in only three patients (15.7%). The mean tumor size was 5.01±2.06 cm, with a range of 2.5 to 12 cm. All patients underwent adrenalectomy; six patients (31.5%) had perioperative complications, with post-operative hypotension being the most common at 21% (n = 4), followed by an acute coronary event during alpha blockade in one patient (0.05%) and an intra-operative hypertensive crisis in one patient (5%). A biochemical remission rate post-surgery was achieved in 17 (89.47%) patients. Conclusions: Hypertensive crisis in patients with pre-existing hypertension was the predominant presenting feature in most of our patients. Female predominance was noted (52.3%) compared to males. Perioperative complications were observed in 31.5% of patients, with post-operative hypotension being the most common complication. Competing Interests: The authors have declared that no competing interests exist. (Copyright © 2023, LU et al.)
Databáze:	MEDLINE
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