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

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...

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Autores principales: LU, Chirag, Naushad, Altaf A, R, Manjunath P, Kalra, Pramila, Selvan, Chitra, Y P, Ganavi, Kolla, Bharathi, Sourabh, Sagar, GN, Devamsh, S, Nikitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412895/
https://www.ncbi.nlm.nih.gov/pubmed/37575861
http://dx.doi.org/10.7759/cureus.41671
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author LU, Chirag
Naushad, Altaf A
R, Manjunath P
Kalra, Pramila
Selvan, Chitra
Y P, Ganavi
Kolla, Bharathi
Sourabh, Sagar
GN, Devamsh
S, Nikitha
author_facet LU, Chirag
Naushad, Altaf A
R, Manjunath P
Kalra, Pramila
Selvan, Chitra
Y P, Ganavi
Kolla, Bharathi
Sourabh, Sagar
GN, Devamsh
S, Nikitha
author_sort LU, Chirag
collection PubMed
description 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.
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spelling pubmed-104128952023-08-11 Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India LU, Chirag Naushad, Altaf A R, Manjunath P Kalra, Pramila Selvan, Chitra Y P, Ganavi Kolla, Bharathi Sourabh, Sagar GN, Devamsh S, Nikitha Cureus Endocrinology/Diabetes/Metabolism 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. Cureus 2023-07-10 /pmc/articles/PMC10412895/ /pubmed/37575861 http://dx.doi.org/10.7759/cureus.41671 Text en Copyright © 2023, LU et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Endocrinology/Diabetes/Metabolism
LU, Chirag
Naushad, Altaf A
R, Manjunath P
Kalra, Pramila
Selvan, Chitra
Y P, Ganavi
Kolla, Bharathi
Sourabh, Sagar
GN, Devamsh
S, Nikitha
Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title_full Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title_fullStr Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title_full_unstemmed Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title_short Pheochromocytoma: Clinical Experience From a Single Tertiary Care Center in India
title_sort pheochromocytoma: clinical experience from a single tertiary care center in india
topic Endocrinology/Diabetes/Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412895/
https://www.ncbi.nlm.nih.gov/pubmed/37575861
http://dx.doi.org/10.7759/cureus.41671
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