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Bilateral pheochromcytomas presenting as shock: A rare case report
Pheochromocytomas are rare chromaffin cell tumors of adrenal medulla (90%) that secrete catecholamines. Among children, the average age of presentation is 11–13 years, with a male preponderance of 2:1. Symptoms may be caused by catecholamine overproduction, local pressure, or metastasis. Sustained h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067193/ https://www.ncbi.nlm.nih.gov/pubmed/35516716 http://dx.doi.org/10.4103/jfmpc.jfmpc_1251_21 |
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author | Pandya, Radhika H. Barad, Hardev V. Raghunandan, G. C. Trivedi, Bhadra Y. |
author_facet | Pandya, Radhika H. Barad, Hardev V. Raghunandan, G. C. Trivedi, Bhadra Y. |
author_sort | Pandya, Radhika H. |
collection | PubMed |
description | Pheochromocytomas are rare chromaffin cell tumors of adrenal medulla (90%) that secrete catecholamines. Among children, the average age of presentation is 11–13 years, with a male preponderance of 2:1. Symptoms may be caused by catecholamine overproduction, local pressure, or metastasis. Sustained hypertension is the most common symptom. Elevated circulating catecholamines can cause cardiovascular alterations such as coronary vasospasm, ventricular and supraventricular arrhythmias, and dilated cardiomyopathy, precipitating in cardiogenic shock. We present a rare case of cardiogenic shock as the initial presentation of a bilateral pheochromocytoma in a child. |
format | Online Article Text |
id | pubmed-9067193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-90671932022-05-04 Bilateral pheochromcytomas presenting as shock: A rare case report Pandya, Radhika H. Barad, Hardev V. Raghunandan, G. C. Trivedi, Bhadra Y. J Family Med Prim Care Case Report Pheochromocytomas are rare chromaffin cell tumors of adrenal medulla (90%) that secrete catecholamines. Among children, the average age of presentation is 11–13 years, with a male preponderance of 2:1. Symptoms may be caused by catecholamine overproduction, local pressure, or metastasis. Sustained hypertension is the most common symptom. Elevated circulating catecholamines can cause cardiovascular alterations such as coronary vasospasm, ventricular and supraventricular arrhythmias, and dilated cardiomyopathy, precipitating in cardiogenic shock. We present a rare case of cardiogenic shock as the initial presentation of a bilateral pheochromocytoma in a child. Wolters Kluwer - Medknow 2022-04 2022-03-18 /pmc/articles/PMC9067193/ /pubmed/35516716 http://dx.doi.org/10.4103/jfmpc.jfmpc_1251_21 Text en Copyright: © 2022 Journal of Family Medicine and Primary Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Pandya, Radhika H. Barad, Hardev V. Raghunandan, G. C. Trivedi, Bhadra Y. Bilateral pheochromcytomas presenting as shock: A rare case report |
title | Bilateral pheochromcytomas presenting as shock: A rare case report |
title_full | Bilateral pheochromcytomas presenting as shock: A rare case report |
title_fullStr | Bilateral pheochromcytomas presenting as shock: A rare case report |
title_full_unstemmed | Bilateral pheochromcytomas presenting as shock: A rare case report |
title_short | Bilateral pheochromcytomas presenting as shock: A rare case report |
title_sort | bilateral pheochromcytomas presenting as shock: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067193/ https://www.ncbi.nlm.nih.gov/pubmed/35516716 http://dx.doi.org/10.4103/jfmpc.jfmpc_1251_21 |
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