Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma
Background: Pheochromocytoma is a catecholamine secreting tumor that, in extremely rare cases, may develop over time from a non-functional adrenal adenoma. Catecholamine excess can lead to a kind of cardiomyopathy similar to that seen in tako-tsubo syndrome (TTS).Case report: A 69 years old female w...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-02-01
|
Series: | Frontiers in Endocrinology |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fendo.2020.00051/full |
_version_ | 1818039198085545984 |
---|---|
author | Pierpaolo Falcetta Francesca Orsolini Eleonora Molinaro Paolo Vitti Massimo Tonacchera |
author_facet | Pierpaolo Falcetta Francesca Orsolini Eleonora Molinaro Paolo Vitti Massimo Tonacchera |
author_sort | Pierpaolo Falcetta |
collection | DOAJ |
description | Background: Pheochromocytoma is a catecholamine secreting tumor that, in extremely rare cases, may develop over time from a non-functional adrenal adenoma. Catecholamine excess can lead to a kind of cardiomyopathy similar to that seen in tako-tsubo syndrome (TTS).Case report: A 69 years old female with a history of type 2 diabetes, hypertension, and a non-functional right adrenal adenoma diagnosed 3 years earlier was referred to our center for further investigations. During the evaluation, she had a hypertensive crisis with chest pain, tachycardia, and diaphoresis. Suspecting an acute coronary syndrome, she underwent coronary angiography, which showed the typical features of TTS. The high 24 h-urinary metanephrines excretion and abdominal MRI findings were suggestive of pheochromocytoma. Right laparoscopic adrenalectomy was performed, with the resolution of all symptoms. Pathology findings confirmed the diagnosis of pheochromocytoma. After 12 months, the patient was still asymptomatic, with the echocardiography displaying a complete recovery of the left-ventricular function.Conclusions: The development of a pheochromocytoma from an adrenal non functional adenoma is an extremely rare event, but potentially life-threating because of the catecholamine-associated cardiovascular toxicity. In particular, TTS is a form of cardiomyopathy that has been increasingly described as associated with catecholamine-secreting tumors. The exclusion of pheochromocytoma in a patient with TTS has important therapeutic implications, since the administration of β-blockers may be extremely harmful in patients with catecholamine surge in the absence of adequate α-blockage. |
first_indexed | 2024-12-10T07:54:49Z |
format | Article |
id | doaj.art-33851c52ea244f03a3bf80a8e5cf5762 |
institution | Directory Open Access Journal |
issn | 1664-2392 |
language | English |
last_indexed | 2024-12-10T07:54:49Z |
publishDate | 2020-02-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Endocrinology |
spelling | doaj.art-33851c52ea244f03a3bf80a8e5cf57622022-12-22T01:56:56ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922020-02-011110.3389/fendo.2020.00051501899Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal IncidentalomaPierpaolo FalcettaFrancesca OrsoliniEleonora MolinaroPaolo VittiMassimo TonaccheraBackground: Pheochromocytoma is a catecholamine secreting tumor that, in extremely rare cases, may develop over time from a non-functional adrenal adenoma. Catecholamine excess can lead to a kind of cardiomyopathy similar to that seen in tako-tsubo syndrome (TTS).Case report: A 69 years old female with a history of type 2 diabetes, hypertension, and a non-functional right adrenal adenoma diagnosed 3 years earlier was referred to our center for further investigations. During the evaluation, she had a hypertensive crisis with chest pain, tachycardia, and diaphoresis. Suspecting an acute coronary syndrome, she underwent coronary angiography, which showed the typical features of TTS. The high 24 h-urinary metanephrines excretion and abdominal MRI findings were suggestive of pheochromocytoma. Right laparoscopic adrenalectomy was performed, with the resolution of all symptoms. Pathology findings confirmed the diagnosis of pheochromocytoma. After 12 months, the patient was still asymptomatic, with the echocardiography displaying a complete recovery of the left-ventricular function.Conclusions: The development of a pheochromocytoma from an adrenal non functional adenoma is an extremely rare event, but potentially life-threating because of the catecholamine-associated cardiovascular toxicity. In particular, TTS is a form of cardiomyopathy that has been increasingly described as associated with catecholamine-secreting tumors. The exclusion of pheochromocytoma in a patient with TTS has important therapeutic implications, since the administration of β-blockers may be extremely harmful in patients with catecholamine surge in the absence of adequate α-blockage.https://www.frontiersin.org/article/10.3389/fendo.2020.00051/fulladrenal incidentalomapheochromocytomatako-tsubo syndromecatecholamineinfarctionventricular dysfunction |
spellingShingle | Pierpaolo Falcetta Francesca Orsolini Eleonora Molinaro Paolo Vitti Massimo Tonacchera Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma Frontiers in Endocrinology adrenal incidentaloma pheochromocytoma tako-tsubo syndrome catecholamine infarction ventricular dysfunction |
title | Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma |
title_full | Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma |
title_fullStr | Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma |
title_full_unstemmed | Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma |
title_short | Tako-tsubo Syndrome as First Manifestation in a Case of Pheochromocytoma Developed From a Non-functional Adrenal Incidentaloma |
title_sort | tako tsubo syndrome as first manifestation in a case of pheochromocytoma developed from a non functional adrenal incidentaloma |
topic | adrenal incidentaloma pheochromocytoma tako-tsubo syndrome catecholamine infarction ventricular dysfunction |
url | https://www.frontiersin.org/article/10.3389/fendo.2020.00051/full |
work_keys_str_mv | AT pierpaolofalcetta takotsubosyndromeasfirstmanifestationinacaseofpheochromocytomadevelopedfromanonfunctionaladrenalincidentaloma AT francescaorsolini takotsubosyndromeasfirstmanifestationinacaseofpheochromocytomadevelopedfromanonfunctionaladrenalincidentaloma AT eleonoramolinaro takotsubosyndromeasfirstmanifestationinacaseofpheochromocytomadevelopedfromanonfunctionaladrenalincidentaloma AT paolovitti takotsubosyndromeasfirstmanifestationinacaseofpheochromocytomadevelopedfromanonfunctionaladrenalincidentaloma AT massimotonacchera takotsubosyndromeasfirstmanifestationinacaseofpheochromocytomadevelopedfromanonfunctionaladrenalincidentaloma |