Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report
Abstract Background Pheochromocytoma is well-known for sudden initial presentations, particularly in younger patients. Hemodynamic instability may cause serious complications and delay a patient’s ability to undergo surgical resection. Larger tumors present a further challenge because of the risk of...
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doaj-487e04f25c9f45b9bc86016fb68414012020-11-25T04:12:26ZengBMCBMC Urology1471-24902019-11-011911610.1186/s12894-019-0554-5Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case reportUmberto Maestroni0Francesco Ziglioli1Marco Baciarello2Valentina Bellini3Raffaele Dalla Valle4Simona Cataldo5Giada Maspero6Elena Bignami7Department. of General and Specialty Surgery, Urology Unit, University Hospital of ParmaDepartment. of General and Specialty Surgery, Urology Unit, University Hospital of ParmaDepartment of Medicine and Surgery, Anesthesia, Critical Care and Pain Medicine, University of ParmaDepartment of Medicine and Surgery, Anesthesia, Critical Care and Pain Medicine, University of ParmaDepartment of Medicine and Surgery, Hepatobiliary Surgery Unit, University of ParmaDepartment of Medicine, Endocrinology and Metabolic Diseases Unit, University Hospital of ParmaDepartment of Medicine and Surgery, Anesthesia, Critical Care and Pain Medicine, University of ParmaDepartment of Medicine and Surgery, Anesthesia, Critical Care and Pain Medicine, University of ParmaAbstract Background Pheochromocytoma is well-known for sudden initial presentations, particularly in younger patients. Hemodynamic instability may cause serious complications and delay a patient’s ability to undergo surgical resection. Larger tumors present a further challenge because of the risk of catecholamine release during manipulations. In the case we present, increases in systemic vascular resistance caused cardiogenic shock, and the size of the lesion prompted surgeons to veer off from their usual approach. Case presentation A 38-year-old female patient was admitted to our intensive care unit with hypertension and later cardiogenic shock. Profound systolic dysfunction (left ventricular ejection fraction of 0.12) was noted together with severely increased systemic vascular resistance, and gradually responded to vasodilator infusion. A left-sided 11-cm adrenal mass was found with computed tomography and confirmed a pheochromocytoma with a meta-iodo-benzyl-guanidine scintigraphy. Surgical treatment was carefully planned by the endocrinologist, anesthesiologist and surgeon, and was ultimately successful. After prolonged hemodynamic stabilization, open adrenalectomy and nephrectomy were deemed safer because of lesion size and the apparent invasion of the kidney. Surgery was successful and the patient was discharged home 5 days after surgery. She is free from disease at almost 2 years from the initial event. Conclusions Large, invasive pheochromocytoma can be safely and effectively managed with open resection in experienced hands, provided all efforts are made to achieve hemodynamic stabilization and to minimize. Catecholamine release before and during surgery.http://link.springer.com/article/10.1186/s12894-019-0554-5PheochromocytomaAdrenalectomyCardiogenic shockCase report |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Umberto Maestroni Francesco Ziglioli Marco Baciarello Valentina Bellini Raffaele Dalla Valle Simona Cataldo Giada Maspero Elena Bignami |
spellingShingle |
Umberto Maestroni Francesco Ziglioli Marco Baciarello Valentina Bellini Raffaele Dalla Valle Simona Cataldo Giada Maspero Elena Bignami Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report BMC Urology Pheochromocytoma Adrenalectomy Cardiogenic shock Case report |
author_facet |
Umberto Maestroni Francesco Ziglioli Marco Baciarello Valentina Bellini Raffaele Dalla Valle Simona Cataldo Giada Maspero Elena Bignami |
author_sort |
Umberto Maestroni |
title |
Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
title_short |
Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
title_full |
Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
title_fullStr |
Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
title_full_unstemmed |
Multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
title_sort |
multidisciplinary management of a large pheochromocytoma presenting with cardiogenic shock: a case report |
publisher |
BMC |
series |
BMC Urology |
issn |
1471-2490 |
publishDate |
2019-11-01 |
description |
Abstract Background Pheochromocytoma is well-known for sudden initial presentations, particularly in younger patients. Hemodynamic instability may cause serious complications and delay a patient’s ability to undergo surgical resection. Larger tumors present a further challenge because of the risk of catecholamine release during manipulations. In the case we present, increases in systemic vascular resistance caused cardiogenic shock, and the size of the lesion prompted surgeons to veer off from their usual approach. Case presentation A 38-year-old female patient was admitted to our intensive care unit with hypertension and later cardiogenic shock. Profound systolic dysfunction (left ventricular ejection fraction of 0.12) was noted together with severely increased systemic vascular resistance, and gradually responded to vasodilator infusion. A left-sided 11-cm adrenal mass was found with computed tomography and confirmed a pheochromocytoma with a meta-iodo-benzyl-guanidine scintigraphy. Surgical treatment was carefully planned by the endocrinologist, anesthesiologist and surgeon, and was ultimately successful. After prolonged hemodynamic stabilization, open adrenalectomy and nephrectomy were deemed safer because of lesion size and the apparent invasion of the kidney. Surgery was successful and the patient was discharged home 5 days after surgery. She is free from disease at almost 2 years from the initial event. Conclusions Large, invasive pheochromocytoma can be safely and effectively managed with open resection in experienced hands, provided all efforts are made to achieve hemodynamic stabilization and to minimize. Catecholamine release before and during surgery. |
topic |
Pheochromocytoma Adrenalectomy Cardiogenic shock Case report |
url |
http://link.springer.com/article/10.1186/s12894-019-0554-5 |
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