A multidisciplinary approach of a patient with pheochromocytoma presenting as recurrent acute fulminant myocarditis: A rare case report and comprehensive review of literature.

Autor: Martha JW; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia. Electronic address: jwmartha@gmail.com., Prameswari HS; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia., Munita FF; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia., Kusumawardhani NY; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia; Department of Internal Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Bandung, West Java, Indonesia., Hasan M; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia., Astuti A; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia., Mulyani NN; Department of Internal Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Bandung, West Java, Indonesia., Agustina H; Department of Pathological Anatomy, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Bandung, West Java, Indonesia., Sari MT; Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University-Dr Hasan Sadikin Hospital, Jalan Prof Eyckman 38, Bandung, West Java 40161, Indonesia.
Jazyk: angličtina
Zdroj: Current problems in cardiology [Curr Probl Cardiol] 2024 Jun; Vol. 49 (6), pp. 102521. Date of Electronic Publication: 2024 Mar 16.
DOI: 10.1016/j.cpcardiol.2024.102521
Abstrakt: Fulminant myocarditis (FM) is a rare illness characterized by abrupt and severe widespread cardiac inflammation, which frequently results in mortality due to cardiogenic shock, ventricular arrhythmias, or multiorgan system failure. Pheochromocytoma is an uncommon and difficult-to-diagnose cause of FM, and it is associated with a significant risk of recurrent acute myocarditis. There is, however, little information on reoccurring acute FM. Herein, we report a rare case of recurrent acute FM due to pheochromocytoma. We present the case of a 22-year-old woman who was admitted to our hospital three days previously with acute dyspnea. Five months prior, the patient was diagnosed with post-acute myocarditis, and a massive tumor on the right adrenal gland was discovered, which lead to pheochromocytoma diagnosis. In this present admission, following the exclusion of infection, autoimmune, and metabolic derangements, pheochromocytoma was presumed to be the reason for the recurrence and more severe acute FM during the current hospitalization. The patient responded favorably to high-dose steroids combined with heart failure therapy regimens. To detect recurrent acute myocarditis related to pheochromocytoma, a multidisciplinary approach was used, including several laboratory biomarkers and imaging findings. Following pheochromocytoma removal and biopsy, the patient recovered satisfactorily. Our findings may provide beneficial contributions to the literature as pheochromocytoma is an uncommon but important cause of recurrent acute myocarditis. A multidisciplinary approach is essential in identifying acute FM and determining the underlying causes of this malady.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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