Adrenal pheochromocytoma as a rare cause of reversible left ventricular systolic dysfunction and malignant arrhythmias: a case series

. 2022 Mar ; 6 (3) : ytac098. [epub] 20220307

Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium electronic-ecollection

Typ dokumentu kazuistiky, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid35372755

BACKGROUND: Pheochromocytoma is a neuroendocrine tumour originating from the chromaffin cells of adrenal glands or sympathetic paraganglia. It produces most frequently norepinephrine, epinephrine, and dopamine. As a result of non-specific and variable clinical presentation, pheochromocytoma is difficult to diagnose. CASE SUMMARY: A 37-year-old female without medical history and 57-year-old male patient with diabetes, arterial hypertension, and aortic valve replacement with a mechanical prosthesis were admitted to the hospital after successful cardiopulmonary resuscitation due to ventricular fibrillation. In both patients, coronary angiography demonstrated a normal finding, and echocardiography showed left ventricular (LV) contractile dysfunction with improvement in the subsequent examination. In the first patient, the diagnosis of stress-induced cardiomyopathy was considered as the most probable cause. She was later admitted to hospital due to acute pulmonary oedema with hypertensive crisis. Echocardiography documented reversible LV systolic dysfunction with improvement after 3 days. The course of hospitalization of the male was complicated by multi-organ dysfunction syndrome comprising renal failure, paralytic ileus, and pancreatic irritation, which normalized after 2 weeks. The diagnosis of pheochromocytoma was confirmed by laboratory tests and imaging methods. After pharmacological pre-treatment with doxazosin in both patients and bisoprolol in the female, successful adrenalectomies were performed with no relapse of tumour. DISCUSSION: We describe an atypical clinical presentation of pheochromocytoma with initial cardiac arrest due to ventricular fibrillation and reversible LV systolic dysfunction. Our cases underline that clinical suspicion of pheochromocytoma as a potentially correctable cause should be raised in unexplained cases of severe heart failure, ventricular arrhythmias, and cardiac arrest.

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Harari A, Inabnet WB 3rd. Malignant pheochromocytoma: a review. Am J Surg 2011;201:700–708. PubMed

Zhang R, Gupta D, Albert SG.. Pheochromocytoma as a reversible cause of cardiomyopathy: analysis and review of the literature. Int J Cardiol 2017;249:319–323. PubMed

Björklund P, Backman S.. Epigenetics of pheochromocytoma and paraganglioma. Mol Cell Endocrinol 2018;469:92–97. PubMed

Tsirlin A, Oo Y, Sharma R, Kansara A, Gliwa A, Banerji MA.. Pheochromocytoma: a review. Maturitas 2014;77:229–238. PubMed

Gil-Barrionuevo E, Balibrea JM, Caubet E, Gonzalez O, Vilallonga R, Fort JM. et al. Adrenergic cardiomyopathy and cardiogenic shock as initial presentation of pheochromocytoma. A case report and review of the literature. Int J Surg Case Rep 2018;49:145–148. PubMed PMC

Chiu CC, Chen YC, Teng TH, Yang LH, Chen YP, Siao FY.. Sudden cardiac arrest after minor abdominal trauma: a successful resuscitation in a patient with haemorrhagic phaeochromocytoma. Resuscitation 2009;80:1323–1324. PubMed

Mita K, Tsugita K, Yasuda Y, Matsuki Y, Obata Y, Matsuki Y. et al. A successfully treated case of cardiac arrest after Caesarean section complicated by pheochromocytoma crisis and amniotic fluid embolism. J Anesth 2017;31:140–143. PubMed

Martucci VL, Pacak K.. Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment. Curr Probl Cancer 2014;38:7–41. PubMed PMC

Zografos GN, Vasiliadis G, Farfaras AN, Aggeli C, Digalakis M.. Laparoscopic surgery for malignant adrenal tumors. JSLS 2009;13:196–202. PubMed PMC

Press D, Akyuz M, Dural C, Aliyev S, Monteiro R, Mino J. et al. Predictors of recurrence in pheochromocytoma. Surgery 2014;156:1523–1527; discussion 7–8. PubMed

Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, et al.; Endocrine Society. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 2014;99:1915–1942. PubMed

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