Vnitřní lékařství 1/2024

HLAVNÍ TÉMA Katecholamínmi indukované kardiomyopatie u pacientov s feochromocytómom | 21 / Vnitř Lék. 2024;70(1):17-21 / VNITŘNÍ LÉKAŘSTVÍ www.casopisvnitrnilekarstvi.cz ných niekoľko kazuistík, ktoré dokumentujú prípady pacientov, kde sa po transplantácii srdca pre terminálne srdcové zlyhávanie zistila prítomnosť PPGL (25, 41). Na skríning PPGL by sa malo myslieť u pacientov so srdcovým zlyhávaním, najmä ak ide o mladší vek pacienta, rezistentnú artériovú hypertenziu, paroxyzmálnu hypertenziu sprevádzanú vegetatívnou symptomatológiou. Vyšetrenie metanefrínov by malo byť však optimálne realizované až po kompenzácii a odznení akútnej fázy, pre možnú falošnú pozitivitu pri akútnych stresových stavoch (15, 25). Záver CICMP predstavujú zriedkavú, avšak veľmi závažnú až potenciálne fatálnu komplikáciu PPGL. Včasná diagnostika a adekvátny manažment vedie u väčšiny pacientov k zlepšeniu až normalizácii funkcie srdca. V prípade neliečených pacientov, resp. pacientov s inoperabilnými alebo metastatickými formami PPGL, je miera mortality vysoká, presahuje 30 %. U cca 5 % pacientov môže byť srdcové zlyhávanie prvým prejavom PPGL, preto je potrebné zvažovať PPGL v diferenciálnej diagnostike príčin niektorých druhov kardiomyopatií (25). PROHLÁŠENÍ AUTORŮ: Prohlášení o původnosti: Publikace byla zpracována s využitím uvedené literatury a nebyla publikována ani zaslána k recenznímu řízení do jiného média. Střet zájmů: Žádný. Financování: Ne. Poděkování: N/A. Registrace v databázích: N/A. Projednání etickou komisí: N/A. LITERATÚRA 1. Pacak K. New biology of pheochromocytoma and paraganglioma. Endocrine Practice. 2022;28:1253-1269. 2. Farrugia FA, Charalampopoulos A. Pheochromocytoma. Endocrine Regulations 2019; 53(3):191-212. 3. Fishbein L, et al. Pheochromocytoma and Paraganglioma: Genetics, Diagnosis, and Treatment. Hematol Oncol Clin North Am. 2016; 30(1):135-50. 4. Else T, Greenberg S, Fishbein L. Hereditary Paraganglioma-Pheochromocytoma Syndromes. 2008 May 21 [Updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1548/ 5. Eisenhofer G, Lenders JWM. Biochemical diagnosis of pheochromocytoma, a rediscovered catecholamine-metabolizing tumor. Clin Chem. 2018;64(12):1780-1781. 6. Kumar A, Pappachan JM, Fernandez CJ. Catecholamine-induced cardiomyopathy: an endocrinologist‘s perspective. Rev Cardiovasc Med. 2021;22(4):1215-1228. 7. Van Vliet PD, Burchell HB, Titus JL. Focal Myocarditis Associated With Pheochromocytoma. N Engl J Med. 1966; 274(20):1102-8. 8. Ferreira VM, Marcelino M, Piechnik SK, et al. Pheochromocytoma Is Characterized by Catecholamine-Mediated Myocarditis, Focal and Diffuse Myocardial Fibrosis, and Myocardial Dysfunction. J Am Coll Cardiol. 2016; 67(20):2364-2374. 9. Wu Y, Zeng L, Zhao S, et al. 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Efficiacy of alpha-blockers on hemodynamic control during pheochromocytoma resection: a randomized controlled trial. J Clin Endocrinol Metab. 2020;105(7):2381-91. 32. Mateucci M, Kowalewski M, Fina D et al. Extracorporeal life support for pheochromocytoma-induced cardiogenic shock: a systematic review. Perfusion. 2020;35 (1_suppl):20-28. 33. Choudhary M, Chen Y, Friedman O, et al. Pheochromocytoma Crisis Presenting With ARDS Successfully Treated With ECMO-Assisted Adrenalectomy. AACE Clin Case Rep. 2021;7(5):310-314. 34. Zhang R, Gupta D, Albert SG. Pheochromocytoma as a reversible cause of cardiomyopathy: analysis and review of the literature, Int J Cardiol. 2017;249:319-23. 35. Wani A, Adil A, Gardezi SAA et al. Pheochromocytoma presenting as hypertrophic obstructive cardiomyopathy. JAMA cardiol. 2021;6(8):974-6. 36. Huddle KR, Kalliatkis B, Skoularigis J. Pheochromocytoma associated with clinical and echocardiographic features simulating hypertrophic obstructive cardiomyopathy. Ches.t 1996;109(5):1394-7. 37. Jacob JL, da Silveira LC, de Freitas CG, et al. Pheochromocytoma with echocardiographic features of obstructive cardiomyopathy a case report. Angiology. 1994;45(11):985-9. 38. Wang Y, Yu X, Huang Y. Predictive factors for catecholamine- induced cardiomyopathy in patients with pheochromocytoma and paraganglioma. Front Endocrinol. (Lausanne) 2022;13:853878. 39. Amar J, Brunel J, Cardot Bauters C, et al. Genetic biomarkers of life-threatening pheochromocytoma-induced cardiomyopathy Endocr Relat Cancer. 2022;29(5):267-272. 40. Zhou J, Xuan H, Miao Y et al. Acute cardiac complications and subclinical myocardial injuries associated with pheochromocytoma and paraganglioma. BMC Cardiovasc Disord. 2021;21:203. 41. Dalby MC, Burke M, Radley-Smith R, et al. Pheochromocytoma presenting after cardiac transplantation for dilated cardiomyopathy. J Heart Lung Transplant. 2001;20(7):773-5.

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