A case of Arrhythmogenic right ventricular cardiomyopathy without arrhythmias

Jia Wei1, Jiang Tang1, Liming Xia2, Xinshan Chen3, Dao Wen Wang1
1Department of Internal Medicine, Tongji Hospital; Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
2Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
3Department of Forensic Pathology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

Tóm tắt

Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by recurrent coma, ventricular tachycardias and the replacement of the myocardium with fatty and fibrous tissue. We described a 42-year-old female patient without clinical arrhythmias which was diagnosed as ARVC by magnetic resonance imaging (MRI), but the transvenous endomyocardial biopsy was not specific. The patient received heart transplantation due to her refractory heart failure and the pathology of explanted heart demonstrated typical replacement of fatty and fibrous tissue and piles of infiltrated lymphocytes in myocardial tissue. It is concluded that ARVC might not have any arrhythmias and inflammatory process may be involved in the mechanism of ARVC. Virtual slides The virtual slide(s) for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/6573514507145351

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Tài liệu tham khảo

Thiene G, Corrado D, Basso C: Arrhythmogenic right ventricular cardiomyopathy/dysplasia. Orphanet J Rare Dis. 2007, 2: 45-10.1186/1750-1172-2-45.

Dalal D, et al.: Arrhythmogenic right ventricular dysplasia: a United States experience. Circulation. 2005, 112 (25): 3823-3832. 10.1161/CIRCULATIONAHA.105.542266.

Gemayel C, Pelliccia A, Thompson PD: Arrhythmogenic right ventricular cardiomyopathy. J Am Coll Cardiol. 2001, 38 (7): 1773-1781. 10.1016/S0735-1097(01)01654-0.

Hulot JS, et al.: Natural history and risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2004, 110 (14): 1879-1884. 10.1161/01.CIR.0000143375.93288.82.

Thiene G, et al.: Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med. 1988, 318 (3): 129-133. 10.1056/NEJM198801213180301.

McKenna WJ, et al.: Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. Br Heart J. 1994, 71 (3): 215-218. 10.1136/hrt.71.3.215.

Azaouagh A, et al.: Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update. Clin Res Cardiol. 2011, 100 (5): 383-394. 10.1007/s00392-011-0295-2.

Murphy DT, et al.: Cardiac MRI in arrhythmogenic right ventricular cardiomyopathy. AJR Am J Roentgenol. 2010, 194 (4): W299-W306. 10.2214/AJR.09.3450.

Corrado D, Basso C, Thiene G: Arrhythmogenic right ventricular cardiomyopathy: diagnosis, prognosis, and treatment. Heart. 2000, 83 (5): 588-595. 10.1136/heart.83.5.588.

Angelini A, et al.: Endomyocardial biopsy in right ventricular cardiomyopathy. Int J Cardiol. 1993, 40 (3): 273-282. 10.1016/0167-5273(93)90011-5.

Cooper LT: Right from the heart: when should myocardial biopsy be performed for suspected arrhythmogenic right ventricular cardiomyopathy/dysplasia?. Eur Heart J. 2008, 29 (22): 2705-2707. 10.1093/eurheartj/ehn471.

Xiaojing H, Jiannong Z, Weibo X: The utility of magnetic resonance imaging in the evaluation of arrhythmogenic right ventricular cardiomyopathy. J Radiol. 2009, 90 (6): 717-723. 10.1016/S0221-0363(09)74726-2.

Chengwei L, et al.: Diagnosis of typical and early arrhythmogenic right ventricular cardiomyopathy by novel magnetic resonance imaging. Chin J Cardiol (Chin). 2002, 30: 661-665.

Liu C, et al.: The diagnostic value of magnetic resonance imaging in arrhythmogenic right ventricular cardiomyopathy. Chin J Intern Med(Chin). 2002, 41: 191-193.

Bowles NE, et al.: The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Am Coll Cardiol. 2002, 39 (5): 892-895. 10.1016/S0735-1097(02)01688-1.

Thiene G, Basso C: Arrhythmogenic right ventricular cardiomyopathy: An update. Cardiovasc Pathol. 2001, 10 (3): 109-117. 10.1016/S1054-8807(01)00067-9.

Tavora F, et al.: Distribution of biventricular disease in arrhythmogenic cardiomyopathy: an autopsy study. Hum Pathol. 2012, 43 (4): 592-596. 10.1016/j.humpath.2011.06.014.

Corrado D, et al.: Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J Am Coll Cardiol. 1997, 30 (6): 1512-1520. 10.1016/S0735-1097(97)00332-X.

Gilljam T, Bergh CH: Right ventricular cardiomyopathy: timing of heart transplantation in Uhl's anomaly and arrythmogenic right ventricular cardiomyopathy. Eur J Heart Fail. 2009, 11 (1): 106-109. 10.1093/eurjhf/hfn014.

Yoda M, et al.: Three cases of orthotopic heart transplantation for arrhythmogenic right ventricular cardiomyopathy. Ann Thorac Surg. 2005, 80 (6): 2358-2360. 10.1016/j.athoracsur.2004.07.071.