The echocardiographic aspects of diagnostic of phenomenon of trabecularization of myocardium of left ventricle and non-compact myocardium
- 作者: Dzhioeva O.1,2, Kartashova E.2, Zakharova I.2, Melekhov A.1,2, Gendlin G.1,2
-
隶属关系:
- The N.I. Pirogov Russian national research medical university Minzdrav of Russia
- The municipal clinical hospital № 24 of the Moscow health department
- 期: 卷 22, 编号 1 (2016)
- 页面: 31-36
- 栏目: Articles
- URL: https://journals.rcsi.science/0869-2106/article/view/38328
- DOI: https://doi.org/10.18821/0869-2106-2016-22-1-31-36
- ID: 38328
如何引用文章
全文:
详细
作者简介
Ol’ga Dzhioeva
The N.I. Pirogov Russian national research medical university Minzdrav of Russia; The municipal clinical hospital № 24 of the Moscow health department
Email: dzhioevaon@gmail.com
MD, PhD 117997, Moscow, Russia
E. Kartashova
The municipal clinical hospital № 24 of the Moscow health department127015, Moscow, Russia
I. Zakharova
The municipal clinical hospital № 24 of the Moscow health department127015, Moscow, Russia
A. Melekhov
The N.I. Pirogov Russian national research medical university Minzdrav of Russia; The municipal clinical hospital № 24 of the Moscow health departmentКафедра госпитальной терапии № 2 лечебного факультета 117997, Moscow, Russia
G. Gendlin
The N.I. Pirogov Russian national research medical university Minzdrav of Russia; The municipal clinical hospital № 24 of the Moscow health departmentКафедра госпитальной терапии № 2 лечебного факультета 117997, Moscow, Russia
参考
- Беленков Ю.Н., Агеев Ф.Т., Мареев В.Ю. Парадоксы сердечной недостаточности: взгляд на проблему на рубеже веков. Журнал сердечная недостаточность. 2000; 1(1): 4-6.
- Сторожаков Г.И., Гендлин Г.Е., Юрпольская Л.А., Александрова С.А., Тронина О.А., Мелехов А.В. Изолированный губчатый миокард-наследственная неклассифицируемая кардиомиопатия. Журнал сердечная недостаточность. 2004;5(4): 159-62.
- Благова О.В., Недоступ А.В., Седов В.П., Гагарина Н.В., Коган Е.А., Сулимов В.А. и др. Некомпактный миокард как первичный феномен или следствие дисфункции миокарда: клинические маски синдрома. Кардиология. 2012; 52(11): 17-26.
- Chin T.K., Perloff J.K., Williams R.G., Jue K., Mohrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation. 1990; 82(2): 507-13.
- Ritter M., Oechslin E., Sutsch G., Attenhofer C., Schneider J., Jenni R. Isolated noncompaction of the myocardium in adults. Mayo Clin. Proc. 1997; 72(1): 26-31.
- Bellet S., Goulet B.A. Congenital heart disease with multiple cardiac anomalies: report of a case showing aortic atresia, fibrous scar in myocardium, and embryonal sinusoidal remains. Am. J. Med. Sci. 1932; 183: 458-65.
- Dusek J., Ostádal B., Duskova M. Postnatal persistence of spongy myocardium with embryonic blood supply. Arch. Pathol. 1975; 99: 312-7.
- Engberding R., Bender F. Identification of a rare congenital anomaly of the myocardium by two-dimensional echocardiography: persistence of isolated myocardial sinusoids. Am. J. Cardiol. 1984; 53: 1733-4.
- Chin T.K., Perloff J.K., Williams R.G., Jue K., Mohrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation. 1990; 82(2): 507-13.
- Elliott P., Andersson B., Arbustini E., Bilinska Z., Cecchi F., Charron P. et al. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases. Eur. Heart J. 2008; 29(2): 270-6.
- Sato Y., Matsumoto N., Matsuo S., Yoda S., Iida K., Kunimasa T. et al. Isolated noncompaction of the ventricular myocardium in a 94-year-old patient: depiction at echocardiography and magnetic resonance imaging. Int. J. Cardiol. 2007; 119(1): e32-4.
- Stöllberger C., Blazeck G., Winkler-Dworak M., Finsterer J. Diferencias de sexo en la ausencia de compactación con y sin trastornos neuromusculares. Rev. Esp. Cardiol. 2008; 61(2): 130-6.
- Stöllberger C., Gerecke B., Finsterer J., Engberding R. Refinement of echocardiographic criteria for left ventricular noncompaction. Int. J. Cardiol. 2013; 165(3): 463-7.
- Baldi M., Sgalambro A., Nistri S., Girolami F., Baldini K., Fantini S. et al. Clinical and genetic features of left ventricular noncompaction: a continuum in cardiomyopathies. G. Ital. Cardiol. (Rome). 2010; 11(5): 377-85.
- Hoedemaekers Y.M., Caliskan K., Michels M., Frohn-Mulder I., van der Smagt J.J., Phefferkorn J.E. et al. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy. Circ. Cardiovasc. Genet. 2010; 3: 232-9.
- Jenni R., Oechslin E., Schneider J., , Attenhofer Jost C., Kaufmann P.A. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart. 2001; 86(6): 666-71.
- Stöllberger C., Finsterer J. Pitfalls in the diagnosis of left ventricular hypertrabeculation/non-compaction. Postgrad. Med. J. 2006; 82(972): 679-83.
- Lilje C., Rázek V., Joyce J.J., Rau T., Finckh B.F, Weiss F. et al. Complications of non-compaction of the left ventricular myocardium in a paediatric population: a prospective study. Eur. Heart J. 2006; 27(15): 1855-60.
- Monserrat L., Hermida-Prieto M., Fernandez X., Rodríguez I., Dumont C., Cazón L. et al. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Eur. Heart J. 2007; 28: 1953-61.
- Hermida M., Monserrat L., Castro-Beiras A., Laredo R., Soler R., Peteiro J. et al. Familial dilated cardiomyopathy and isolated left ventricular non-compaction associated with lamin A/C gene mutations. Am. J. Cardiol. 2004; 94: 50-4.
- Hoedemaekers Y.M., Caliskan K., Majoor-Krakauer D., Van de Laar I., Michels M., Witsenburg M. et al. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies. Eur. Heart J. 2007; 28: 2732-7.
- Das K.J., Ingles J., Bagnall R.D., Semsarian C. Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment. Genet. Med. 2014; 16(4): 286-93.