PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT

The primary diagnosis of “dilation cardiomyopathy” is syndromal, and demands clarification of nosological origins. In the article, the specifics of such diagnostics is discussed. Clinical case is provided that illustrates the ways of management, diagnostics and treatment of the essential (primary, g...

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Main Authors: O. V. Blagova, I. N. Alieva, A. V. Nedostup, V. A. Sulimov, E. A. Kogan, A. G. Shestak, D. A. Zateyshchikov, E. V. Zaklyazminskaya
Format: Article
Language:Russian
Published: «SILICEA-POLIGRAF» LLC 2017-08-01
Series:Кардиоваскулярная терапия и профилактика
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Online Access:https://cardiovascular.elpub.ru/jour/article/view/420
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author O. V. Blagova
I. N. Alieva
A. V. Nedostup
V. A. Sulimov
E. A. Kogan
A. G. Shestak
D. A. Zateyshchikov
E. V. Zaklyazminskaya
author_facet O. V. Blagova
I. N. Alieva
A. V. Nedostup
V. A. Sulimov
E. A. Kogan
A. G. Shestak
D. A. Zateyshchikov
E. V. Zaklyazminskaya
author_sort O. V. Blagova
collection DOAJ
description The primary diagnosis of “dilation cardiomyopathy” is syndromal, and demands clarification of nosological origins. In the article, the specifics of such diagnostics is discussed. Clinical case is provided that illustrates the ways of management, diagnostics and treatment of the essential (primary, genetically determined) dilation cardiomyopathy. Patient of 22 year old with no family history, at the ages 20 and 21 y.o. had cardioembolic strokes. Paroxysmal atrial fibrillation was found, raised creatine kinase levels up to 349-1045 U/L, decreased ejection fraction 17%. Heart failure rapidly progressed. In endomyocardial biopsy there was homogenisation of cardiomyocytes, subendocardial lipomatosis with borderline virus-negative myocarditis. By Senger direct sequencing, the novel variant p.E372 in gene LMNA was found, heterozygous. Implantation of CRT-D was done, and in 4 months — cardiac transplant.
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institution DOAJ
issn 1728-8800
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language Russian
publishDate 2017-08-01
publisher «SILICEA-POLIGRAF» LLC
record_format Article
series Кардиоваскулярная терапия и профилактика
spelling doaj-art-69f1fee3eefb4023a0907c9332aee83e2025-08-20T03:18:46Zrus«SILICEA-POLIGRAF» LLCКардиоваскулярная терапия и профилактика1728-88002619-01252017-08-01164768210.15829/1728-8800-2017-4-76-82471PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENTO. V. Blagova0I. N. Alieva1A. V. Nedostup2V. A. Sulimov3E. A. Kogan4A. G. Shestak5D. A. Zateyshchikov6E. V. Zaklyazminskaya7I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University)I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University)I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University)I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University)I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University)V. B. Petrovskiy Russian National Research Centre of SurgeryVascular Center SBHI “City Clinical Hospital № 51 of the Department of Healthcare of Moscow City”I.M. Sechenov First Moscow State Medical University of the Ministry of Health (The Sechenov University); V. B. Petrovskiy Russian National Research Centre of SurgeryThe primary diagnosis of “dilation cardiomyopathy” is syndromal, and demands clarification of nosological origins. In the article, the specifics of such diagnostics is discussed. Clinical case is provided that illustrates the ways of management, diagnostics and treatment of the essential (primary, genetically determined) dilation cardiomyopathy. Patient of 22 year old with no family history, at the ages 20 and 21 y.o. had cardioembolic strokes. Paroxysmal atrial fibrillation was found, raised creatine kinase levels up to 349-1045 U/L, decreased ejection fraction 17%. Heart failure rapidly progressed. In endomyocardial biopsy there was homogenisation of cardiomyocytes, subendocardial lipomatosis with borderline virus-negative myocarditis. By Senger direct sequencing, the novel variant p.E372 in gene LMNA was found, heterozygous. Implantation of CRT-D was done, and in 4 months — cardiac transplant.https://cardiovascular.elpub.ru/jour/article/view/420dilation cardiomyopathylaminopathyendomyocardial biopsymyocarditisstrokeheart transplant
spellingShingle O. V. Blagova
I. N. Alieva
A. V. Nedostup
V. A. Sulimov
E. A. Kogan
A. G. Shestak
D. A. Zateyshchikov
E. V. Zaklyazminskaya
PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
Кардиоваскулярная терапия и профилактика
dilation cardiomyopathy
laminopathy
endomyocardial biopsy
myocarditis
stroke
heart transplant
title PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
title_full PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
title_fullStr PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
title_full_unstemmed PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
title_short PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT
title_sort primary genetically determined dilation cardiomyopathy in a patient with novel mutation of lamin gene clinical and morphological management
topic dilation cardiomyopathy
laminopathy
endomyocardial biopsy
myocarditis
stroke
heart transplant
url https://cardiovascular.elpub.ru/jour/article/view/420
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