Isolated cardiac sarcoidosis: a case report

Introduction. Ventricular arrhythmias are a risk factor for sudden cardiac death. Abnormalities of cardiac rhythm and conduction may be the only subjective manifestation of isolated cardiac sarcoidosis, which occurs in 25% of the total number of patients with this disease.Brief description. We prese...

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Main Authors: I. A. Skomkina, V. F. Mordovin, S. V. Triss, I. V. Stepanov, N. I. Ryumshina, M. A. Polyakova, R. E. Batalov, A. Yu. Falkovskaya
Format: Article
Language:Russian
Published: «FIRMA «SILICEA» LLC 2024-06-01
Series:Российский кардиологический журнал
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Online Access:https://russjcardiol.elpub.ru/jour/article/view/5897
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author I. A. Skomkina
V. F. Mordovin
S. V. Triss
I. V. Stepanov
N. I. Ryumshina
M. A. Polyakova
R. E. Batalov
A. Yu. Falkovskaya
author_facet I. A. Skomkina
V. F. Mordovin
S. V. Triss
I. V. Stepanov
N. I. Ryumshina
M. A. Polyakova
R. E. Batalov
A. Yu. Falkovskaya
author_sort I. A. Skomkina
collection DOAJ
description Introduction. Ventricular arrhythmias are a risk factor for sudden cardiac death. Abnormalities of cardiac rhythm and conduction may be the only subjective manifestation of isolated cardiac sarcoidosis, which occurs in 25% of the total number of patients with this disease.Brief description. We present a case of isolated cardiac sarcoidosis in a young female patient, the main clinical manifestation of which was attacks of palpitations caused by ventricular tachycardia and episodes of cardiogenic shock without a cardiovascular history. Echocardiography and contrast-enhanced cardiac magnetic resonance imaging (MRI) revealed asymmetric left ventricular hypertrophy and focal myocardial masses. Cardiac tumor and sarcoidosis were suspected. The final diagnosis was based on the results of histological and immunohistochemical analysis of endomyocardial biopsies documenting sarcoidosis. No systemic manifestations of sarcoidosis were found.Discussion. The case demonstrates the potential of a comprehensive paraclinical study in the diagnosis of cardiac sarcoidosis and its differential diagnosis with other cardiac pathologies.Conclusion. Cardiac sarcoidosis is difficult to diagnose and requires histological verification in patients with LV hypertrophy and arrhythmias, and physicians should be aware about this rare disease with unfavorable prognosis without specific treatment.
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institution Kabale University
issn 1560-4071
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language Russian
publishDate 2024-06-01
publisher «FIRMA «SILICEA» LLC
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series Российский кардиологический журнал
spelling doaj-art-6a7fa04da7cd4cbb990cad59a9a747352025-08-20T03:43:46Zrus«FIRMA «SILICEA» LLCРоссийский кардиологический журнал1560-40712618-76202024-06-01292S10.15829/1560-4071-2024-58974123Isolated cardiac sarcoidosis: a case reportI. A. Skomkina0V. F. Mordovin1S. V. Triss2I. V. Stepanov3N. I. Ryumshina4M. A. Polyakova5R. E. Batalov6A. Yu. Falkovskaya7Cardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterCardiology Research Institute, Tomsk National Research Medical CenterIntroduction. Ventricular arrhythmias are a risk factor for sudden cardiac death. Abnormalities of cardiac rhythm and conduction may be the only subjective manifestation of isolated cardiac sarcoidosis, which occurs in 25% of the total number of patients with this disease.Brief description. We present a case of isolated cardiac sarcoidosis in a young female patient, the main clinical manifestation of which was attacks of palpitations caused by ventricular tachycardia and episodes of cardiogenic shock without a cardiovascular history. Echocardiography and contrast-enhanced cardiac magnetic resonance imaging (MRI) revealed asymmetric left ventricular hypertrophy and focal myocardial masses. Cardiac tumor and sarcoidosis were suspected. The final diagnosis was based on the results of histological and immunohistochemical analysis of endomyocardial biopsies documenting sarcoidosis. No systemic manifestations of sarcoidosis were found.Discussion. The case demonstrates the potential of a comprehensive paraclinical study in the diagnosis of cardiac sarcoidosis and its differential diagnosis with other cardiac pathologies.Conclusion. Cardiac sarcoidosis is difficult to diagnose and requires histological verification in patients with LV hypertrophy and arrhythmias, and physicians should be aware about this rare disease with unfavorable prognosis without specific treatment.https://russjcardiol.elpub.ru/jour/article/view/5897cardiac sarcoidosiscase reportcontrast-enhanced mriendomyocardial biopsy
spellingShingle I. A. Skomkina
V. F. Mordovin
S. V. Triss
I. V. Stepanov
N. I. Ryumshina
M. A. Polyakova
R. E. Batalov
A. Yu. Falkovskaya
Isolated cardiac sarcoidosis: a case report
Российский кардиологический журнал
cardiac sarcoidosis
case report
contrast-enhanced mri
endomyocardial biopsy
title Isolated cardiac sarcoidosis: a case report
title_full Isolated cardiac sarcoidosis: a case report
title_fullStr Isolated cardiac sarcoidosis: a case report
title_full_unstemmed Isolated cardiac sarcoidosis: a case report
title_short Isolated cardiac sarcoidosis: a case report
title_sort isolated cardiac sarcoidosis a case report
topic cardiac sarcoidosis
case report
contrast-enhanced mri
endomyocardial biopsy
url https://russjcardiol.elpub.ru/jour/article/view/5897
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AT vfmordovin isolatedcardiacsarcoidosisacasereport
AT svtriss isolatedcardiacsarcoidosisacasereport
AT ivstepanov isolatedcardiacsarcoidosisacasereport
AT niryumshina isolatedcardiacsarcoidosisacasereport
AT mapolyakova isolatedcardiacsarcoidosisacasereport
AT rebatalov isolatedcardiacsarcoidosisacasereport
AT ayufalkovskaya isolatedcardiacsarcoidosisacasereport