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Kardiologiia

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Left fouratrial heart. First clinical case

https://doi.org/10.18087/cardio.2020.9.n619

Abstract

The left three-atrial heart (LTH) is a rare congenital abnormality where the left auricle (LA) is divided into two chambers with an additional membrane. This article describes for the first time a clinical case of congenital heart defect with four atrial chambers. A 41-old man was hospitalized for newly diagnosed paroxysmal atrial fibrillation. On transthoracic echocardiogram (EchoCG), LA was considerably enlarged and divided into two equal interconnected parts with a membrane. Additional examination with contrast-enhanced EchoCG and computed tomography revealed two membranes dividing the LA into three chambers. Prediction for the patient was beneficial since there were no other developmental abnormalities of the heart, and the LA transmembrane pressure gradient (PG) was small. Data of literature on the incidence and prognosis of LTH are provided.

About the Authors

O. S. Chumakova
Central state medical academy of department of presidential affairs, Moscow, Russia The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
Professor assistant of the department of therapy, cardiology and functional diagnostics with nephrological course


E. E. Mirzoev
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
Cardiologist of cardiological department


S. P. Pimonov
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
Radiologist


K. V. Ushakova
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
Doctor of functional diagnostics


N. M. Voloshina
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
The head of cardiological department


T. S. Arkhipkina
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
The head of functional diagnostics department


T. N. Baklanova
The Municipal clinical hospital #17, Moscow, Russia
Russian Federation
The deputy of the chief medical officer


References

1. Fuchs MM, Connolly HM, Said SM, Egbe AC. Outcomes in patients with cor triatriatum sinister. Congenital Heart Disease. 2018;13(4):628–32. DOI: 10.1111/chd.12624

2. Niwayama G. Cor triatriatum. American Heart Journal. 1960;59:291– 317. DOI: 10.1016/0002-8703(60)90287-8

3. Nassar PN, Hamdan RH. Cor Triatriatum Sinistrum: Classification and Imaging Modalities. The European Journal of Cardiovascular Medicine. 2011;1(3):84–7. DOI: 10.5083/ejcm.20424884.21

4. Rozema TK, Arruda J, Snyder CS. Cor Triatriatum: A Tale of Two Membranes. CASE. 2019;3(1):25–7. DOI: 10.1016/j.case.2018.08.003


Review

For citations:


Chumakova O.S., Mirzoev E.E., Pimonov S.P., Ushakova K.V., Voloshina N.M., Arkhipkina T.S., Baklanova T.N. Left fouratrial heart. First clinical case. Kardiologiia. 2020;60(9):149-152. (In Russ.) https://doi.org/10.18087/cardio.2020.9.n619

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ISSN 0022-9040 (Print)
ISSN 2412-5660 (Online)