Idiopathic dilatation of the right atrium. REPORT OF FOUR FETAL CASES

نویسنده

  • C. Walter
چکیده

Idiopathic dilatation of the right atrium (IDRA) is a rare anomaly defined as an isolated enlargement of the right atrium (RA) in the absence of other cardiac lesions or a condition cause RA dilatation. The clinical presentation ranging from asymptomatic to cardiac failure or even sudden death. It can be associated with atrial arrhythmias, thrombus formation and congestive heart failure. Antiplatelet prophylaxis is carried out in most described cases due to the risk of pulmonary thrombosis (and systemic if SIAD is present). The main indications for surgical reduction are rapid progression of growth, compression of adjacent structures and refractory arrhythmias. We report 4 cases of IDRA observed during prenatal diagnosis and describe the intrauterine and the postnatal course and management.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Congenital idiopathic dilatation of the right atrium: antenatal appearance, postnatal management, long-term follow-up and possible pathomechanism.

INTRODUCTION Idiopathic dilatation of the right atrium (IDRA) is a rare abnormality usually detected by chance at any time between antenatal and adult life. It is defined as isolated enlargement of the right atrium in the absence of other cardiac lesions causing right atrial dilatation. IDRA can be associated with atrial arrhythmia and systemic embolism. The clinical presentation shows high var...

متن کامل

Idiopathic dilatation of the right atrium. A case report.

Idiopathic dilatation of the right atrium in a young woman is reported. Thoracotomy was performed for suspected pericardial cyst. Intraoperative findings suggested idiopathic right atrial dilatation, which was histologically confirmed. Two years after partial resection of the dilated right atrial wall the patient is doing well. Management of asymptomatic idiopathic dilatation of the right atriu...

متن کامل

The echocardiographic diagnosis of totally anomalous pulmonary venous connection in the fetus.

BACKGROUND Infants with isolated totally anomalous pulmonary venous return often present severely decompensated, such that they are at high risk for surgical repair. On the other hand, if surgical repair can be safely accomplished, the outlook is usually good. Thus prenatal diagnosis would be expected to improve the prognosis for the affected child. OBJECTIVE To describe the features of isola...

متن کامل

REPORT OF FOUR CASES OF FAMILIAL IDIOPATHIC PULMONARY FIBROSIS

A 25 year old male and his 46 year old aunt presented with shortness of breath and a dramatic response to steroids. The other two patients are sisters with more advanced disease. One of these responded partially to steroids, while the other died within 4 months of treatment. The genetic basis and pathogenesis are discussed.

متن کامل

Multifactorial Neonatal Thrombosis in Inferior Vena Cava Dislodged to the Right Atrium: A Case Report

Background: Neonatal thrombotic diseases can cause mortality or serious morbidity and disability.Case report: In this report, we present a case of neonatal inferior vena cava thromboembolism with several underlyingfactors. Hereditary thrombophilia and genetic mutation in plasminogen activator inhibitor-1 and MTHFR A1298C genesin conjunction with cleft palate resulted in poor l...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2014