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A rare cause of congenital portosystemic shunt: type 2 Abernethy malformation

100%

Taydas O. , Danisan G. , Ogul H. , Kantarci M.

Folia Morphologica

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2020

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tom 79

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nr 1

EN

The Abernethy malformation is characterised by congenital extrahepatic portosystemic shunts and is divided into two groups according to the type of anastomosis. In type 1, all portal venous blood is discharged into the inferior vena cava and there is no intrahepatic portal vein. In type 2, the portal vein is partially discharged to the inferior vena cava via side-by-side anastomoses. Imaging has an important role in the diagnosis and follow-up of this malformation. Magnetic resonance imaging should be preferred to demonstrate both vessel anatomy and associated anomalies. The aim of this study was to present a 17-year-old male patient and to discuss the imaging findings of Abernethy malformation. (Folia Morphol 2020; 79, 1: 172–175)

2

Partial anomalous pulmonary venous return associated with vascular anomalies of the aorta: multidetector computed tomography findings

88%

Bayraktutan U. , Kantarci M. , Olgun H. , Kizrak Y. , Pirimoglu B.

Folia Morphologica

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2012

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tom 71

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nr 2

EN

Partial anomalous pulmonary venous return (PAPVR) is a congenital anomaly that involves drainage of one to three pulmonary veins directly into the right heart or systemic venous system, creating a partial left-to-right shunt. This drainage is associated with cardiac abnormalities such as mitral stenosis and pulmonary stenosis, patent ductus arteriosus, and atrial septal defects. We report a case of PAPVR associated with vascular anomalies of the aorta by multidetector computed tomography in an adult female patient. (Folia Morphol 2012; 71, 2: 115–117)

3

Subvalvular membrane on the left ventricular outflow tract: multidetector computerised tomography imaging

88%

Kantarci M. , Kaygin M. A. , Bayraktutan U. , Akgul C. , Erkut B.

Folia Morphologica

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2011

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tom 70

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nr 4

EN

In this report, we describe a patient with a subvalvular membrane on the left ventricular outflow tract. Discrete subvalvular membrane is a cause of left ventricular outflow tract narrowing. Multidetector computerised tomography can demonstrate the anatomical three-dimensional view of this region and guide for surgery. (Folia Morphol 2011; 70, 4: 315–317)

4

Evaluating adult cor triatriatum with total anomalous pulmonary venous connections by multidetector computed tomography angiography

75%

Kantarci M. , Yuce I. , Yalcin A. , Arslan S. , Bozkurt M. , Gundogdu F.

Folia Morphologica

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2011

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tom 70

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nr 4

EN

A 19-year-old female patient was admitted to our hospital with dyspnea, chest pain, and shortness of breath. A chest radiograph showed mild cardiomegaly. Echocardiography revealed an extra chamber in the heart. To evaluate this abnormality, ECG-gated 16-detector-row computed tomography angiography was performed. Multidetector computed tomography (MDCT), showing cor triatriatum with total anomalous pulmonary venous connections (TAPVC), clearly revealed cardiac and vascular anatomy. ECG-gated cardiac MDCT is a useful tool for detection and characterisation of cor triatriatum and related anomalies. (Folia Morphol 2011; 70, 4: 312–314)

5

The utility of multidetector computed tomography for evaluation of congenital heart disease

63%

Bayraktutan U. , Kantarci M. , Ogul H. , Kizrak Y. , Pirimoglu B. , Genc B. , Yuceler Z. , Ceviz N.

Folia Morphologica

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2013

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tom 72

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nr 3

EN

Background: Congenital heart diseases (CHD) are the leading cause of birth defect-related deaths. Multidedector computed tomography (MDCT) plays an important role for imaging CHD in addition to echocardiography and provides a comprehensive evaluation of complex heart malformations for the referring cardiologist. The aim of the study was to evaluate the utility of MDCT in the assessment of CHD. Materials and methods: A 102 patients with CHD were investigated after initial assessment by echocardiography. The information obtained by MDCT and findings of echocardiography were reviewed together by paediatric cardiologists and cardiac radiologists. Perioperative anatomic descriptions, wherever available (n = 34) formed the gold standard for the comparison. Results: The clinical consensus diagnosis defined 154 cardiovascular lesions in the patients. The results were classified in groups. We present the appearance of various congenital cardiac lesions seen in clinical practice. Conclusions: MDCT provides important information about anatomic details of CHD for the referring cardiologist. The evaluation of different anatomic structures such as heart, great vessels, lungs and abdomen is possible in one acquisition with this technique. (Folia Morphol 2013; 72, 3: 188–196)