Atypical Partial Anomalous Pulmonary Venous Drainage of the Left Upper Pulmonary Vein Through a Compressed Vertical Vein Between the Aorta and the Pulmonary Artery

2011 ◽  
Vol 32 (8) ◽  
pp. 1271-1272
Author(s):  
Habiba Mizouni ◽  
Monia Attia ◽  
Jalel Zaidi ◽  
Emna Menif
2019 ◽  
Vol 3 (2) ◽  
Author(s):  
Paulo Henrique Manso ◽  
Valéria de Melo Moreira ◽  
Vera Demarchi Aiello

Abstract Background Scimitar syndrome consists of anomalous pulmonary vein drainage to the inferior vena cava. Its name derives from the image this anomalous pulmonary vein creates on a chest radiograph. We describe a case of normal venous pulmonary vein drainage that also presented the scimitar sign due to an aorto-collateral vessel. Case summary A 15-month-old girl presented with mild dyspnoea and fever. Control chest X-ray showed an image of cardiac dextroposition, hypoplastic right lung, and the ‘scimitar sign’. Although the transthoracic echocardiogram confirmed the initial suspicion of anomalous pulmonary venous drainage, the computed tomography (CT) scan showed normal right pulmonary veins connected to the left atrium and revealed that an aorto-collateral vessel caused the scimitar sign. Discussion Although the patient had several typical alterations of the scimitar syndrome, the pulmonary venous connection was normal, and the scimitar sign was due to an aorto-collateral vessel. It might be difficult to describe venous pulmonary connections on the basis of echocardiography, so an angio CT scan proved to be a valuable tool in this scenario.


2007 ◽  
Vol 96 (7) ◽  
pp. 511-513 ◽  
Author(s):  
Ingo Dähnert ◽  
Frank-Thomas Riede ◽  
Martin Kostelka

PEDIATRICS ◽  
1991 ◽  
Vol 87 (4) ◽  
pp. 584-585
Author(s):  
WILLIAM C. KIRBY

In Reply.— We certainly agree with Dr Noonan's comments regarding the association of partial anomalous venous drainage (PAPVD) and Turner's syndrome. We also have anecdotal information about several additional patients with Turner syndrome and PAPVD. Knowledge of such patients does not define further the overall incidence of these venous anomalies in the population of patients with 45,XO karyotype. Our study demonstrates that patients with only a single anomalous pulmonary vein may have quite subtle clinical findings.


2018 ◽  
Vol 28 (3) ◽  
pp. 514-515
Author(s):  
Toshiyuki Iwaya ◽  
Koichi Sughimoto ◽  
Kagami Miyaji

AbstractWe describe the case of a 21-year-old patient who underwent repairs for multiple lesions including aortic and pulmonary valve replacements, right ventricular outflow tract reconstruction, revision of the right pulmonary artery route, and a repair of partial anomalous pulmonary venous drainage, which was diagnosed during this fourth sternotomy. For these patients with adult CHD, it is most important to address all underlying factors as much as possible at the redo surgery.


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