Feasibility of a nanomaterial-tissue patch for vascular and cardiac reconstruction

2015 ◽  
Vol 104 (3) ◽  
pp. 449-457 ◽  
Author(s):  
Allison M. Ostdiek ◽  
Jan R. Ivey ◽  
Sarah A. Hansen ◽  
Raja Gopaldas ◽  
Sheila A. Grant
Keyword(s):  
Cardiac Reconstruction

Four-dimensional cardiac reconstruction from rotational x-ray sequences: first results for 4D coronary angiography

2009 ◽  
Author(s):  
Eberhard Hansis ◽  
Hermann Schomberg ◽  
Klaus Erhard ◽  
Olaf Dössel ◽  
Michael Grass
Keyword(s):  
Coronary Angiography ◽  
X Ray ◽  
First Results ◽  
Cardiac Reconstruction ◽  
Ray Sequences

scholarly journals Left Atrial Appendage Closure Guided by Personalized 3D-Printed Cardiac Reconstruction

2015 ◽  
Vol 8 (7) ◽  
pp. 1004-1006 ◽  
Author(s):  
James M. Otton ◽  
Roberto Spina ◽  
Romina Sulas ◽  
Rajesh N. Subbiah ◽  
Neil Jacobs ◽  
...  
Keyword(s):  
Left Atrial ◽  
Left Atrial Appendage ◽  
Atrial Appendage ◽  
Left Atrial Appendage Closure ◽  
3D Printed ◽  
Cardiac Reconstruction

scholarly journals Right Thoracoabdominal Approach for Retrocardiac Paraganglioma Resection

2017 ◽  
Vol 44 (1) ◽  
pp. 62-65
Author(s):  
Carlos A. Hinojosa ◽  
Hugo Laparra-Escareno ◽  
Javier E. Anaya-Ayala ◽  
Rene Lizola ◽  
Adriana Torres-Machorro ◽  
...  
Keyword(s):  
Cardiopulmonary Bypass ◽  
Arterial Hypertension ◽  
Surgical Approach ◽  
Tumor Resection ◽  
Complete Resection ◽  
Adrenal Tumors ◽  
Thoracoabdominal Approach ◽  
Cardiac Reconstruction ◽  
Thoracoabdominal Incision

Paragangliomas are rare extra-adrenal tumors of sympathetic or parasympathetic paraganglia origin; of these, mediastinal paragangliomas are 2% of all cases. We present the case of a 21-year-old woman with uncontrolled arterial hypertension who had a functioning 6.5 × 6.2-cm retrocardiac paraganglioma firmly attached to the pericardium. The patient underwent tumor resection via a right thoracoabdominal incision; this surgical approach enabled adequate exposure for complete resection without institution of cardiopulmonary bypass or need for cardiac reconstruction or autotransplantation. Ten months postoperatively, the patient was doing well and was no longer hypertensive.

scholarly journals Capillary haemangioma of the heart presenting with pericardial effusion: A case report

2020 ◽  
Vol 13 (3) ◽  
pp. 250-253
Author(s):  
Anshuman Darbari ◽  
Devender Singh ◽  
Shegu Gilbert ◽  
Barun Kumar ◽  
Neha Singh
Keyword(s):  
Pericardial Effusion ◽  
Main Pulmonary Artery ◽  
Pericardial Fluid ◽  
Histopathological Analysis ◽  
Tumour Mass ◽  
Flow Area ◽  
Capillary Haemangioma ◽  
Cardiac Tumours ◽  
Positron Emission ◽  
Cardiac Reconstruction

Cardiac haemangiomas (CH) are rare benign primary tumours of the heart and constitute nearly 2.8% of primary cardiac tumours. In a-48-year-old female, a cardiac tumour mass over right ventricular out flow area and main pulmonary artery was detected during diagnostic workup for aetiology of recurrent pericardial effusion. Echocardiograhy and pericardial fluid findings were non conclusive. Contrast enhanced Computed tomography (CECT) and Positron emission tomography (PET) scan imaging found the exophytic, moderately hypermetabolic, heterogeneous mass lesion posterolateral to main pulmonary trunk. We did partial resection of lesion without cardiac reconstruction and open incisional biopsy through midline sternotomy incision. Histopathological analysis confirmed this as a case of Capillary type of haemangioma of heart.

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