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Michael Weidenbach

Publications (4)

Giant Intrapericardial Teratoma – Enough Space Left in the Neonatal Thorax?

Michael Weidenbach, Christian Paech, Frauke Hornemann & Marcel Vollroth · Cardiology and Angiology: An International Journal · 2020

Objective: Optimal treatment of fetal intrapericardial teratoma is controversial, especially in regard to fetal intervention. Given the rarity of the disease case reports can assist in decision making. Case Report: We report on a neonate with a giant intrapericardial teratoma det...

Open access Research Article 10.9734/ca/2020/v9i430147

Truncus Arteriosus with Anomalous Origin and Intramural Course of the Right Coronary Arterie: A Surgical Challenge

Marcel Vollroth, Michael Weidenbach, Ingo Dähnert, Martin Kostelka & Robert Wagner · Cardiology and Angiology: An International Journal · 2020

The truncus arteriosus communis is a very complex congenital cardiac malformation occurring in less than 1% of all congenital heart disease patients. Early repair remains one of the most challenging procedures in congenital cardiac surgery. Due to improvement in surgical reconstr...

Open access Research Article 10.9734/ca/2020/v9i130123

Unguarded Tricuspid Orifice with Congenitally Corrected Transposition of the Great Arteries and Aortic Atresia- A Highly Unusual Case

Carolin Puegge, Isabell Altmann & Michael Weidenbach · Cardiology and Angiology: An International Journal · 2021

Unguarded tricuspid orifice is a very rare anomaly. It is characterised by the absence of one or more of the tricuspid valve leaflets resulting in severe tricuspid regurgitation and right heart failure. It is rarely an isolated anomaly but more often associated with pulmonary atr...

Open access Research Article 10.9734/ca/2021/v10i430181

Cavitary Pulmonary Aspergilloma after Norwood-I-Procedure - A Rare Complication after Delayed Sternal Closure in a Patient with HLHS

Robert Wagner, Marcel Vollroth, Martin Kostelka, Christian Paech, Reinhard Berner, Ingo Daehnert & Michael Weidenbach · Cardiology and Angiology: An International Journal · 2017

The presented case is the first to report on a child with hypoplastic left heart syndrome (HLHS) with invasive aspergillosis (IA) progressing to cavitary pulmonary aspergillosis after Norwood stage I procedure.  

Open access Research Article 10.9734/CA/2017/37814