An 82-year-old woman was given emergency admission because of severe anterior chest pain. We found an ascending aortic aneurysm 60mm in diameter. CT revealed acute aortic dissection with an ascending aorta. Emergeny operation was performed under a diagnosis of type-A acute aortic dissection with ascending aortic aneurysm. Operative findings showed thrombus in the dissection and a dilated ascending aorta without intimal tears. Operative findings differed from those of a classical dissection and were compatible with a diagnosis of aortic intramural hematoma (IMH). We performed hemi-arch replacement for the ascending aortic aneurysm under deep hypothermic cardiac arrest and she was discharged without any complications. IMH in the presence of coexisting ascending aortic aneurysm is extremely rare and we therefore reported the surgical repair of this rare case.

We report a rare case of surgical treatment for acute type A aortic dissection with expansion of the false lumen. The patient was a 72-year-old man without any motor paresis who underwent total aortic arch replacement with two-vessel perfusion of SCP and mild hypothermic circulatory arrest for the lower half of the body. Postoperatively, the patient had tetraparesis which was more severe than in his lower extremities, whereas the sensory function was preserved. It was assumed that the anterior horns of the spinal cord were injured longitudinally due to insufficient blood flow of the anterior spinal artery through the SCP. This case suggests that three-vessel perfusion of SCP is important in surgical treatment for acute type A aortic dissection for the prevention of intraoperative ischemic spinal cord injury.

A 77-year-old man with an abnormal shadow on chest x-ray film, was found to have Kommerell's diverticulum associated with a right aortic arch 2 years previously. During the period of follow-up, the Kommerell's diverticulum was expanded to 5.3 cm in diameter. CT revealed a right aortic arch with mirror-image branching and Kommerell's diverticulum. To eliminate the risk of rupture, the Kommerell's diverticulum was excluded by deployment of a handmade fenestrated stent-graft using the brachial wire traction technique via the right femoral artery and left brachial artery. At 30-months of follow-up the patient is doing well, with no signs of endoleak or migration. Endovascular repair of Kommerell's diverticulum with a right aortic arch is feasible, safe and effective. This is a rare case of a right aortic arch with Kommerell's diverticulum and without left aberrant subclavian artery.

We report a case of successful graft replacement of the total aortic arch using selective cerebral perfusion for recurrent distal aortic arch aneurysm (DAAA). A 72-year-old man who had a history of patch aortoplasty for saccular DAAA was admitted to our hospital. Computed tomography and digital subtraction angiography showed recurrent saccular DAAA and coronary angiography revealed 90% stenosis of the first diagonal branch, resulting in a diagnosis of recurrent DAAA with coronary artery stenosis. A graft replacement of the total aortic arch with the aid of selective cerebral perfusion and coronary artery bypass grafting to the first diagonal branch was carried out. Postoperatively, he had no cerebral complications. One year after the operation, he had an operation for an abdominal aortic aneurysm. The patient is now leading a normal life.

A 81-year-old-man was diagnosed with the acute myocardial infarction （AMI） and ventricular septal defects （VSD）. He was medically treated under the intra-aortic balloon pumping （IABP） for 2 weeks after the onset of AMI, and underwent the surgical VSD closure by the extended sandwich technique. Surgery was performed with the right ventriculotomy. The infarction was extensive in the ventricular septum and the right ventricular posterior papillary muscle was resected during myectomy of the infarcted septum to prevent the residual shunt. VSD was closed by two patches from the left and right ventricles. Tricuspid valve was completely prolapsed due to the resected papillary muscle and tricuspid valve replacement was required. Postoperative echocardiography showed no residual shunt and normal tricuspid valve function. The patient was discharged 114 days after surgery. The present case suggests the possibility of the right ventricular papillary muscle resection and tricuspid valve treatment during VSD closure by the right ventriculotomy.