1.A Case of Patent Ductus Arteriosus with Infectious Endocarditis in Adult
Takamitsu Terasaki ; Tamaki Takano ; Toshihito Gomibuchi ; Megumi Fuke ; Kazunori Komatsu ; Kohei Takahashi ; Yuko Wada ; Tatsuichiro Seto ; Daisuke Fukui ; Jun Amano
Japanese Journal of Cardiovascular Surgery 2010;39(5):281-284
Infectious endocarditis (IE) concomitant with patent ductus arteriosus (PDA) is now considered rare because the early treatment of PDA in infancy has become standard. We report a case of PDA with IE diagnosed by computed tomography (CT). A 51-year-old man complained of arthralgia and numbness of the left extremities. He had fever of 39°C and left hemiplegia, and was referred to our hospital. A chest X-ray film showed infiltration in both lungs. CT revealed a mass lesion in the main pulmonary artery and a tubular connection between the main pulmonary artery and the aortic arch. Multiple small infarctions were also found in the brain, lungs, kidneys and spleen. Ultrasonic cardiography revealed a bi-leaflet aortic valve, and vegetations on the aortic and mitral valves. Staphylococcus aureus was detected by culture of an intravenous catheter tip. These findings suggested IE concomitant with PDA, and we started intravenous administration of antibiotics. However, congestive heart failure occurred due to severe aortic and mitral regurgitation 2 days after hospital admission, and therefore, we performed emergency surgery. The main pulmonary artery was incised after cardiopulmonary bypass was initiated. A 20-mm length of vegetation was found on the orifice of the PDA. The vegetation was removed and the PDA directly closed. Aortic and mitral valve replacement was then performed. The post-operative course was uneventful and his neurological symptoms did not exacerbate. No sign of IE recurrence was observed 2 years after the surgery. CT clearly showed PDA and vegetation in the main pulmonary artery, although ultrasonic cardiography did not. CT was useful to make a diagnosis of PDA with IE in the present case.
2.Surgical Management of Chronic Contained Rupture of an Abdominal Aortic Aneurysm Presenting as Right Lower Extremity Pain
Noburo OHASHI ; Daisuke KOMATSU ; Shuji CHINO ; Toru MIKOSHIBA ; Haruki TANAKA ; Hajime ICHIMURA ; Toshihito GOMIBUCHI ; Megumi FUKE ; Yuko WADA ; Tatsuichiro SETO
Japanese Journal of Cardiovascular Surgery 2024;53(6):354-357
Chronic contained rupture of an abdominal aortic aneurysm (AAA) is a rare condition that can present with atypical symptoms, making diagnosis challenging. We report a case of chronic contained rupture of an AAA with vertebral destruction presenting as right lower extremity pain. A 78-year-old man with a history of mitral valve replacement and pyogenic spondylitis (L2-L3) presented with a two-month history of low back pain and a four-day history of right lower extremity pain and numbness. Computed tomography revealed a 61 mm diameter ruptured AAA with an irregular margin. Magnetic resonance imaging demonstrated vertebral destruction at L4-L5. The patient underwent open surgical repair with a rifampicin-soaked graft and debridement. Intraoperatively, a large defect was found at the posterior aspect of the aneurysm, exposing the destroyed vertebral bodies. Postoperatively, the patient required spinal immobilization for persistent neurological symptoms, which improved and the patient was discharged on postoperative day 55.