1.Sternotomy Approach in a Case of Giant Ascending Aortic Aneurysm and Annuloaortic Ectasia Previously Operated for Pure Pulmonary Stenosis.
Hiroyuki Tsukui ; Shigeyuki Aomi ; Toshio Kurihara ; Goro Ohtsuka ; Masaya Kitamura ; Hitoshi Koyanagi ; Akimasa Hashimoto
Japanese Journal of Cardiovascular Surgery 1998;27(1):67-70
A 29-year-old man, who had undergone valvotomy for pure pulmonary stenosis at 6 months of age, was admitted to our institution for surgical treatment of a giant ascending aortic aneurysm and annuloaortic ectasia. Chest MRI revealed a 14-cm ascending aneurysm in contact with the sternum. After establishing femoro-femoral bypass for hypothermia, a left lateral thoracotomy was perfomed at the 4th intercostal space. Pulmonary artery cannulation was performed for left heart venting, and the proximal aortic arch was dissected for aortic cross-clamping. Median sternotomy was performed under circulatory arrest at 18°C and the aortic arch was opened. Under retrograde cerebral perfusion, the proximal arch was replaced by an artificial graft, and then aortic root replacement was completed using a composite graft under CPB. The postoperative course was uneventful, and the patient was discharged on the 37th postoperative day. He has been well without any complications. This case suggests that our method of approach to the giant aortic aneurysm with sternal adhesion and aortic regurgitation, and the use of extracorporeal circulation in view of the annuloaortic ectasia is effective and safe in case of reoperation.
2.Clinical Application of Marrow Mesenchymal Stem Cells for Hard Tissue Repair.
Hajime OHGUSHI ; Shigeyuki KITAMURA ; Noriko KOTOBUKI ; Motohiro HIROSE ; Hiroko MACHIDA ; Kaori MURAKI ; Yoshinori TAKAKURA
Yonsei Medical Journal 2004;45(Suppl):S61-S67
Human marrow mesenchymal stem cells were cultured in a medium containing glycerophosphate, ascorbic acid, and dexamethasone (Dex) on alumina ceramic discs and on tissue culture polystyrene (TCPS) dishes. Cell proliferation followed by osteogenic differentiation was observed to be equal on both culture substrata. The differentiation resulted in the appearance of bone-forming osteoblasts, which fabricated mineralized matrices on these substrata. Stem cells kept at 4degrees Cfor 24 h outside a CO2 incubator maintained a viability level of more than 90%. The regenerative cultured bone outside the incubator also maintained high alkaline phosphatase activity for several hours. These results verified that cultured bone fabricated at a cell processing center can be transported to distant hospitals for use in hard tissue repair. To date, the tissue engineered cultured bone formed on alumina ceramics in this environment have already been used in clinical situations, such as total ceramic ankle replacements.
Adult
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Aged
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Aluminum Oxide
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Bone Marrow Cells/*cytology
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Cell Differentiation
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Cell Division
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Ceramics
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Humans
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Mesenchymal Stem Cells/*cytology
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Middle Aged
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*Osteogenesis
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Research Support, Non-U.S. Gov't
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*Tissue Engineering