1.Pulmonary stenosis after arterial switch operation for complete transposition of the great arteries(TGA).
Tadashi IKEDA ; Yoshio YOKOTA ; Fumio OKAMOTO ; Akira SHIMIZU ; Shogo NAKAYAMA ; Shuichi MATSUNO ; Shigehiro OHTANI ; Katsushi ODA ; Seiichiro MAKINO
Japanese Journal of Cardiovascular Surgery 1989;19(1):7-12
Pulmonary stenosis is the most frequent problem after arterial switch operation for TGA. We experienced four cases of late severe pulmonary stenosis out of twelve patients. All four had supravalvular stenosis either at anastomotic site or at previously banded segment. One patient had associated valvular stenosis and another had bilateral branch stenosis. It is possible that valvular stenosis was due to retraction of equine pericardial patch and branch stenosis was due to overdistension. All four cases were successfully reoperated on 13∼39 months after switch operation. To prevent late pulmonary stenosis, we now alter technique of switch operation in two points. First, the great arteries are anastomosed with interrupted U-shaped sutures from outside of the vessels in whole circumference. Second, both coronary arteries are transferred with punched-out method to save tissue of Valsalva sinus, and the defects are closed with autologous pericardial patch.
2.Combination Therapy with Rituximab and Temozolomide for Recurrent and Refractory Primary Central Nervous System Lymphoma.
Mineko MURAKAMI ; Takamitsu FUJIMAKI ; Shuichiro ASANO ; Hiroshi NAKAGUCHI ; Shoko M YAMADA ; Katsumi HOYA ; Kazuto YAMAZAKI ; Yasuo ISHIDA ; Akira MATSUNO
Yonsei Medical Journal 2011;52(6):1031-1034
High-dose methotrexate-based chemotherapy has extended survival in patients with primary central nervous system lymphoma (PCNSL). However, although salvage treatment is necessary in recurrent and refractory PCNSL, this has not been standardized. We herein describe the efficacy of a combination of rituximab and temozolomide (TMZ) in two consecutive patients with recurrent and refractory PCNSL. Based on the immunohistochemical study, case 1 had a non-germinal center B-cell-like (non-GCB) subtype, was positive for bcl-2 and negative for O6-methylguanine-DNA methyltransferase (MGMT). Case 2 was GCB subtype, bcl-2-, and MGMT+. Because of the positive expression of MGMT, interferon-beta was additionally given in case 2. Complete responses and partial responses were obtained after the third and fourth cycles of combination therapy, respectively. This was maintained for 12 months, with acceptable toxicity. The combination of rituximab and TMZ was effective in tumors with different immunohistochemical profiles. This combination therapy warrants further study in a larger population.
Aged
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Antibodies, Monoclonal, Murine-Derived/*therapeutic use
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Antineoplastic Agents/*therapeutic use
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Central Nervous System Neoplasms/*drug therapy
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Dacarbazine/*analogs & derivatives/therapeutic use
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Drug Therapy, Combination/*methods
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Humans
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Lymphoma/*drug therapy
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Male
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Middle Aged
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Neoplasm Recurrence, Local/drug therapy