基本情報
- 所属
- 自治医科大学 外科学講座(小児外科部門) 教授
- 学位
- Stat3はMn-SODを介して肝細胞における低酸素再酸素化傷害を抑制する(2005年3月 千葉大学)
- J-GLOBAL ID
- 201601010421619629
- researchmap会員ID
- B000250759
- 外部リンク
研究キーワード
11研究分野
1経歴
2-
2023年10月 - 現在
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2015年
学歴
1-
1992年4月 - 1998年3月
論文
209-
Pediatric surgery international 40(1) 240-240 2024年8月22日PURPOSE: This study aimed to clarify surgical complications associated with open surgery for congenital diaphragmatic hernia (CDH). METHODS: We performed an exploratory data analysis of the clinical characteristics of surgical complications of neonates with CDH who underwent laparotomy or thoracotomy between 2006 and 2021. Data of these patients were obtained from the database of the Japanese CDH Study Group. RESULTS: Among 1,111 neonates with left or right CDH, 852 underwent open surgery (laparotomy or thoracotomy). Of these 852 neonates, 51 had the following surgical complications: organ injury (n = 48; 6% of open surgeries); circulatory failure caused by changes in the organ location (n = 2); and skin burns (n = 1). Injured organs included the spleen (n = 30; 62% of organ injuries), liver (n = 7), lungs (n = 4), intestine (n = 4), adrenal gland (n = 2), and thoracic wall (n = 2). Fourteen of the patients who experienced organ injury required a blood transfusion (2% of open surgeries). The adjusted odds ratio of splenic injury for patients with non-direct closure of the diaphragm was 2.2 (95% confidence interval, 1.1-4.9). CONCLUSION: Of the patients who underwent open surgery for CDH, 2% experienced organ injury that required a blood transfusion. Non-direct closure of the diaphragmatic defect was a risk factor for splenic injury.
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Journal of pediatric surgery 59(8) 1451-1457 2024年8月BACKGROUND: We aimed to investigate the clinical characteristics and outcomes of patients with isolated left-sided congenital diaphragmatic hernia (CDH) who developed preoperative pneumothorax and determine its risk factors. METHODS: We performed an international cohort study of patients with CDH enrolled in the Congenital Diaphragmatic Hernia Study Group registry between January 2015 and December 2020. The main outcomes assessed included survival to hospital discharge and preoperative pneumothorax development. The cumulative incidence of pneumothorax was estimated by the Gray test. The Fine and Gray competing risk regression model was used to identify the risk factors for pneumothorax. RESULTS: Data for 2858 neonates with isolated left-sided CDH were extracted; 224 (7.8%) developed preoperative pneumothorax. Among patients with a large diaphragmatic defect, those with pneumothorax had a significantly lower rate of survival to discharge than did those without. The competing risks model demonstrated that a patent ductus arteriosus with a right-to-left shunt flow after birth (hazard ratio [HR]: 1.78; 95% confidence interval [CI]: 1.21-2.63; p = 0.003) and large defects (HR: 1.65; 95% CI: 1.13-2.42; p = 0.01) were associated with an increased risk of preoperative pneumothorax. Significant differences were observed in the cumulative incidence of pneumothorax depending on defect size and shunt direction (p < 0.001). CONCLUSIONS: Pneumothorax is a significant preoperative complication associated with increased mortality in neonates with CDH, particularly in cases with large defects. Large diaphragmatic defects and persistent pulmonary hypertension were found to be risk factors for preoperative pneumothorax development. LEVEL OF EVIDENCE: LEVEL Ⅲ Retrospective Comparative Study.
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Surgery today 2024年7月31日PURPOSE: This pilot study evaluated indocyanine green-guided near-infrared fluorescence (ICG-NIRF) imaging of testicular blood flow to predict long-term testicular atrophy after testicular torsion (TT) surgery. METHODS: The subjects of this retrospective study were patients who underwent surgery for TT at our hospital between December, 2020 and July, 2022. After detorsion, testicular blood flow was evaluated by ICG-NIRF imaging and classified into three categories: fluorescence detected, no fluorescence detected, and fluorescence detected only in the tunica albuginea vessels. Testicular volume was measured by ultrasonography up to 12 months after surgery to evaluate long-term outcomes. RESULTS: Twelve patients were included in this analysis. We found a 100% correlation between the absence of ICG-NIRF signals and subsequent testicular atrophy. In three patients without an ICG-NIRF signal, the median testis size 12 months postoperatively was significantly smaller (16.5% of the contralateral testis; range 13-20%) than that in six patients with an ICG-NIRF signal (96%; 89-115%) (p = 0.013). Mild atrophy (74.5%; 73-76%) was also observed in the three patients for whom an ICG-NIRF signal was detected only in the tunica albuginea vessels. CONCLUSIONS: Our pilot study highlights the potential of ICG-NIRF imaging as a prognostic tool for guiding surgical decision-making for patients with TT, by predicting postoperative testicular atrophy.
MISC
705-
日本小児泌尿器科学会雑誌 24(2) 216 2015年6月10日
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日本周産期・新生児医学会雑誌 51(2) 698-698 2015年6月
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日小外会誌 51(7) 1147-1152 2015年症例は9 歳男児.乳児期より長期にわたり便汚染・失禁を認めており,画像検査では直腸を中心とする部分的な腸管拡張と同部位に巨大な便腫瘤をみとめた.摘便を施行後,直腸粘膜生検を施行し,Hirschsprung 病などの器質疾患は否定された.慢性便秘の最重症例として,以後の排便管理が重要と考えたが,父子家庭であること,患児が肛門操作にトラウマがあることなどより,保存治療の長期継続が困難な状況であった.このため家族の希望もあり,拡張腸管切除術を施行した.手術所見ではS 状結腸から直腸Rs 部にかけて著明な拡張を認め,30 cm の腸管切除を施行した.吻合は機械吻合で行った.術後の排便状態は良好で,社会生活における著明なQOL の改善が得られた.術後は内服薬などの保存治療を継続していたが,術後3 年6 か月で治療を終了した.小児重症慢性便秘症において,手術適応や術式には十分な検討が必要であるが,外科治療が有用となる症例があると思われた.
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日本小児外科学会雑誌 51(7) 1190-1197 2015年胸膜肺芽腫は,胸腔内の間葉組織に由来し主に5 歳以下の小児に発症する稀な悪性腫瘍である.今回我々は,胸膜肺芽腫の治療後に腺腫様甲状腺腫を発症した1 例を経験したので報告する.症例は2 歳女児.左胸部痛,発熱を主訴に近医を受診し,胸部X 線,胸部CT にて左胸腔全体を占拠する巨大な充実性腫瘤を認め当科紹介となった.開胸腫瘍生検にて胸膜肺芽腫(type II)と診断した.遠隔転移は認めなかった.化学療法にて腫瘍の縮小をはかり,根治的腫瘍摘出術後,末梢血幹細胞移植を併用した大量化学療法を行い寛解に至った.治療終了から3 年4 か月後,甲状腺の両葉に多結節性の腫瘤を認め,甲状腺亜全摘術を施行した.術後残存甲状腺に再度多結節性腫瘤を認め,増大傾向であったため前手術から2 年後に甲状腺全摘術を施行した.病理診断はいずれも腺腫様甲状腺腫であった.初療から7 年を経過し胸膜肺芽腫,腺腫様甲状腺腫ともに再発を認めていない.
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日本小児血液・がん学会雑誌 51(4) 244-244 2014年10月
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12-
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