基本情報
- 所属
- 自治医科大学 総合医学第一講座 教授
- 学位
- 医学博士
- ORCID ID
https://orcid.org/0000-0002-5036-9282
- J-GLOBAL ID
- 201801010081278303
- researchmap会員ID
- B000334131
研究キーワード
3研究分野
5論文
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Annals of vascular diseases 17(3) 287-291 2024年9月25日A 53-year-old woman visited her district hospital complaining of right lower limb numbness 8 days after being diagnosed with COVID-19. She had been suffering diarrhea for 25 days before the hospital visit. Computed tomography showed multiple arterial and venous thromboses, and anticoagulation with a therapeutic dose of heparin was initiated. Acute aortic occlusion occurred on hospital day 5, and balloon thromboembolectomy was performed for revascularization of the lower limbs 9 hours after onset. Ulcerative colitis was diagnosed on postoperative day 7. With the anticoagulation and immunosuppression therapy, no thromboembolic event occurred postoperatively.
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BMC nephrology 25(1) 53-53 2024年2月9日BACKGROUND: Minimal change nephrotic syndrome (MCNS) can be complicated by thymoma; however, no standard therapy for thymoma-associated MCNS has yet been established. We herein describe a case of steroid-resistant MCNS associated with thymoma, treated effectively with rituximab. CASE PRESENTATION: A 71-year-old Japanese man was referred to our department with severe proteinuria (20 g/gCr). Renal biopsy showed minimal change disease and computed tomography revealed an anterior mediastinal mass. Based on these findings, he was diagnosed with thymoma-associated MCNS. He was treated with oral prednisolone (50 mg/day) and cyclosporine, and underwent thymectomy and plasma exchange. However, no improvement in proteinuria was observed. He therefore received intravenous rituximab 500 mg, resulting in a marked decrease in proteinuria from 5328 to 336 mg/day after 1 week. CONCLUSIONS: This case suggests that rituximab might be an effective therapy in patients with steroid-resistant MCNS associated with thymoma.
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Cancer diagnosis & prognosis 4(6) 715-721 2024年BACKGROUND/AIM: In prostate cancer, robotic total prostatectomy is a popular treatment modality. However, prostate-specific antigen (PSA) recurrence after prostate cancer surgery remains a concern. Salvage radiotherapy is commonly used to treat PSA recurrence, but the recurrence rate after salvage radiotherapy is high, highlighting the need for better predictive markers. This study aimed to retrospectively evaluate the association between cribriform pattern and PSA recurrence in patients receiving radiotherapy after radical prostatectomy. PATIENTS AND METHODS: Data of 50 patients who underwent radiotherapy after total prostatectomy between January 2010 and May 2020 were retrospectively evaluated. The median age was 67 years. Among these patients, two cases involved postoperative irradiation, while 48 cases involved salvage irradiation after postoperative PSA recurrence. The median time from surgery to PSA recurrence was 38.3 months. The median radiation dose was 64 Gy in 32 fractions. Three-dimensional conformal radiation therapy was administered in 38 cases and intensity-modulated radiation therapy was used in 12 cases. Combined hormone therapy was administered in 21 cases. PSA levels were measured every 3 months after treatment. Statistical analysis between groups was performed by a t-test. RESULTS: The median follow-up period after radiotherapy was 31 months. No local recurrences were observed at the prostate bed, and no deaths related to prostate cancer were recorded during follow-up. However, 18 patients (36.0%) had PSA recurrence. The PSA recurrence rate based on the cribriform pattern was 17.6% in the none to moderate group (34 patients) and 75.0% in the severe cribriform pattern group (16 patients). The PSA recurrence rate was significantly higher in patients with a severe invasive cribriform pattern (p=0.001). No significant differences were observed in other histopathological characteristics. CONCLUSION: The cribriform pattern in surgical pathology specimens was found to be a useful predictor of PSA recurrence after postoperative radiotherapy.
MISC
97-
日本病理学会会誌 108(1) 303-303 2019年4月
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JOURNAL OF UROLOGY 193(4) E537-E537 2015年4月
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JOURNAL OF THORACIC ONCOLOGY 8 S753-S754 2013年11月
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JOURNAL OF THORACIC ONCOLOGY 6(6) S1053-S1054 2011年6月
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日本臨床外科学会雑誌 = The journal of the Japan Surgical Association 72(2) 379-383 2011年2月25日症例は6歳,男児.Henoch-Schönlein紫斑病(HSP)に対し,前医にてステロイドや第XIII因子,ウリナスタチンの投与,ステロイドパルス療法などの対処療法を行ったが,紫斑,腹痛,下血は徐々に増悪した.腎機能障害も出現し,第16病日当院小児科紹介入院となった.再度ステロイドパルス療法,ステロイド投与を行い,症状・検査データーともに一時改善に向かったが,第24病日腹痛再燃,翌日腹部筋性防御が出現,消化管穿孔の診断で同日緊急手術を施行した.回腸に約50cmにわたる壊死腸管を認め,穿孔が多発しており,同部を切除し吻合した.病理組織学検査にて,HSPに特有な血栓や血管炎の所見は乏しく,またHE染色で巨細胞封入体,免疫組織化学染色でCMV陽性像を認めた.血液検査にてCMVアンチゲネミア陽性,以上よりCMV腸炎の合併が証明され,穿孔の原因であると考えられた.早期のステロイド減量を心掛け,術後33日目退院となった.
共同研究・競争的資金等の研究課題
10-
日本学術振興会 科学研究費助成事業 基盤研究(C) 2020年4月 - 2024年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2017年4月 - 2020年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2017年4月 - 2020年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2016年4月 - 2020年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2015年4月 - 2017年3月