2024/04/03 更新

写真a

ウエツキ コウタ
植月 康太
UETSUKI Kota
所属
医学部附属病院 消化器内科 病院助教
職名
病院助教
 

論文 7

  1. Endoscopic ultrasound-guided drainage using a forward-viewing echoendoscope for peripancreatic fluid collection after Child resection

    Ishikawa, T; Yamao, K; Mizutani, Y; Iida, T; Uetsuki, K; Nakamura, M; Kawashima, H

    ENDOSCOPY   56 巻 ( S 01 ) 頁: E83 - E84   2024年12月

     詳細を見る

    記述言語:英語   出版者・発行元:Endoscopy  

    DOI: 10.1055/a-2234-4075

    Web of Science

    Scopus

    PubMed

  2. An atypical case of isolated immunoglobulin G4-related sclerosing cholangitis with a cholangiogram resembling primary sclerosing cholangitis

    Takada, Y; Ishikawa, T; Yamao, K; Mizutani, Y; Iida, T; Uetsuki, K; Kawashima, H

    CLINICAL JOURNAL OF GASTROENTEROLOGY   17 巻 ( 2 ) 頁: 338 - 344   2024年4月

     詳細を見る

    記述言語:英語   出版者・発行元:Clinical Journal of Gastroenterology  

    An asymptomatic 77-year-old man with intrahepatic bile duct dilation was referred to our hospital. Cholangiography revealed alternations between strictures and dilated segments from the right and left hepatic ducts to the lower bile ducts, with findings of a pruned tree, beaded, shaggy appearance, and diverticulum-like outpouching. Histopathology revealed abundant immunoglobulin G4 (IgG4)-positive plasma cells (> 10 per high-power field) with an IgG4/IgG-positive cell ratio of 40–50%. After 2 weeks of steroid therapy, the cholangiography markedly improved. Because the cholangiographic findings resembled those of primary sclerosing cholangitis, steroid therapy proved useful in differentiating IgG4-related sclerosing cholangitis from primary sclerosing cholangitis.

    DOI: 10.1007/s12328-023-01903-w

    Web of Science

    Scopus

    PubMed

  3. Outcomes of endoscopic papillectomy of ampullary carcinoma and factors affecting additional surgery

    Takada, Y; Ishikawa, T; Yamao, K; Mizutani, Y; Iida, T; Uetsuki, K; Gibo, N; Ohno, E; Kawashima, H

    JOURNAL OF HEPATO-BILIARY-PANCREATIC SCIENCES   31 巻 ( 2 ) 頁: 110 - 119   2024年2月

     詳細を見る

    記述言語:英語   出版者・発行元:Journal of Hepato-Biliary-Pancreatic Sciences  

    Background/Purpose: Data on the prognosis of endoscopic papillectomy (EP) for ampullary carcinoma (AC) is limited; therefore, we aimed to identify the factors associated with endoscopically controlled AC. Methods: Between January 2003 and October 2022, 75 patients underwent EP for ampullary tumors and were diagnosed with AC based on the pathological features of the resected tissue. The factors associated with additional surgery after EP were also evaluated. Results: A total of 67 patients had ACs ranging from carcinoma in situ to tumors limited to the mucosa (M group), and eight patients had ACs ranging from those limited to the sphincter of Oddi to those invading the duodenal muscularis propria (OD group). The 3-year endoscopic tumor control (condition not requiring additional surgery) rates in the M and OD groups were 90.8% and 84.6% (p =.033), respectively. In the M group, the presence of tumor components in the resection margins was the only significant factor associated with additional surgeries (p =.010) in the univariate analysis. The 3-year endoscopic tumor control rates were 100% for negative and uncertain resection margins and 76.6% for positive margins (p =.009). Conclusions: If the AC is confined to the mucosa and the resection margins are negative or uncertain, the tumor can be well-controlled endoscopically.

    DOI: 10.1002/jhbp.1375

    Web of Science

    Scopus

    PubMed

  4. Current status of and future issues related to endoscopic papillectomy

    Kawashima, H; Ishikawa, T; Yamao, K; Mizutani, Y; Iida, T; Uetsuki, K; Yamamura, T; Furukawa, K; Nakamura, M

    NAGOYA JOURNAL OF MEDICAL SCIENCE   85 巻 ( 4 ) 頁: 648 - 658   2023年11月

     詳細を見る

    記述言語:英語   出版者・発行元:Nagoya Journal of Medical Science  

    Endoscopic papillectomy is widely performed to treat duodenal papillary tumors, particularly at highvolume centers. It is indicated for adenomas without intraductal extension of the bile or pancreatic ducts. However, despite numerous reports of carcinomas that expand the indications to include well-differentiated adenocarcinomas that do not invade the sphincter of Oddi, the low agreement between biopsy and final pathological diagnosis, as well as the current inability of imaging modalities to diagnose sphincter of Oddi invasion, makes it difficult to consider expanding indications. Although complications can be prevented by certain methods, such as pancreatic duct stenting, and the frequency of severe complications has decreased, the safety of the procedure remains unconfirmed. In the future, this technology is expected to progress and enable wider applications, including those in tumors with extensive horizontal spread and those with intraductal extension of the bile and pancreatic ducts. Such technology may also improve the safety and accuracy of diagnosis.

    DOI: 10.18999/nagjms.85.4.648

    Web of Science

    Scopus

    PubMed

  5. 1型自己免疫性膵炎に合併する胆管病変の狭窄部位からみた臨床像と長期予後

    石川 卓哉, 山雄 健太郎, 水谷 泰之, 飯田 忠, 植月 康太, 宜保 憲明, 片岡 邦夫, 森 裕, 高田 善久, 青井 広典, 南 喜之, 川嶋 啓揮

    胆道   37 巻 ( 4 ) 頁: 754 - 762   2023年10月

     詳細を見る

    記述言語:日本語   出版者・発行元:一般社団法人 日本胆道学会  

    <p>1型自己免疫性膵炎(AIP)159例について胆管病変の有無による臨床像を比較し,長期予後を検討した.89例(56%)に胆管病変を認め,胆管病変合併例ではCA19-9が有意に高く(<i>P</i><0.001),ステロイド投与率が有意に高かった(<i>P</i>=0.001).中央値42.9カ月の観察期間で再燃を49例(30.8%)に認め,膵内胆管より上流まで狭窄・壁肥厚を認めた症例で有意に累積再燃率が高く(3年:24% vs. 37.1%,<i>P</i><0.001),2回以上再燃する率も高かった(5.1% vs. 19.5%,<i>P</i>=0.01).再燃例の多くはステロイド増量により改善したが,肝内胆管まで狭窄・拡張を認めた2例でステロイド依存性となり,アザチオプリンを併用した.膵内胆管より上流まで狭窄・壁肥厚を認める1型AIPでは再燃を繰り返す率が高く,特に肝内胆管まで狭窄・拡張を認める症例ではステロイド依存性となり得る.</p>

    DOI: 10.11210/tando.37.754

    CiNii Research

  6. 症例報告 特発性細菌性腹膜炎を合併した急性膵炎後の皮下結節性脂肪壊死症の1例

    天野 友里恵, 桃原 真理子, 竹内 想, 河野 通浩, 秋山 真志, 倉田 信彦, 植月 康太

    臨床皮膚科   77 巻 ( 11 ) 頁: 921 - 925   2023年10月

     詳細を見る

    出版者・発行元:株式会社医学書院  

    DOI: 10.11477/mf.1412207126

    CiNii Research

  7. 胆嚢及び膵臓に形質細胞腫を伴った多発性骨髄腫の1例

    宜保 憲明, 野々垣 浩二, 大野 栄三郎, 青木 聡典, 八鹿 潤, 植月 康太, 飯田 忠, 水谷 泰之, 山雄 健太郎, 石川 卓哉, 宇野 雄祐, 川嶋 啓揮

    胆道   37 巻 ( 1 ) 頁: 83 - 90   2023年3月

     詳細を見る

    記述言語:日本語   出版者・発行元:一般社団法人 日本胆道学会  

    <p>症例は84歳男性.腰痛と食欲不振を契機に,高カルシウム血症,腎不全,高蛋白血症が明らかとなり,骨髄穿刺などを経て多発性骨髄腫と診断された.造影CTで,胆嚢頚部に僅かに造影される不整形腫瘤を認めた.また,同様の造影効果を示す類円形腫瘤を膵尾部,右胸腔,腹腔にそれぞれ認めた.超音波内視鏡では,胆嚢病変は高低エコーが混在した不整形腫瘤として,膵尾部病変は無エコーと低エコーが混在した類円形腫瘤としてそれぞれ描出された.両病変に対して行った超音波内視鏡下穿刺吸引法で,いずれの検体からも異型を伴う形質細胞が認められ,共に形質細胞腫と最終診断した.1次治療のMPB療法は奏効せず,胆嚢腫瘤増大に伴う閉塞性黄疸を発症した.しかし,胆管ステンティング後に開始された2次治療のLd療法では,M蛋白の減少や高カルシウム血症の改善と共に胆嚢病変と膵尾部病変の縮小も認められ,臨床経過も形質細胞腫として矛盾しなかった.</p>

    DOI: 10.11210/tando.37.83

    CiNii Research

▼全件表示