INTESTINE Vol.22 No.1(13)


連載名 第25回大腸IIc研究会優秀演題
題名 病理・遺伝子背景において興味深い所見を呈した上行結腸癌の1例
発刊年月 2018年 01月
著者 田中 義人 秋田赤十字病院消化器病センター/岩手医科大学医学部病理診断学講座
著者 山野 泰穂 秋田赤十字病院消化器病センター/札幌医科大学医学部消化器内科学講座
著者 松下 弘雄 秋田赤十字病院消化器病センター
著者 永塚 真 岩手医科大学医学部病理診断学講座
著者 菅井 有 岩手医科大学医学部病理診断学講座
著者 山本 英一郎 札幌医科大学医学部消化器内科学講座/札幌医科大学医学部分子生物学講座
著者 鈴木 拓 札幌医科大学医学部分子生物学講座
【 要旨 】 70歳代,男性.便潜血反応陽性の精査として全大腸内視鏡検査を施行したところ,上行結腸に径約20 mmのLSTを指摘された.大部分が白色調であったが,一部に発赤調の部分を認め,色素拡大観察では白色調の部分ではII型および伸II型pitを,発赤調の部分ではVI型pitおよびIVB型pitを認めた.以上より過形成性ポリープを由来とし腺腫を経て癌へ進展した病変あるいは衝突病変を疑った.病理組織診断では現在の鋸歯状病変のカテゴリーのいずれにも当てはまらない管状腺管の増殖に管状腺腫と高分化管状腺癌の混在,さらに中分化管状腺癌を認め,深達度はpT1a (SM 300 µm),脈管侵襲は陰性であった.遺伝子解析では一元的な癌化病変である可能性が示唆されたが,serrated pathwayやadenoma-carcinoma sequenceを支持する所見は認めなかった.
Series
Title Case of ascending colon cancer : pathologically and genetically interesting findings
Author Yoshihito Tanaka Department of Gastroenterology, Akita Red Cross Hospital / Department of Molecular Diagnostic Pathology, Iwate Medical University
Author Hiro-o Yamano Department of Gastroenterology, Akita Red Cross Hospital / Department of Gastroenterology and Hepatology, Sapporo Medical University
Author Hiro-o Matsushita Department of Gastroenterology, Akita Red Cross Hospital
Author Makoto Eizuka Department of Molecular Diagnostic Pathology, Iwate Medical University
Author Tamotsu Sugai Department of Molecular Diagnostic Pathology, Iwate Medical University
Author Eiichiro Yamamoto Department of Gastroenterology and Hepatology, Sapporo Medical University / Department of Molecular Biology, Sapporo Medical University
Author Hiromu Suzuki Department of Molecular Biology, Sapporo Medical University
[ Summary ] A man in his 70s underwent a total colonoscopy following a positive fecal occult blood test. A laterally spreading tumor (LST) with a dimeter of 20 mm was found in the ascending colon. The major part of the tumor was white, but some section were reddish. Magnifying chromoendoscopy revealed that the white part was Type II and Type II-long pit and that the reddish parts were Type VI and Type IVB pit. Based on these results, we suspected that the adenomas derived from hyperplastic polyps developed into cancer or that this was a collision tumor. In pathological examination, we observed a proliferation of tubular ducts which did not fall into any current categories of serrated lesions. We also observed the mixture of tubular adenoma and well differentiated tubular adenocarcinoma. In addition, we observed a moderately differentiated tubular adenocarcinoma. Tumor depth of invasion was pT1a (SM 300 µm) and no vascular invasion was observed. The results of genetic analysis suggest that this is a genetically homogenous tumor. However, no findings support that this tumor developed through a serrated pathway and adenoma-carcinoma sequences were obtained.
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