INTESTINE Vol.19 No.6(13-2)

Series
Title A case of carcinoma in sessile serrated adenoma / polyp with multiple endoscopic findings
Publish Date 2015/11
Author Eiji Harada Department of Gastroenterology, Akita Red Cross Hospital / Shinseikai Harada Clinic
Author Hiro-o Yamano Department of Gastroenterology, Akita Red Cross Hospital
Author Hiro-o Matsushita Department of Gastroenterology, Akita Red Cross Hospital
Author Kenjiro Yoshikawa Department of Gastroenterology, Akita Red Cross Hospital
Author Ryo Takagi Department of Gastroenterology, Akita Red Cross Hospital
Author Hironori Aoki Department of Gastroenterology, Akita Red Cross Hospital
Author Yoshihito Tanaka Department of Gastroenterology, Akita Red Cross Hospital
Author Michiko Nakaoka Department of Gastroenterology, Akita Red Cross Hospital
Author Ryogo Himori Department of Gastroenterology, Akita Red Cross Hospital
Author Makoto Nagatsuka Department of Gastroenterology, Akita Red Cross Hospital
Author Yuko Yoshida Department of Gastroenterology, Akita Red Cross Hospital
Author Tamotsu Sugai Department of Molecular Diagnostic Pathology, Iwate Medical University
Author Noriyuki Uesugi Department of Molecular Diagnostic Pathology, Iwate Medical University
Author Eiichiro Yamamoto DDepartment of Gastroenterology, Rheumatology and Clinical Immunology of Internal Medicine / Department of Molecular Biology, Sapporo Medical University
Author Hiromu Suzuki Department of Molecular Biology, Sapporo Medical University
[ Summary ] We report on a case of carcinoma in a sessile serrated adenoma/polyp (SSA/P) in an elderly woman of approximately 70 years of age. The patient presented with a Type IIa+IIc lesion (20 mm in diameter that exhibited regions of high and low elevation, with a depression in the top of the highly elevated region in the cecum (the first section of the colon).
Magnifying endoscopy indicated a Type II-open pit attern in regions of low elevation, Type Ⅱ-open/Type IIIL pit patterns in regions of high elevation, a Type VN pit pattern in the depression, and a Type VI pit pattern surrounding the depression, in which a small, tight structure could also be visualized, from a different angle. From these findings and background (e.g., location and structure), we diagnosed the lesion as a suspected Stage T1b carcinoma in SSA/P, with an additional, medullary carcinoma sited within the depression. In view of the patient's background, endoscopic mucosal resection was performed, and a histological diagnosis of carcinoma in SSA/P, cancer:well to poorly differentiated adenocarcinoma [solid type (Por1) medullary carcinoma], T1b (2,500μm), ly0, v0 was confirmed. Genetic screening of the lesion identified a BRAF mutation and CIMP in each region of the carcinoma and SSA/P. Methylation of hMLH1 was evident in the SSA/P and well-differentiated carcinoma regions, but was absent from poor to moderately differentiated carcinoma regions. We conclude that this lesion is microsatellite instability-positive colon carcinoma originating from the SSA/P. Additionally, we also conclude that the medullary carcinoma located within the depression must have arisen from a different source.
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