Mayuko Hirata
Hiroshima University
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Featured researches published by Mayuko Hirata.
Gastrointestinal Endoscopy | 2009
Hiroyuki Kanao; Shinji Tanaka; Shiro Oka; Mayuko Hirata; Shigeto Yoshida; Kazuaki Chayama
BACKGROUND There are several reports concerning the differential diagnosis of non-neoplastic and neoplastic colorectal lesions by narrow-band imaging (NBI). However, there are only a few NBI articles that assessed invasion depth. OBJECTIVE To determine the clinical usefulness of NBI magnification for evaluating microvessel architecture in relation to pit appearances and in the qualitative diagnosis of colorectal tumors. DESIGN A retrospective study. SETTING Department of Endoscopy, Hiroshima University, Hiroshima, Japan. PATIENTS AND MAIN OUTCOME MEASUREMENTS A total of 289 colorectal lesions were analyzed: 12 hyperplasias (HP), 165 tubular adenomas (TA), 65 carcinomas with intramucosal to scanty submucosal invasion (M-SM-s), and 47 carcinomas with massive submucosal invasion (SM-m). Lesions were observed by NBI magnifying endoscopy and were classified according to microvessel features and pit appearances: type A, type B, and type C. Type C was divided into 3 subtypes (C1, C2, and C3), according to the detailed NBI magnifying findings of pit visibility, vessel diameter, irregularity, and distribution. These were compared with histologic findings. RESULTS Histologic findings of HP and TA were seen in 80.0% and 20.0%, respectively, of type A lesions. TA and M-SM-s were found in 79.7% and 20.3%, respectively, of type B lesions. TA, M-SM-s, and SM-m were found in 21.6%, 29.9%, and 48.5, respectively, of type C lesions. HPs were observed significantly more often than TAs in type A lesions, TAs were observed significantly more often than carcinomas in type B lesions, carcinomas were observed significantly more often than TAs in type C (P < .01). TA, M-SM-s, and SM-m were found in 46.7%, 42.2%, and 11.1% of type C1 lesions, respectively. M-SM-s and SM-m were found in 45.5% and 54.5%, respectively, of type C2 lesions. SM-m was found in 100% of type C3 lesions. TAs and M-SM-s were observed significantly more often than SM-m in type C1 lesions, and SM-m were observed significantly more often than TAs and M-SM-s in type C3 lesions (P < .01). CONCLUSIONS NBI magnification findings of colorectal lesions were associated with histologic grade and invasion depth.
Digestive Endoscopy | 2006
Shinji Tanaka; Shiro Oka; Mayuko Hirata; Shigeto Yoshida; Iwao Kaneko; Kazuaki Chayama
Narrow band imaging (NBI) is a newly developed technology that uses optical filters for RGB sequential illumination and narrows the bandwidth of spectral transmittance. NBI enables the observation of the fine capillaries in the superficial mucosa of the gastrointestinal tract. In this report, the authors assessed the clinical usefulness of NBI magnification in pit pattern diagnosis for colorectal neoplasia. A total of 90 colorectal lesions including nine cases of hyperplasia, 60 of tubular adenoma and 21 of early carcinoma were analyzed. Histologic diagnosis was undertaken according to World Health Organization classifications. Magnified observation of the lesions was performed using NBI without chromoendoscopy, and pit pattern diagnosis was then recorded. After endoscopic or surgical resection of the lesion, the authors performed stereoscopic examination to confirm the pit pattern. From these data, the authors estimated the ability to diagnose pit patterns using NBI magnification without chromoendoscopy. The correspondence rate of pit pattern diagnosis between NBI magnification without chromoendoscopy and stereoscopic findings was 100% (9/9) for type II, 100% (56/56) for type IIIl, 100% (3/3) for type IV, 80% (12/15) for type Vi, and 57% (4/7) for type Vn. NBI magnification without chromoendoscopy demonstrated good results for pit pattern diagnosis of colorectal neoplasia, especially for lesions with regular pit pattern.
Gastrointestinal Endoscopy | 2006
Shiro Oka; Shinji Tanaka; Iwao Kaneko; Ritsuo Mouri; Mayuko Hirata; Toru Kawamura; Masaharu Yoshihara; Kazuaki Chayama
Gastrointestinal Endoscopy | 2007
Shinji Tanaka; Shiro Oka; Iwao Kaneko; Mayuko Hirata; Ritsuo Mouri; Hiroyuki Kanao; Shigeto Yoshida; Kazuaki Chayama
Gastrointestinal Endoscopy | 2007
Mayuko Hirata; Shinji Tanaka; Shiro Oka; Iwao Kaneko; Shigeto Yoshida; Masaharu Yoshihara; Kazuaki Chayama
Gastrointestinal Endoscopy | 2007
Mayuko Hirata; Shinji Tanaka; Shiro Oka; Iwao Kaneko; Shigeto Yoshida; Masaharu Yoshihara; Kazuaki Chayama
Endoscopy | 2006
S. Oka; S. Tanaka; Iwao Kaneko; Ritsuo Mouri; Mayuko Hirata; Hiroyuki Kanao; Toru Kawamura; S. Yoshida; Masaharu Yoshihara; Kazuaki Chayama
Gastrointestinal Endoscopy | 2007
Shigeto Yoshida; Shinji Tanaka; Mayuko Hirata; Ritsuo Mouri; Iwao Kaneko; Shiro Oka; Masaharu Yoshihara; Kazuaki Chayama
Acta Gastro-Enterologica Belgica | 2008
Shinji Tanaka; Mayuko Hirata; Shiro Oka; Hiroyuki Kanao; Iwao Kaneko; Sayaka Oba; Kazuaki Chayama
Acta Gastro-Enterologica Belgica | 2012
Tomoki Kobayashi; Toshio Kuwai; Haruki Kimura; Sohei Yamamoto; Keiichi Masaki; Mayuko Hirata; Atsushi Yamaguchi; Hirotaka Kono; Kazuya Kuraoka; Kiyomi Taniyama; Hiroshi Kohno