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Two Cases of Adenocarcinoma Arising in Barrett's Esophagus Katsunori Aoki 1 , Eizo Kaneko 2 , Isamu Kino 3 , Yasuyuki Tokura 4 1The Second Department of Surgery, Hamamatsu University School of Medicine 2The First Department of Internal Medicine, Hamamatsu University School of Medicine 3The First Department of Pathology, Hamamatsu University School of Medicine 4Department of Surgery, Urawa City Hospital Keyword: Barrett食道 , 食道腺癌 , 食道裂孔ヘルニア , ルゴール染色 , 食道dysplasia pp.453-459
Published Date 1990/4/25
DOI https://doi.org/10.11477/mf.1403110638
  • Abstract
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 Two cases of adenocarcinoma arising in Barrett's esophagus treated in our surgical department are studied both clinically and pathologically, in order to define an acquired Barrett's esophagus, and to clarify a controversial point concerning dysplasia as a precancerous lesion.

 Case 1 was a 60-year-old man complaining of breath odor, and Case 2 was a 69-year-old woman complaining of dysphagia. Clinical examinations in these two cases revealed numerous nodular lesions beyond the squamocolumnar junction and a complication of hiatal hernia. In Case 1, a blunt dissection of the esophagus without thoracotomy was performed because of his reduced pulmonary function, and in Case 2, retrosternal esophagogastrostomy was performed through the right thoracic approach.

 The gross specimens of both cases revealed multiple Ⅱa-like elevated lesions, measurig 35 × 45 mm (Figs. 3, 4) and 40 × 45 mm (Figs. 8, 9) respectively. Microscopically, in Case 1, well differentiated adenocarcinoma was found to have infiltrated only the submucosal layer (Fig. 5), and in Case 2, mucoid adenocarcinoma had invaded the proper muscle layer (Fig. 10 a-d). These two cancers were replaced by metaplastic specialized columnar epithelium. Case 1 died of pulmonary and renal failure postoperatively, and Case 2 has been asymptomatic without evidence of recurrence for the last four years and three months.


Copyright © 1990, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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