Gastric remnant cancer as a metachronous multiple lesion

The pathological characteristics and natural history of 35 gastric remnant cancers after partial gastrectomy for a malignant condition and 16 gastric cancers after gastrectomy for benign conditions were compared. Gastric remnant cancer following malignant disease was characterized by a well defined...

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Published in:British journal of surgery Vol. 80; no. 1; p. 54
Main Authors: Furukawa, H, Iwanaga, T, Hiratsuka, M, Imaoka, S, Ishikawa, O, Kabuto, T, Sasaki, Y, Kameyama, M
Format: Journal Article
Language:English
Published: England 01-01-1993
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Abstract The pathological characteristics and natural history of 35 gastric remnant cancers after partial gastrectomy for a malignant condition and 16 gastric cancers after gastrectomy for benign conditions were compared. Gastric remnant cancer following malignant disease was characterized by a well defined rather than diffuse appearance (in 43 versus 12 per cent of gastric remnant cancers after benign conditions, P < 0.05), location away from the anastomosis (83 versus 25 per cent, P < 0.05) and a shorter interval after the first operation (5-14 versus > or = 20 years, P < 0.01). The 15- and 16-year survival rates appeared to be worse for gastric remnant cancer after malignant than after benign disease, but there was no statistically significant difference between the two groups in a generalized Wilcoxon test. In the former, direct invasion to adjacent organs was frequently observed. These findings suggest that gastric remnant cancer after gastrectomy for malignancy may be a metachronous multiple lesion, while that following benign disease may occur as a new cancer caused by the partial gastrectomy. To improve the survival of patients with cancer after gastrectomy for malignancy, a rational extended operation may be useful.
AbstractList The pathological characteristics and natural history of 35 gastric remnant cancers after partial gastrectomy for a malignant condition and 16 gastric cancers after gastrectomy for benign conditions were compared. Gastric remnant cancer following malignant disease was characterized by a well defined rather than diffuse appearance (in 43 versus 12 per cent of gastric remnant cancers after benign conditions, P < 0.05), location away from the anastomosis (83 versus 25 per cent, P < 0.05) and a shorter interval after the first operation (5-14 versus > or = 20 years, P < 0.01). The 15- and 16-year survival rates appeared to be worse for gastric remnant cancer after malignant than after benign disease, but there was no statistically significant difference between the two groups in a generalized Wilcoxon test. In the former, direct invasion to adjacent organs was frequently observed. These findings suggest that gastric remnant cancer after gastrectomy for malignancy may be a metachronous multiple lesion, while that following benign disease may occur as a new cancer caused by the partial gastrectomy. To improve the survival of patients with cancer after gastrectomy for malignancy, a rational extended operation may be useful.
Author Kabuto, T
Sasaki, Y
Furukawa, H
Ishikawa, O
Kameyama, M
Imaoka, S
Iwanaga, T
Hiratsuka, M
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  surname: Furukawa
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  organization: Department of Surgery, Centre for Adult Diseases, Osaka, Japan
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  surname: Iwanaga
  fullname: Iwanaga, T
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  surname: Hiratsuka
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  surname: Imaoka
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  surname: Ishikawa
  fullname: Ishikawa, O
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  surname: Kabuto
  fullname: Kabuto, T
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  givenname: Y
  surname: Sasaki
  fullname: Sasaki, Y
– sequence: 8
  givenname: M
  surname: Kameyama
  fullname: Kameyama, M
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Snippet The pathological characteristics and natural history of 35 gastric remnant cancers after partial gastrectomy for a malignant condition and 16 gastric cancers...
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StartPage 54
SubjectTerms Adult
Aged
Aged, 80 and over
Female
Gastrectomy - adverse effects
Gastrectomy - mortality
Humans
Male
Middle Aged
Risk Factors
Stomach Neoplasms - etiology
Stomach Neoplasms - mortality
Stomach Neoplasms - pathology
Time Factors
Title Gastric remnant cancer as a metachronous multiple lesion
URI https://www.ncbi.nlm.nih.gov/pubmed/8428294
Volume 80
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