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©2009 The WJG Press and Baishideng.
World J Gastroenterol. May 14, 2009; 15(18): 2177-2183
Published online May 14, 2009. doi: 10.3748/wjg.15.2177
Published online May 14, 2009. doi: 10.3748/wjg.15.2177
Table 1 Characteristics of GC types
| Type 1 | Type 2 | Type 3 | |
| Percentage (%) | 70-85 | 5-10 | 15-25 |
| Tumor characteristics | Often small, multiple, polypoid, multicentric | Often small, multiple, polypoid, multicentric | Single, > 1-2 cm, polypoid and often ulcerated |
| Mean age at diagnosis (yr) | 63 | 50 | 55 |
| Gender | Females > males | Females = males | Males > females |
| Associated conditions | Chronic atrophic gastritis type A | ZES/MEN1 | Sporadic |
| Serum gastrin levels | Increased | Increased | Normal |
| pH of gastric juice | Increased | Low | Normal |
| Ki-67 (%) | Usually < 2 | Usually < 2 | Usually > 2 |
| Metastases (%) | 2-5 | < 10 | > 50 |
Table 2 Clinicopathological characteristics of endocrine tumors of the stomach according to WHO classification[23]
| Well-differentiated tumor-carcinoid |
| Benign behavior: confined to mucosa-submucosa, non-angioinvasive, ≤ 1 cm in size, non-functioning |
| ECL cell tumor of corpus-fundus associated with hypergastrinemia and chronic atrophic gastritits (CAG) or MEN1 syndrome |
| Serotonin-producing tumor |
| Gastrin-producing tumor |
| Uncertain behavior: confined to mucosa-submucosa, > 1 cm in size, or angioinvasive |
| ECL cell tumor with CAG or MEN1 syndrome or sporadic |
| Serotonin-producing tumor |
| Gastrin-producing tumor |
| Well-differentiated endocrine carcinoma-malignant carcinoid |
| Low-grade malignant, deeply invasive (muscularis propria or beyond), or with metastasis |
| Nonfunctioning |
| ECL cell carcinoid, usually sporadic, rarely in CAG or MEN1 syndrome |
| Serotonin-producing tumor |
| Gastrin-producing tumor |
| Functioning |
| ECL cell carcinoid with atypical carcinoid syndrome |
| Serotonin-producing carcinoid with syndrome |
| Gastrin-producing carcinoma-malignant gastrinoma |
| ACTH-producing carcinoma with Cushing syndrome |
| Poorly differentiate endocrine carcinoma-small cell carcinoma, high grade malignant, usually non-functioning, occasionally with Cushing syndrome |
Table 3 Proposed TNM staging system for GC tumors[7]
| Primary tumor | ||||
| Depth of invasion | Size | |||
| T1 | Up to and including muscularis propria | ≤ 3 cm | ||
| T2 | Beyond muscularis propria | ≤ 3 cm | ||
| T3 | Up to and including muscularis propria | > 3 cm | ||
| Beyond muscularis propria | > 3 cm | |||
| Lymph node | ||||
| N0 | No lymph node metastasis | |||
| N1 | Regional lymph node metastasis | |||
| Distant metastasis | ||||
| M0 | No distant metastasis | |||
| M1 | Distant metastasis | |||
| Disease stage | T | N | M | |
| I | T1 | Any N | M0 | |
| II | T2 | N0 | M0 | |
| T3 | N0 | M0 | ||
| III | T2 | N1 | M0 | |
| IV | T3 | N1 | M0 | |
| Any T | Any N | M1 | ||
- Citation: Massironi S, Sciola V, Spampatti MP, Peracchi M, Conte D. Gastric carcinoids: Between underestimation and overtreatment. World J Gastroenterol 2009; 15(18): 2177-2183
- URL: https://www.wjgnet.com/1007-9327/full/v15/i18/2177.htm
- DOI: https://dx.doi.org/10.3748/wjg.15.2177
