Editorial
Copyright ©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
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