Ishizuka H, Atobe T, Kurose T, Katou O, Tsurumi K
Gan No Rinsho. 1983 Dec;29(15):1772-8.
We report a case of primary stomach carcinoma arising in the atypical epithelium, which was accompanied with ossification. The patient was a 73-year-old man, who was operated because of the possibility of advanced Type IIa carcinoma. Grossly, a large papillary polypoid lesion was recognized in the anterior wall of the antrum near the pylorus ring. Histological study revealed well differentiated tubular adenocarcinoma arising in the atypical epithelium; ossification was found in the stroma without necrosis, calcification or chondrification. Ossification arising in primary stomach carcinoma is very rare. Only five cases of ossification in primary stomach carcinoma have been reported in the world literature; two of these were Japanese patients. Probably ours is the first reported case with both stomach carcinoma and ossification arising in the atypical epithelium.
我们报告一例起源于非典型上皮且伴有骨化的原发性胃癌。患者为一名73岁男性,因可能存在进展期IIa型癌而接受手术。大体上,在幽门环附近胃窦前壁可见一个大的乳头状息肉样病变。组织学研究显示,非典型上皮中出现高分化管状腺癌;间质中发现骨化,无坏死、钙化或软骨化生。原发性胃癌中出现骨化非常罕见。世界文献中仅报道了5例原发性胃癌骨化病例;其中2例为日本患者。我们的病例可能是首例报道的同时存在胃癌且骨化起源于非典型上皮的病例。