Kaizaki Y, Fujii T, Kawai T, Saito K, Kurihara K, Fukayama M
Department of Pathology, Jichi Medical School, Tochigi, Japan.
J Gastroenterol. 1997 Oct;32(5):643-9. doi: 10.1007/BF02934114.
We report a case of gastric neuroendocrine (NE) carcinoma associated with chronic atrophic gastritis type A (CAG/A) or reversed atrophic type gastritis. A 9 x 6 cm tumor was resected from the stomach to control pain in a 55-year-old Japanese woman with peritoneal dissemination and metastatic tumors of the liver and ovary. Histologically, the tumor was NE carcinoma which showed an organoid structure, but consisted of NE cells with overt cytological atypia and frequent mitotic activity. Multiple microcarcinoids and NE cell micronests (NECMs) were also observed in the atrophic non-neoplastic mucosa of the gastric body. CEA immunoreactivity and a high Ki-67 labeling index were characteristic features of the neoplastic NE cells of the carcinoma. Although most NE tumors arising from CAG/A are typical carcinoid tumors, the present case illustrates that a high-grade NE carcinoma can develop from diverse NE cell proliferation in association with CAG/A.
我们报告一例与A型慢性萎缩性胃炎(CAG/A)或逆萎缩型胃炎相关的胃神经内分泌(NE)癌。从一名55岁日本女性的胃中切除了一个9×6cm的肿瘤,以控制其腹膜播散以及肝脏和卵巢转移瘤引起的疼痛。组织学上,该肿瘤为神经内分泌癌,呈器官样结构,但由具有明显细胞学异型性和频繁有丝分裂活性的神经内分泌细胞组成。在胃体萎缩性非肿瘤性黏膜中也观察到多个微类癌和神经内分泌细胞微巢(NECM)。癌组织中肿瘤性神经内分泌细胞的特征性表现为癌胚抗原免疫反应性和高Ki-67标记指数。尽管大多数源于CAG/A的神经内分泌肿瘤是典型类癌,但本例表明,高级别神经内分泌癌可由与CAG/A相关的多种神经内分泌细胞增殖发展而来。