Cadiot G, Lehy T, Mignon M
Department of Hepato-Gastroenterology, Bichat-Claude Bernard Hospital, Paris, France.
Acta Oncol. 1993;32(2):135-40. doi: 10.3109/02841869309083902.
The Zollinger-Ellison syndrome (ZES) is characterized by hyperchlorhydria due to sustained hypergastrinemia of tumoral origin. In ZES, as in all pathological and experimental conditions associated with chronic hypergastrinemia, endocrine argyrophil cells, particularly enterochromaffin-like cells, proliferate in the fundic mucosa. In patients with ZES, fundic argyrophil carcinoids only develop in those patients who also have multiple endocrine neoplasia type 1. The authors review factors which might influence fundic argyrophil cell proliferation in the ZES. Clinical characteristics of the patients with fundic argyrophil carcinoid tumors as well as pathology and the putative mechanisms of development of these tumors are described.
佐林格-埃利森综合征(ZES)的特征是由于肿瘤源性胃泌素持续升高导致胃酸过多。与所有与慢性胃泌素血症相关的病理和实验情况一样,在ZES中,内分泌嗜银细胞,特别是肠嗜铬样细胞,在胃底黏膜中增殖。在ZES患者中,胃底嗜银类癌仅在那些同时患有1型多发性内分泌肿瘤的患者中发生。作者回顾了可能影响ZES中胃底嗜银细胞增殖的因素。描述了胃底嗜银类癌肿瘤患者的临床特征以及这些肿瘤的病理学和假定的发生机制。