Abboud P, Bart H, Mansour G, Pinteaux A, Birembaut P
Department of Gynecology and Obstetrics, Hospital of Soissons, Reims, France.
Am J Obstet Gynecol. 2001 Jan;184(2):237-8. doi: 10.1067/mob.2001.108856.
We report a very rare case of ovarian gastrinoma in the context of multiple endocrine neoplasia type I, including primary hyperparathyroidism and Zollinger-Ellison syndrome. Somatostatin receptor scintigraphy revealed the ovarian involvement at an early stage. Oophorectomy led to the final diagnosis and complete healing.
我们报告了一例非常罕见的I型多发性内分泌腺瘤病患者合并卵巢胃泌素瘤的病例,该患者同时患有原发性甲状旁腺功能亢进症和卓-艾综合征。生长抑素受体闪烁扫描在早期就发现了卵巢受累情况。卵巢切除术最终确诊并实现了完全治愈。