Morgello S, Schwartz E, Horwith M, King M E, Gorden P, Alonso D R
Department of Pathology, New York Hospital-Cornell Medical Center, NY 10021.
Cancer. 1988 Feb 15;61(4):800-5. doi: 10.1002/1097-0142(19880215)61:4<800::aid-cncr2820610426>3.0.co;2-3.
An insulin-containing ovarian carcinoid was found at the autopsy of a 63-year-old woman with a 12-year history of episodic hyperinsulinemic hypoglycemia. In terms of histology, the carcinoid displayed both insular and trabecular patterns and contained a small focus of mucinous cystadenoma. Beta secretory granules were demonstrated by electron microscopy, and immunoreactivity for insulin was demonstrated in tumor cell cytoplasm by immunohistochemistry. Additional autopsy findings included a solitary parathyroid adenoma and a microscopic focus of pituitary hyperplasia. This is the first recorded case of insulin production by a primary ovarian neoplasm. The patient's constellation of endocrine findings may represent a variant of the syndrome of type I multiple endocrine neoplasia.
在对一名63岁女性进行尸检时发现了一例含胰岛素的卵巢类癌,该女性有12年发作性高胰岛素血症性低血糖病史。从组织学角度来看,类癌呈现岛状和小梁状结构,并含有一小灶黏液性囊腺瘤。电镜显示有β分泌颗粒,免疫组化显示肿瘤细胞胞质内有胰岛素免疫反应性。尸检的其他发现包括一个孤立性甲状旁腺腺瘤和一个垂体增生的微小病灶。这是原发性卵巢肿瘤产生胰岛素的首例记录病例。患者的一系列内分泌表现可能代表了I型多发性内分泌肿瘤综合征的一种变异型。