Brain Pathol. 2012 Jul;22(4):575-8. doi: 10.1111/j.1750-3639.2012.00607.x.
A 52 year-old male with a history of Cushing's Disease at age 18 and bilateral adrenalectomy at age 23 presented with visual changes. An MRI scan showed a pituitary macroadenoma (Nelson's syndrome). Other than the development of diabetes mellitus at age 32, his disease was stable until presentation. Serum studies show markedly elevated ACTH levels, but he had no hyperpigmentation. The tumor was removed by endoscopic surgery. Microscopic examination showed a pituitary adenoma with strong immunostaining for ACTH. In addition, the tumor cells showed Crooke's hyaline change and stained strongly for cytokeratin (Crooke's Cell Adenoma). Normal pituitary was not present. Crooke's cell adenomas are extremely rare and have not been previously reported in Nelson's Syndrome.
一位 52 岁男性,18 岁时患有库欣病,23 岁时行双侧肾上腺切除术,现出现视力改变。MRI 扫描显示垂体大腺瘤(纳尔逊综合征)。除 32 岁时发生糖尿病外,他的病情一直稳定,直到出现症状。血清研究显示 ACTH 水平显著升高,但他没有色素沉着。肿瘤通过内镜手术切除。显微镜检查显示垂体腺瘤 ACTH 免疫染色强阳性。此外,肿瘤细胞出现 Crooke 透明变,细胞角蛋白染色强阳性(Crooke 细胞腺瘤)。未见正常垂体。Crooke 细胞腺瘤非常罕见,以前在纳尔逊综合征中没有报道过。