Landman Rita E, Horwith Melvin, Peterson Ralph E, Khandji Alexander G, Wardlaw Sharon L
Department of Medicine, Columbia University College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032, USA.
J Clin Endocrinol Metab. 2002 Jul;87(7):3084-9. doi: 10.1210/jcem.87.7.8667.
A 48-yr-old woman was evaluated 21 yr after receiving treatment for an ACTH-secreting metastatic pituitary carcinoma. She had been diagnosed with Cushing's disease 35 yr earlier at the age of 14 yr and had undergone bilateral adrenalectomy. Six years later she developed Nelson's syndrome, which was treated with resection of a pituitary adenoma followed by radiotherapy to the sella turcica. Eight years later she was found to have craniospinal metastases with three remote intracerebral lesions. Two of these lesions were surgically resected and stained positive for ACTH by immunofluorescence. She subsequently received whole-brain radiotherapy and is doing well 21 yr later with no lesions seen on magnetic resonance imaging and no evidence of recurrent metastatic disease. We present this case in detail along with a literature review of ACTH-secreting pituitary carcinoma.
一名48岁女性在接受促肾上腺皮质激素(ACTH)分泌性转移性垂体癌治疗21年后接受评估。她在35年前14岁时被诊断为库欣病,并接受了双侧肾上腺切除术。六年后,她患上了尼尔森综合征,接受了垂体腺瘤切除术,随后对蝶鞍进行了放射治疗。八年后,她被发现有颅脊髓转移,伴有三个远处脑内病变。其中两个病变经手术切除,免疫荧光染色显示ACTH呈阳性。她随后接受了全脑放疗,21年后情况良好,磁共振成像未发现病变,也没有复发性转移性疾病的迹象。我们详细介绍了该病例,并对ACTH分泌性垂体癌的文献进行了综述。