Sawano S, Shishiba Y, Shimizu T, Ozawa Y, Miyata E, Nakazawa H, Suzuki N, Akiyama H
Division of Endocrinology and Metabolism, Toranomon Hospital, Tokyo, Japan.
Endocrinol Jpn. 1990 Apr;37(2):255-60. doi: 10.1507/endocrj1954.37.255.
Two patients with the rare association of Cushing's syndrome and primary hyperparathyroidism are reported. Initially, both patients suffered from Cushing's syndrome due to adrenal cortical adenomas with typical features and laboratory findings. Five years after treatment of the Cushing's syndrome by removal of the tumor, asymptomatic mild hypercalcemia was incidentally noticed in both patients, which suggested the occurrence of primary hyperparathyroidism. An enlarged parathyroid gland was removed surgically in both cases and was histologically shown to be a parathyroid adenoma. The levels of serum calcium returned to normal after parathyroidectomy. Papillary adenocarcinoma of the thyroid in one patient and adenomatous goiter in the other were also incidentally detected at operation. These findings suggest that Cushing's syndrome resulting from an adrenal cortical adenoma may be another presentation of multiple endocrine neoplasia type I.
报告了两例库欣综合征与原发性甲状旁腺功能亢进罕见关联的病例。最初,两名患者均因肾上腺皮质腺瘤患有库欣综合征,具有典型特征和实验室检查结果。在通过切除肿瘤治疗库欣综合征五年后,两名患者均偶然发现无症状性轻度高钙血症,提示发生了原发性甲状旁腺功能亢进。两例均通过手术切除了肿大的甲状旁腺,组织学检查显示为甲状旁腺腺瘤。甲状旁腺切除术后血清钙水平恢复正常。手术中还偶然发现一例患者患有甲状腺乳头状腺癌,另一例患有腺瘤性甲状腺肿。这些发现表明,肾上腺皮质腺瘤导致的库欣综合征可能是Ⅰ型多发性内分泌肿瘤的另一种表现形式。