Mizokami T, Inokuchi K, Okamura K, Yoshimura R, Hasuo K, Sato K, Kuroda T, Fujishima M
Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka.
Intern Med. 1996 Feb;35(2):135-41. doi: 10.2169/internalmedicine.35.135.
A 16-year-old male complained of a headache and a high fever followed by polyuria. The endocrinological studies showed he had hypopituitarism and central diabetes insipidus, and magnetic resonance imaging (MRI) revealed a pituitary mass. Diabetes insipidus gradually improved and hydrocortisone treatment was begun at three months after onset, but a month later painless thyroiditis developed. An MRI demonstrated a spontaneous shrinkage of the pituitary mass nine months after onset. Lymphocytic hypophysitis followed by painless thyroiditis was the most probable diagnosis, although it is very uncommon especially among men.
一名16岁男性主诉头痛、高热,随后出现多尿。内分泌学检查显示他患有垂体功能减退和中枢性尿崩症,磁共振成像(MRI)显示垂体有肿块。尿崩症逐渐改善,发病三个月后开始氢化可的松治疗,但一个月后出现无痛性甲状腺炎。MRI显示发病九个月后垂体肿块自发缩小。淋巴细胞性垂体炎继之以无痛性甲状腺炎是最可能的诊断,尽管这种情况非常罕见,尤其是在男性中。