Nagai S, Shimizu C, Kimura Y, Umetsu M, Taniguchi S, Takeuchi J, Atsumi T, Yoshioka N, Kubo M, Koike T
Division of Endocrinology and Metabolism, Department of Medicine II, Hokkaido University Graduate School of Medicine, 060-8638 Sapporo, Japan.
J Endocrinol Invest. 2006 Apr;29(4):367-72. doi: 10.1007/BF03344111.
Hypopituitarism can be caused by tumor, inflammation, granuloma and injuries. Once pituitary function is disturbed, hormone replacement therapy is necessary for the remaining life span in most cases. We have experienced a rare case of a unique intrasellar mass associated with pituitary dysfunction in which both spontaneously reversed. A 61-yr-old woman developed hypoadrenalism and central diabetes insipidus (cDI). Magnetic resonance (MR) imaging revealed a lobular, strong hypointense lesion with spotty signal in the middle of the hypophysis. This spotty lesion showed isointensity on T1- and high-intensity on T2-weighted MR images. The spotty signal as well as the normal pituitary lobe were enhanced by the administration of gadolinium. As replacement therapies for hypoadrenalism and cDI, 10 mg of hydrocortisone and 2.5 microg of desmopressin acetate were prescribed. Three months later, slight shrinkage of intrasellar mass and spontaneous improvement of pituitary functions were found. Hydrocortisone was then discontinued. Furthermore, because polyuria and polydipsia were improved nine months later, desmopressin acetate was stopped. Currently, the intrasellar mass continues to shrink, and the patient shows no symptoms without medication. Based upon the unique features of MR images, we suspect that the origin of the mass is an intrasellar hemangioma.
垂体功能减退可由肿瘤、炎症、肉芽肿和损伤引起。一旦垂体功能受到干扰,在大多数情况下,余生都需要进行激素替代治疗。我们遇到过一例罕见病例,一个独特的鞍内肿块与垂体功能障碍相关,而两者均自发逆转。一名61岁女性出现肾上腺功能减退和中枢性尿崩症(cDI)。磁共振(MR)成像显示垂体中部有一个小叶状、明显低信号的病变,伴有斑点状信号。这个斑点状病变在T1加权MR图像上呈等信号,在T2加权MR图像上呈高信号。注射钆后,斑点状信号以及正常垂体叶均有强化。作为肾上腺功能减退和cDI的替代疗法,开具了10毫克氢化可的松和2.5微克醋酸去氨加压素。三个月后,发现鞍内肿块略有缩小,垂体功能自发改善。随后停用了氢化可的松。此外,由于九个月后多尿和多饮症状有所改善,停用了醋酸去氨加压素。目前,鞍内肿块持续缩小,患者未用药也无任何症状。基于MR图像的独特特征,我们怀疑该肿块起源于鞍内血管瘤。