Yang Lei-Yi, Lin Sang, Xie Qi-Bing, Yin Geng
Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Medicine (Baltimore). 2020 Oct 23;99(43):e22939. doi: 10.1097/MD.0000000000022939.
Some diseases contribute to hypopituitarism without clinical manifestations and the glucocorticoid therapy may unveil central diabetes insipidus. The condition is rare and usually causes problems for clinical physicians.
A 59-year-old woman presented to our hospital due to facial numbness and persistent eyelid heaviness.
Physical examination and cerebrospinal fluid examination supported a diagnosis of Guillain-Barre[Combining Acute Accent] syndrome. Magnetic resonance imaging showed an empty sella. Hormone test indicated hypopituitarism.
The patient received intravenous immunoglobulin and glucocorticoid. Central diabetes insipidus appeared after 20 days. Subsequently, the patient was prescribed 1-desamino-8-D-arginine vasopressin and prednisone.
During 6 months' follow-up, the patient's urine output was gradually reduced to normal level.
This case indicated that hypopituitarism may be caused by an empty sella and be masked by adrenal insufficiency. Central diabetes insipidus may present after glucocorticoid therapy.
某些疾病可导致垂体功能减退但无临床表现,糖皮质激素治疗可能会引发中枢性尿崩症。这种情况较为罕见,通常会给临床医生带来困扰。
一名59岁女性因面部麻木和持续性眼睑沉重前来我院就诊。
体格检查和脑脊液检查支持吉兰-巴雷综合征的诊断。磁共振成像显示为空蝶鞍。激素检测表明存在垂体功能减退。
患者接受了静脉注射免疫球蛋白和糖皮质激素治疗。20天后出现中枢性尿崩症。随后,为患者开具了去氨加压素和泼尼松。
在6个月的随访期间,患者尿量逐渐降至正常水平。
该病例表明垂体功能减退可能由空蝶鞍引起,并被肾上腺功能不全所掩盖。糖皮质激素治疗后可能出现中枢性尿崩症。