Nephrology Division, Department of Internal Medicine, JA Toride Medical Center, 2-1-1 Hongo, Toride, Ibaraki, 302-0022, Japan.
Department of Endocrinology and Metabolism, Fujita Health University, Toyoake, Japan.
CEN Case Rep. 2023 Aug;12(3):297-303. doi: 10.1007/s13730-022-00769-0. Epub 2022 Dec 27.
A 36-year-old female was pointed out to have liver enzyme elevation by routine health checkup. Subsequent contrast-enhanced CT scan identified gigantic uterine fibroids and retroperitoneal tumor. She was referred to the gynecologist at JA Toride Medical Center and planned to undergo a uterus enucleation and biopsy of the retroperitoneal tumor. The surgery was conducted without any troubles. After the surgery, the patient presented polyuria with urine volume 10-20 L a day and developed hypovolemic shock. Laboratory test revealed hypotonic urine and hypernatremia. Arginine vasopressin (AVP) loading test suggested shortage of endogenous vasopressin. Since the subcutaneous administration of AVP was not sufficient to control the urine volume, continuous intravenous infusion of AVP was initiated. After achieving hemodynamic stability, the treatment was switched to oral desmopressin. MRI finding indicated attenuation of high signal in posterior pituitary in T1 weighted image while neither enlargement of pituitary nor thickening of pituitary stalk was indicated by enhanced MRI. Hypertonic salt solution test indicated no responsive elevation of AVP, confirming the diagnosis of central diabetes insipidus (CDI). Her anterior pituitary function was preserved. Only anti-rabphilin-3A antibody was found positive in the serum of the patient, while other secondary causes for CDI were denied serologically and radiologically. Hence, lymphocytic infundibuloneurohypophysitis (LINH) was suspected as the final diagnosis. Hormonal replacement therapy by nasal desmopressin was continued and the patient managed to control her urine volume. In cases of CDI considered idiopathic with conventional examinations, anti-rabphilin-3A antibody may be a clue for determining the cause as LINH.
一位 36 岁女性在常规体检时被发现肝酶升高。随后的增强 CT 扫描发现巨大的子宫肌瘤和腹膜后肿瘤。她被转介到 JA Toride 医疗中心的妇科医生处,并计划进行子宫切除术和腹膜后肿瘤活检。手术进行得很顺利。手术后,患者出现多尿,每天尿量 10-20 升,并出现低血容量性休克。实验室检查显示低张尿和高钠血症。精氨酸加压素(AVP)负荷试验提示内源性血管加压素不足。由于皮下给予 AVP 不足以控制尿量,开始持续静脉输注 AVP。在达到血流动力学稳定后,改为口服去氨加压素。MRI 结果显示 T1 加权图像中垂体后叶高信号衰减,而增强 MRI 未显示垂体增大或垂体柄增厚。高渗盐水试验表明 AVP 无反应性升高,确诊为中枢性尿崩症(CDI)。她的前垂体功能得以保留。患者血清中仅发现抗 rabphilin-3A 抗体阳性,而其他 CDI 的继发性原因在血清学和影像学上均被排除。因此,疑诊为淋巴细胞性漏斗神经垂体炎(LINH)。继续给予鼻用去氨加压素进行激素替代治疗,患者成功控制了尿量。对于常规检查考虑为特发性 CDI 的病例,抗 rabphilin-3A 抗体可能是确定 LINH 病因的线索。