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特发性精氨酸血管加压素缺乏症伴轻度可逆性高钙血症

Idiopathic Arginine Vasopressin Deficiency With Mild and Reversible Hypercalcemia.

作者信息

Malik Aayush, Goyal Alpesh, Gupta Rahul, Bhagat Abhinav

机构信息

Department of Endocrinology and Metabolism, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.

Department of Radiodiagnosis, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.

出版信息

Ochsner J. 2025 Spring;25(1):67-72. doi: 10.31486/toj.24.0089.

Abstract

BACKGROUND

Arginine vasopressin deficiency (central diabetes insipidus) results from impaired hypothalamic-neurohypophyseal secretion of arginine vasopressin and leads to hypotonic polyuria and polydipsia. Common causes of arginine vasopressin deficiency include head trauma, pituitary surgery, neoplasms, and inflammatory stalk lesions; however, 25% to 50% of cases are idiopathic. Hypercalcemia can result in arginine vasopressin resistance (nephrogenic diabetes insipidus) and is an important differential in the evaluation of patients with hypotonic polyuria-polydipsia syndrome.

CASE REPORT

A 32-year-old male presented with polyuria (24-hour urine output of 144 mL/kg), polydipsia (24-hour fluid intake of 130 mL/kg), and nocturia of 6 months' duration. Baseline investigations revealed normal liver, renal, serum potassium, and blood glucose levels. After overnight dehydration, serum osmolality increased to 317 mOsm/kg, while urine osmolality remained inappropriately low at 156 mOsm/kg. Mild hypercalcemia (serum calcium of 11.1 mg/dL) was noted. Upon arginine vasopressin challenge, urine osmolality increased by nearly 300%, suggesting complete arginine vasopressin deficiency. Evaluation for secondary causes was unremarkable. Magnetic resonance imaging of the pituitary revealed a normal anterior pituitary and pituitary stalk with an absent posterior pituitary bright spot. Idiopathic arginine vasopressin deficiency was diagnosed. The patient responded to oral desmopressin replacement, and normocalcemia was documented in multiple samples repeated when the patient was in a hydrated state.

CONCLUSION

Patients with arginine vasopressin deficiency can manifest concomitant mild and reversible dehydration-related hypercalcemia. A brisk increase in urine osmolality following subcutaneous arginine vasopressin injection and normal serum calcium levels after desmopressin therapy can establish that hypercalcemia is the effect and not the cause of the primary disorder.

摘要

背景

精氨酸加压素缺乏(中枢性尿崩症)是由下丘脑 - 神经垂体分泌精氨酸加压素受损所致,会导致低渗性多尿和烦渴。精氨酸加压素缺乏的常见原因包括头部外伤、垂体手术、肿瘤和炎性垂体柄病变;然而,25%至50%的病例为特发性。高钙血症可导致精氨酸加压素抵抗(肾性尿崩症),是评估低渗性多尿 - 烦渴综合征患者时的重要鉴别点。

病例报告

一名32岁男性出现多尿(24小时尿量为144 mL/kg)、烦渴(24小时液体摄入量为130 mL/kg)及夜尿,病程6个月。基线检查显示肝、肾、血清钾和血糖水平正常。过夜脱水后,血清渗透压升至317 mOsm/kg,而尿渗透压仍不适当地低,为156 mOsm/kg。发现轻度高钙血症(血清钙为11.1 mg/dL)。给予精氨酸加压素激发试验后,尿渗透压增加近300%,提示完全性精氨酸加压素缺乏。对继发性病因的评估无异常。垂体磁共振成像显示垂体前叶和垂体柄正常,垂体后叶亮点缺失。诊断为特发性精氨酸加压素缺乏。患者对口服去氨加压素替代治疗有反应,在患者处于水合状态时多次重复检测显示血钙正常。

结论

精氨酸加压素缺乏患者可表现出伴随的轻度且可逆的脱水相关高钙血症。皮下注射精氨酸加压素后尿渗透压迅速升高以及去氨加压素治疗后血清钙水平正常,可确定高钙血症是原发性疾病的结果而非原因。

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