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一名老年糖尿病女性患特发性精氨酸加压素缺乏症并伴有偶然发现的无功能垂体微腺瘤

Idiopathic Arginine Vasopressin Deficiency With an Incidental Non-functional Pituitary Microadenoma in an Elderly Diabetic Woman.

作者信息

Krishna Mokkarala Satya Vamsi, Babu Daruvuri Vishnu Sai Prasanna, Singh Mohini, Madhavan Sudha

机构信息

Internal Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

General Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

出版信息

Cureus. 2025 Aug 13;17(8):e89995. doi: 10.7759/cureus.89995. eCollection 2025 Aug.

Abstract

We present a case of idiopathic arginine vasopressin deficiency (AVP-D) in an elderly woman with type 2 diabetes, who presented with polyuria, polydipsia, and nocturia. Laboratory findings confirmed a euglycemic state, hyperosmolar serum, and hypoosmotic urine. Magnetic resonance imaging of the pituitary revealed the absence of the posterior bright spot and an incidental small, non-functional pituitary microadenoma, without any compressive effects on the pituitary stalk. The diagnosis of AVP-D was confirmed through a water deprivation test and a positive response to desmopressin. Common secondary causes, including inflammatory, granulomatous, and structural pathologies, were excluded. The patient responded well to oral desmopressin therapy, resulting in normalization of serum sodium and urine osmolality. This case underscores the challenges in diagnosing the cause of polyuria in a diabetic patient and the challenges in determining the etiology of AVP-D.

摘要

我们报告了一例老年2型糖尿病女性特发性精氨酸加压素缺乏症(AVP-D)的病例,该患者表现为多尿、烦渴和夜尿症。实验室检查结果证实血糖正常、血清高渗和尿低渗。垂体磁共振成像显示垂体后叶亮点缺失,偶然发现一个小的无功能垂体微腺瘤,对垂体柄无任何压迫作用。通过禁水试验和对去氨加压素的阳性反应确诊为AVP-D。排除了常见的继发性病因,包括炎症性、肉芽肿性和结构性病变。患者对口服去氨加压素治疗反应良好,血清钠和尿渗透压恢复正常。该病例强调了诊断糖尿病患者多尿病因的挑战以及确定AVP-D病因的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffe3/12429731/240493cce5dd/cureus-0017-00000089995-i01.jpg

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