Frontiers in Endocrinology (Sep 2019)

Adipsic Diabetes Insipidus—The Challenging Combination of Polyuria and Adipsia: A Case Report and Review of Literature

  • Rinkoo Dalan,
  • Rinkoo Dalan,
  • Rinkoo Dalan,
  • Hanxin Chin,
  • Jeremy Hoe,
  • Abel Chen,
  • Huiling Tan,
  • Bernhard Otto Boehm,
  • Bernhard Otto Boehm,
  • Karen SuiGeok Chua

DOI
https://doi.org/10.3389/fendo.2019.00630
Journal volume & issue
Vol. 10

Abstract

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Adipsic Diabetes Insipidus is a rare hypothalamic disorder characterized by a loss of thirst in response to hypernatraemia accompanied by diabetes insipidus. These occur secondary to a congregation of defects in the homeostatic mechanisms of water balance. A 27-year old Chinese female presented with Adipsic Diabetes Insipidus after cerebral arteriovenous malformation (AVM) surgery. Initial diagnosis and management was extremely challenging. Long term management required a careful interplay between low dose vasopressin analog treatment and fluids. Detailed charts of medication and sodium balance are described in the case presentation. We performed a literature search of similarly reported cases and describe the possible pathogenesis, etiology, clinical presentation, acute and chronic management, and prognosis.

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