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Title of Journal: Pituitary

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Abbravation: Pituitary

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Springer US

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DOI

10.1016/0026-0657(95)91358-0

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1573-7403

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Adipsic diabetes insipidus in adult patients

Authors: Martín Cuesta Mark J Hannon Christopher J Thompson
Publish Date: 2017/01/10
Volume: 20, Issue: 3, Pages: 372-380
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Abstract

Adipsic diabetes insipidus ADI is a very rare disorder characterized by hypotonic polyuria due to arginine vasopressin AVP deficiency and failure to generate the sensation of thirst in response to hypernatraemia As the sensation of thirst is the key homeostatic mechanism that prevents hypernatraemic dehydration in patients with untreated diabetes insipidus DI adipsia leads to failure to respond to aquaresis with appropriate fluid intake This predisposes to the development of significant hypernatraemia which is the typical biochemical manifestation of adipsic DIADI has been reported to occur in association with clipping of an anterior communicating artery aneurysm following subarachnoid haemorrhage major hypothalamic surgery traumatic brain injury and toluene exposure among other conditions Management is very difficult and patients are prone to marked changes in plasma sodium concentration in particular to the development of severe hypernatraemia Associated hypothalamic disorders such as severe obesity sleep apnoea and thermoregulatory disorders are often observed in patients with ADIThe management of ADI is challenging and is associated with significant morbidity and mortality Prognosis is variable hypothalamic complications lead to early death in some patients but recent reports highlight the possibility of recovery of thirstThis article does not contain any studies with human participants or animals performed by any of the authors All procedures performed in prior studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards


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  2. Erratum to: An endoscopic modification of the simultaneous ‘above and below’ approach to large pituitary adenomas
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  8. Pituitary tumor apoplexy in patients with Cushing’s disease: endocrinologic and visual outcomes after transsphenoidal surgery
  9. A comparison of cabergoline and bromocriptine on the risk of valvular heart disease in patients with prolactinomas
  10. Sellar and clival plasmacytomas: case series of 5 patients with systematic review of 65 published cases
  11. Analysis of GNAS mutations in 60 growth hormone secreting pituitary tumors: correlation with clinical and pathological characteristics and surgical outcome based on highly sensitive GH and IGF-I criteria for remission
  12. Sellar plasmacytomas: a concise review
  13. Increased clinical symptoms of acromegalic arthropathy in patients with long-term disease control: a prospective follow-up study
  14. Two cases of Kallmann syndrome associated with empty sella
  15. Multiple head and neck tumors following treatment for craniopharyngioma
  16. Modulation of VEGF/Flk-1 receptor expression in the rat pituitary GH3 cell line by growth factors
  17. Acromegalic gigantism, physicians and body snatching. Past or present?
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  19. Pituitary gland and β-catenin signaling: from ontogeny to oncogenesis
  20. Differential diagnosis of ACTH-dependent hypercortisolism: imaging versus laboratory
  21. A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred

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