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Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up

机译:随访4年后永久性中枢性尿崩症伴垂体柄增生完全消退

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摘要

A 14 year−old patient was admitted because of a history of polyuria and polydipsia. A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made. Hypophyseal magnetic resonance imaging (MRI) of the patient demonstrated isolated pituitary stalk enlargement. Although GH deficiency and gonadotropin deficiency were transient, CDI was persistent despite the regression of the pituitary stalk enlargement over the 4 years of follow−up.
机译:一名14岁的患者因多尿和多饮水史而入院。诊断为中枢性尿崩症(CDI)并伴有生长激素(GH)和促性腺激素缺乏症。患者的垂体磁共振成像(MRI)表现为孤立的垂体柄增大。尽管生长激素缺乏症和促性腺激素缺乏症是一过性的,但尽管在4年的随访中垂体柄增大,但CDI仍然持续存在。

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