以尿崩症为表现的韦格纳肉芽肿病。
Wegener's granulomatosis presenting as diabetes insipidus.
作者信息
Dutta P, Hayatbhat M, Bhansali A, Bambery P, Kakar N
机构信息
Department of Endocrinology, Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
出版信息
Exp Clin Endocrinol Diabetes. 2006 Oct;114(9):533-6. doi: 10.1055/s-2006-924122.
PMID:17115352
Abstract
Pituitary gland involvement in Wegener's granulomatosis (WG) occurs most commonly in the form of central diabetes insipidus (CDI). However, CDI as a presenting manifestation of WG is very rare. We report two such cases; one of them had multi-organ involvement at presentation, while other developed it during follow-up. CDI was reversible following cytotoxic drug therapy in one of them.
摘要
垂体受累于韦格纳肉芽肿病（WG）最常见的形式是中枢性尿崩症（CDI）。然而，CDI作为WG的首发表现非常罕见。我们报告两例这样的病例；其中一例在初诊时有多器官受累，而另一例在随访期间出现。其中一例经细胞毒性药物治疗后CDI可逆。
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