Literature DB >> 20119738

SIADH following pituitary adenoma apoplexy.

Florian Heinrich Ebner1, Till K Hauser, Juergen Honegger.   

Abstract

The rare case of a patient with SIADH following pituitary adenoma apoplexy is reported. Since apoplexy did not exert any mass effect on surrounding structures, the patient was treated conservatively and the anterior pituitary gland insufficiency has been substituted adequately. Seven days after the apoplexy the patient again showed low serum-Na(+) levels despite cortisol substitution. Diagnosis of SIADH was made. It is essential to be aware of this rare syndrome in patients with pituitary adenoma apoplexy.

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Year:  2010        PMID: 20119738     DOI: 10.1007/s10072-009-0210-z

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  2 in total

1.  [An interesting case of pituitary apoplexy showing abnormality in water-electrolyte before and after surgery].

Authors:  K Morinaga; Y Inoue; M Ueda; Y Matsumoto; N Omiya; J Mikami; H Satou; S Okawara
Journal:  No To Shinkei       Date:  1990-10

2.  Pituitary apoplexy and inappropriate ADH secretion.

Authors:  Deepak Agrawal; A K Mahapatra
Journal:  J Clin Neurosci       Date:  2003-03       Impact factor: 1.961

  2 in total
  1 in total

1.  Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) and Subsequent Central Diabetes Insipidus: A Rare Presentation of Pituitary Apoplexy.

Authors:  S B Smedegaard; J O Jørgensen; N Rittig
Journal:  Case Rep Endocrinol       Date:  2019-04-02
  1 in total

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