Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) and Subsequent Central Diabetes Insipidus: A Rare Presentation of Pituitary Apoplexy
Pituitary apoplexy (PA) is a rare endocrine emergency that occasionally presents with sodium disturbances. Here we present a rare case with a previously healthy 41-year-old female who presented with acute onset headache and nausea without visual impairment or overt pituitary dysfunction. Plasma sodi...
Saved in:
| Main Authors: | S. B. Smedegaard, J. O. Jørgensen, N. Rittig |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2019-01-01
|
| Series: | Case Reports in Endocrinology |
| Online Access: | http://dx.doi.org/10.1155/2019/7592648 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Case report: a rare mediastinal neuroblastoma in an adult associated with syndrome of inappropriate secretion of antidiuretic hormone (SIADH)
by: Caio Silvério de Souza, et al.
Published: (2023-08-01) -
Severe hyponatremia and the syndrome of inappropriate secretion of antidiuretic hormone (SIADH) associated with fluoxetine: case report
by: Carlos Alexandre Twardowschy, et al.
Published: (2006-03-01) -
Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) akibat Kemoterapi pada Pasien Lansia dengan Keganasan
by: Velma Herwanto, et al.
Published: (2014-07-01) -
Quetiapine-Induced Syndrome of Inappropriate Secretion of Antidiuretic Hormone
by: Theocharis Koufakis
Published: (2016-01-01) -
Docetaxel-induced syndrome of inappropriate antidiuretic hormone secretion
by: Tamojit Chaudhuri, et al.
Published: (2013-01-01)