Langerhans Cell Histiocytosis Manifests with Acute Severe Hypernatremia during Hospitalization
Central diabetes insipidus (DI) is characterized by a deficiency in arginine vasopressin (AVP), an antidiuretic hormone leading to excessive free water loss in the urine and hypernatremia. Central DI can be the first presentation of several occult diseases. However, patients with central DI who have...
Saved in:
Main Authors: | Kullaya Takkavatakarn, Hansamon Poparn, Pisut Katavetin |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2022-01-01
|
Series: | Case Reports in Nephrology |
Online Access: | http://dx.doi.org/10.1155/2022/6120644 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Rare Case of Erdheim-Chester Disease (Non-Langerhans Cell Histiocytosis) with Concurrent Langerhans Cell Histiocytosis: A Diagnostic and Therapeutic Challenge
by: Hamza Hashmi, et al.
Published: (2018-01-01) -
Rare Lung Diseases III: Pulmonary Langerhans’ Cell Histiocytosis
by: Stephen C Juvet, et al.
Published: (2010-01-01) -
An Aggressive Form of Langerhan Cell Histiocytosis in an Adult: Therapeutic Challenges
by: Karan Seegobin, et al.
Published: (2017-01-01) -
Langerhans Cell Histiocytosis: A Diagnostic Challenge in the Oral Cavity
by: Mehmet Ali Altay, et al.
Published: (2017-01-01) -
Pulmonary Langerhans Cell Histiocytosis and Diabetes Insipidus in a Young Smoker
by: K. Earlam, et al.
Published: (2016-01-01)