Granulomatosis with Polyangiitis Presenting as Pyrexia of Unknown Origin, Leukocytosis, and Microangiopathic Haemolytic Anemia
A 66-year-old woman presented to the Emergency Department with a florid sepsis-like picture, a two-week history of fever, relative hypotension with end organ ischemia (unexplained liver enzyme and troponin elevations), and nonspecific constitutional symptoms. She was initially found to have a urinar...
Saved in:
| Main Authors: | Sima Terebelo, Iona Chen |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2017-01-01
|
| Series: | Case Reports in Rheumatology |
| Online Access: | http://dx.doi.org/10.1155/2017/6484092 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Acute Renal Failure, Microangiopathic Haemolytic Anemia, and Secondary Oxalosis in a Young Female Patient
by: Karolina M. Stepien, et al.
Published: (2011-01-01) -
A case of Hemophagocytic Lymphohistiocytosis presenting as Pyrexia of Unknown Origin
by: Indira M, et al.
Published: (2014-08-01) -
Leukocytosis of Unknown Origin: Gangrenous Cholecystitis
by: Amara Jyothi Nidimusili, et al.
Published: (2013-01-01) -
Schnitzler Syndrome: An Under-Recognised Cause of Pyrexia of Unknown Origin
by: Dennis Tin Ho Chan, et al.
Published: (2025-07-01) -
Granulomatosis with polyangiitis
by: Roberta Wartchow Machado, et al.
Published: (2025-06-01)