A case of "scleroderma renal crisis" developed from diffuse scleroderma.
- Author:
Jeong Bae JEON
1
;
Wha Sook KIM
;
Kun Ho KWON
;
Seoung Woo LEE
;
Moong Jae KIM
;
Won PARK
Author Information
1. Department of Internal Medicine, Inha University, College of Medicine, Inchon, Korea.
- Publication Type:Case Report
- Keywords:
Scleroderma renal crisis;
Hemodialysis;
ACE inhibitor
- MeSH:
Autoimmune Diseases;
Biopsy;
Humans;
Kidney;
Muscle Weakness;
Muscle, Skeletal;
Polymyositis;
Recurrence;
Renal Dialysis;
Renal Insufficiency;
Rhabdomyolysis;
Scleroderma, Diffuse*
- From:Korean Journal of Medicine
1999;56(5):646-651
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Polymyositis is an inflammatory, autoimmune disease of the skeletal muscle characterized by symmetrical, proximal muscle weakness, elevated muscle enzymes, and characteristic features on electromyogram and muscle biopsy. The kidneys are generally spared and myoglobinuric renal failure is very rare in polymyositis. There have been infrequent reports of polymyositis developing myoglobinuric renal failure secondary to rhabdomyolysis. The flare-up may occur in polymyositis, usually manifest within several weeks to months of achieving a remission. But, rhabdomyolysis and myoglobinuric renal failure was a very rare feature of the relapse of polymyositis. We present a case report of patient with polymyositis who initially presented and relapsed as rhabodomyolysis that lead to myoglobinuric, oliguric renal failure and required transient dialytic support.
