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- Title
Scabies, incomplete lupus erythematosus and Henoch-Schonlein purpura.
- Authors
Yang Fang Wu; Jing Jing Wang; Hui Hui Liu; Wei Xia Chen; Peng Hu; Wu, Yang Fang; Wang, Jing Jing; Liu, Hui Hui; Chen, Wei Xia; Hu, Peng
- Abstract
ILE patients had at least one but less than four of the ACR classification criteria of SLE and did not present distinctive clinical features or meet classification criteria of other connective tissue diseases [4]. Clinical and serologic features in patients with incomplete lupus classification versus systemic lupus erythematosus patients and controls. ILE patients have at least one but less than four of the American College of Rheumatology (ACR) classification criteria of systemic lupus erythematosus (SLE) and do not present distinctive clinical features or meet classification criteria of other connective tissue diseases [4]. Although the majority of ILE patients may never reach SLE classification, about 10-50% of ILE patients are at high risk of progressing to complete SLE within 5 years [10].
- Subjects
SCABIES; LUPUS erythematosus; HIV antibodies
- Publication
Archives of Medical Science, 2021, Vol 17, Issue 2, p564
- ISSN
1734-1922
- Publication type
journal article
- DOI
10.5114/aoms/131542