Incomplete systemic lupus erythematosus. Own observation and literature review

Autor:	T. A. Panafidina, T. V. Popkova, A. M. Lila, E. L. Nasonov
Jazyk:	ruština
Rok vydání:	2024
Předmět:	incomplete sle clinical manifestations immunological disorders therapy hydroxychloroquine Diseases of the musculoskeletal system RC925-935
Zdroj:	Научно-практическая ревматология, Vol 61, Iss 6, Pp 678-688 (2024)
Druh dokumentu:	article
ISSN:	1995-4484 1995-4492
DOI:	10.47360/1995-4484-2023-678-688
Popis:	The term of “incomplete” systemic lupus erythematosus (iSLE) is used when patients have typical clinical and immunological signs of lupus without fulfilling the classification criteria for SLE. Autoantibodies appear in patients years before diagnosis, and the most common clinical manifestations are nonspecific and may be the only symptom of the disease for some time. Progression to definite SLE occurs in 5–57% of patients with iSLE within 1–10 years. There are currently no recommendations for monitoring and treatment of iSLE patients. This article presents the results of our own research and literature analysis on clinical and pathogenetic problems of iSLE.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/7784fc51685842ab86feaa5202449588 Zobrazit plný text záznamu View record in DOAJ