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Rhupus syndrome. a case report of a rare combination.

作者信息

Drie Tasneem, Khalayli Naram, Haidar Ghina, Haj Ali Diaa

机构信息

Faculty of Medicine, Damascus University, Damascus.

Syrian Private University, Daraa, Syria.

出版信息

Ann Med Surg (Lond). 2023 Nov 16;86(1):535-538. doi: 10.1097/MS9.0000000000001517. eCollection 2024 Jan.

Abstract

INTRODUCTION AND IMPORTANCE

Rhupus syndrome is a very rare combination of systemic lupus erythematosus and rheumatoid arthritis. It is characterized by the presence of erosive arthritis with symptoms and signs of systemic lupus erythematosus. Rheumatoid nodules and neurological and renal involvement are further complications of Rhupus syndrome, leading to a worse prognosis.

CASE PRESENTATION

The authors presented a young female patient diagnosed with lupus erythematosus, who laterally, developed clinical signs and biomarkers that led to the diagnosis of Rhupus syndrome. This is believed to be of relevance to the knowledge of the medical community.

CONCLUSION

Despite being a rare entity, it is important to know its early diagnosis, and treatment to reduce the complications.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ee/10783322/126b9d04c291/ms9-86-535-g001.jpg

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