Rhupus syndrome. a case report of a rare combination

Author:

Drie Tasneem1,Khalayli Naram1,Haidar Ghina1,Haj Ali Diaa2

Affiliation:

1. Faculty of Medicine, Damascus University, Damascus

2. Syrian Private University, Daraa, Syria

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

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Surgery

Reference10 articles.

1. A case of rhupus-reporting of a rare entity;Sinha;Indian Dermatol Online J,2019

2. A rare case of rhupus syndrome with systemic involvement: a case report and literature review;Dairi;Cureus,2022

3. Rhupus syndrome. A rare combination;Cartas;Revista Colombiana de Reumatol,2017

4. Rhupus syndrome: overlap of rheumatoid arthritis and systemic lupus erythematosus;Hussain;Austin J Clin Immunol,2021

5. The SCARE 2020 guideline: updating consensus Surgical Case Report (SCARE) guidelines;Agha;Int J Surg,2020

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