Severe Thrombocytopenia as the Main Manifestation of Childhood-Onset Systemic Lupus Erythematosus.

Abstract

Thrombocytopenia is a common hematologic abnormality of childhood-onset systemic lupus erythematosus (cSLE). Although in most cases thrombocytopenia is mild, severe thrombocytopenia with bleeding complications might occur, and is further correlated with disease activity and a worse prognosis. We report two female patients with severe thrombocytopenia as the initial manifestation of cSLE, which were successfully treated by intensive immunosuppression including several high-dose methylprednisolone pulses and IV cyclophosphamide. Both patients were initially diagnosed with idiopathic thrombopenic purpura (ITP) refractory to conventional treatment and complicated with haemorrhagic manifestations. For this matter, patients with ITP should be assessed for the presence of ANA, anti-dsDNA antibodies, and complement levels, since they are at high risk to develop cSLE.

• Authors: Cristian Quintana-Ortega, Agustín Remesal, Ana Pérez Vigara, Manuel Parrón-Pajares, Montserrat Bret, Rosa Alcobendas, Sara Murias
• Journal: Mediterranean journal of rheumatology (Mediterr J Rheumatol) Vol. 33 Issue 4 Pg. 459-464 (Dec 2022) ISSN: 2529-198X [Electronic] Greece
• PMID: 37034366 (Publication Type: Case Reports)
• Copyright: © 2022 The Mediterranean Journal of Rheumatology (MJR).