| Literature DB >> 32817738 |
Barnali Das1, Rekha Khaund Borkotoky1, Amrit Lal Saha1, Geetanjali Sahariah Khound1, Puja Banerjee Barua1, Siba Prosad Paul2.
Abstract
Systemic lupus erythematosus (SLE) is an autoimmune multisystem disease. Childhood-onset SLE is extremely rare and comprises only 10% to 20% of all cases. In this case report, we present a 9-year-old boy from northeastern India who presented with fever, cough, vague abdominal pain, lethargy and swelling of face and legs. Initial impression was one of sepsis with central nervous system (CNS) involvement and was treated accordingly. Detailed clinical examination with subsequent laboratory and imaging studies clinched the diagnosis of SLE. The patient showed rapid resolution of symptoms with immunoglobulins, cyclophosphamide and steroid therapy. A brief discussion on childhood neuropsychiatric lupus syndrome and SLE with CNS infections is included here.Entities:
Keywords: Children; Neurological manifestations; Neuropsychiatric systemic lupus erythematosus; Resource-limited settings; Sepsis; Systemic lupus erythematosus
Year: 2020 PMID: 32817738 PMCID: PMC7423309 DOI: 10.24911/SJP.106-1565526532
Source DB: PubMed Journal: Sudan J Paediatr ISSN: 0256-4408