Lupus Myelopathy in a Child

• Author(s): Vieira, JP ; Ortet, O ; Barata, D ; Abranches, M ; Gomes, JM
• Date: 2002
• Persistent ID: http://hdl.handle.net/10400.17/68
• Origin: Repositório do Centro Hospitalar de Lisboa Central, EPE
• Subject(s): Criança; Lúpus Eritematoso; Ressonância Magnética; Mielopatia; HDE PED; HDE UCI PED; HDE NEU PED
• Document Type: Article

Description

A 5-year-old female developed, after a 7-month period of fever, anorexia, weight loss, and a transitory cutaneous erythematous eruption, a severe acute transverse myelopathy, with a partial recovery of motor and sensory function. She had positive antinuclear and antidouble-stranded DNA antibodies but no antiphospholipid antibodies. Six months later she had massive proteinuria and restarted treatment with steroids and cyclophosphamide. Our patient is one of the youngest reported with lupus myelopathy. We discuss the clinical presentation, the magnetic resonance imaging findings, and other relevant laboratory studies of this rare but serious complication of systemic lupus erythematosus.