Case report highlights neurologic and neuropsychiatric complications in childhood systemic lupus erythematosus, suggesting the need for interdisciplinary management.
Background Systemic lupus erythematosus (SLE) is an autoimmune, multisystem disorder with diverse manifestations. There are limited reports on the neuro‐ophthalmic and neuropsychiatric findings in childhood SLE. Case Report An 8‐year‐old patient with suspected SLE with a history of skin rash, joint pain, transient hematologic abnormality, headaches, seizures, and psychosis, presented with papilledema secondary to acquired, obstructive hydrocephalus. Discussion SLE‐related ocular and neuropsychiatric findings are reviewed. Proposed mechanisms for ocular and cerebral lupus include immune complex deposition, vascular thrombosis, and postinflammatory lesions. Conclusion The prevalent neurologic and neuropsychiatric complications of pediatric SLE require close follow‐up and interdisciplinary management.
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Daisy Q. Chan (2000) studied this question.
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