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The Mystery of IVIg


An 11-year-old Caucasian female with juvenile dermato­myositis (JDMS) presented to our clinic with a worsening rash and increased proximal muscle weakness. Three years prior to this visit, the patient had been diagnosed with JDMS based on clinical presentation, elevated muscle enzymes, and characteristic findings on muscle biopsy and electromyography. She was successfully managed with chronic oral corticosteroids and weekly oral methotrexate.


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English
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https://www.the-rheumatologist.org/article/the-mystery-of-ivig/
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