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Intravenous immunoglobulin in lupus panniculitis.
João Espírito Santo1, M F Gomes, M J Gomes
1Departement of Medicine 1, Hospital Santa Maria, Lisbon, Portugal. joao.es@iol.pt
Systemic lupus erythematosus (SLE) skin manifestations are common, with lupus erythematosus panniculitis (LEP) being a rare form. Intravenous immunoglobulin (IVIG) shows promise in treating refractory LEP when other therapies fail.
Area of Science:
- Dermatology
- Rheumatology
- Immunology
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease with diverse systemic and cutaneous manifestations.
- Cutaneous lupus erythematosus (CLE) encompasses various skin conditions, including lupus erythematosus panniculitis (LEP), a rare subtype.
- LEP presents as recurrent nodular or plaque lesions, ranging from mild to disfiguring.
Observation:
- Standard treatments for LEP include corticosteroids, antimalarials, and azathioprine.
- Refractory cases may be managed with combination antimalarials, mycophenolate mofetil, or other immunomodulators.
- Intravenous immunoglobulin (IVIG) is utilized in various autoimmune conditions, but its efficacy in LEP lacks robust clinical trial data.
Findings:
- This report reviews SLE skin manifestations and treatment options.
- A case of LEP successfully treated with IVIG is presented.
- IVIG was effective in a patient with refractory LEP where conventional therapies were insufficient.
Implications:
- Intravenous immunoglobulin (IVIG) may represent a viable therapeutic option for recalcitrant cases of lupus erythematosus panniculitis (LEP).
- Further clinical trials are warranted to establish the efficacy and safety of IVIG for LEP.
- This case highlights the potential of IVIG in managing severe cutaneous lupus manifestations.
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