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"Half-half" blisters in bullous pemphigoid successfully treated with adjuvant high-dose intravenous immunoglobulin.
Acta Dermatovenerol Alp Pannonica Adriat
September 2012
Serviço de Dermatologia, Hospital de Santa Maria-Centro Hospitalar Lisboa Norte Avenida Prof. Egas Moniz, Lisbon, Portugal.
Bullous pemphigoid is a rare, autoimmune blistering disease. Its clinical presentation is tense blisters that may arise on normal-appearing or erythematous skin. Bullous pemphigoid refractory to systemic corticosteroids in combination with immunosuppressants such as azathioprine and mycophenolate mofetil may benefit from adjuvant high-dose intravenous immunoglobulin (IVIg).
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