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Recalcitrant pemphigus vulgaris: aseptic meningitis associated with intravenous immunoglobulin therapy and successful treatment with rituximab
Author(s) -
Ventura Filipa,
Rocha Joana,
Fernandes José Carlos,
Machado Álvaro,
Brito Celeste
Publication year - 2013
Publication title -
international journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 93
eISSN - 1365-4632
pISSN - 0011-9059
DOI - 10.1111/j.1365-4632.2010.04870.x
Subject(s) - medicine , aseptic meningitis , rituximab , pediatrics , antibody , meningitis , immunology
successful treatment with rituximab Dear Sir, We report the case of a 26-year-old woman with a 5-year history of a severe and recalcitrant pemphigus vulgaris (PV) (Fig. 1). During this period, the patient was treated with prednisolone, first combined with azathioprine and later with mycophenolate mofetil, but without complete response and always worsening when prednisolone tapering was attempted. In this setting, she was treated with intravenous immunoglobulin (IVIG) (2 g/kg over three days) in combination with prednisolone (40 mg/d). On the third day of IVIG, she presented with severe headache, nuchal rigidity, photophobia, and nausea. Neurological examination was otherwise normal as was the brain computed tomography scan. Lumbar puncture was performed, and the cerebrospinal fluid predominantly showed a raised white cell lymphocyte count (80/ll) with normal glucose and protein contents. Cerebrospinal fluid culture and polymerase chain reaction for common viruses were both negative. These findings supported the diagnosis of aseptic meningitis secondary to immunoglobulin infusion. She recovered over the next 48 hours without any medication, and she was discharged after four days. The PV continued to worsen with numerous active lesions mostly on the scalp, face, back, and oral mucosa. Cyclosporine in association with prednisolone and mycophenolate mofetil had no benefit. Finally, rituximab 375 mg/m IV weekly, over four consecutive weeks, was tried. After the second infusion, lesions began to heal, with complete re-epithelization two months after treatment. No relevant side effects were reported. After one year, the patient is doing well, without lesions (Fig. 2). It should be noted in this case the occurrence of aseptic meningitis as a serious side effect of treatment with IVIG and the good response to rituximab. In fact, IVIG therapy is widely used in autoimmune diseases and usually recognized as a safe biologic agent. Aseptic meningitis is one of the uncommon severe adverse reactions of IVIG therapy. The incidence ranges from 11% to 17%. The mechanism for IVIG-induced aseptic meningitis is not well understood. Studies showed that severe adverse events might be minimized by enforcing a slow administration rate and adequate hydration. Rituximab results in the depletion of normal as well as malignant B cells, leading to investigation of its use in autoimmune disorders, particularly in the treatment of systemic lupus erythematosus and rheumatoid arthritis. Although there have been no randomized controlled trials of rituximab in dermatologic disease, case reports describe its use in PV, paraneoplastic pemphigus, epidermolysis bullosa acquisita, cutaneous B-cell lymphoma, dermatomyositis, graft-versus-host disease, Wegener’s granulomatosis, microscopic polyangiitis, cryoglobulinemic vasculitis, and Churg–Strauss syndrome. 501 (a)