1 The Christ Hospital and The University of Cincinnati Medical Center, USA
2 Department of Dermatology, The University of Alabama at Birmingham, USA
Amyopathic dermatomyositis (ADM) is a rare subtype of dermatomyositis which is often recalcitrant to
immune suppressing treatments. Intravenous immunoglobulin (IVIG) has been used in the treatment of refractory
dermatomyositis. We present two patients with severe ADM, who were treated with IVIG at 2 g/kg every four weeks.
Both patients had a successful response and were able to taper the dosage of prednisone. We present both cases in
describing IVIG as a rescue and maintenance steroid-sparing agent in the treatment of severe refractory ADM. We also
review the treatment of refractory ADM with IVIg in the English literature.
Keywords: Intravenous immunoglobulin, treatment, amyopathic dermatomyositis, direct immunofluorescence.
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Intravenous Immune Globulin in Amyopathic Dermatomyositis - Report
of Two Cases and Review of the Literature
Amyopathic dermatomyositis is a rare but well described subset of dermatomyositis in which patients develop the characteristic cutaneous lesions of dermatomyositis but clinical or laboratory evidence of muscle disease is absent. As muscle disease in dermatomyositis is typically more responsive to immunomodulatory therapy than cutaneous disease, effective treatments are limited. Here we discuss two cases of refractory ADM (dermatomyositis sine myositis) that responded to IVIG as adjuvant therapy. We briefly review the evidence for the use of IVIG in adult patients with ADM and implications for therapy in the future. Search of the literature was performed with use of PubMed/MEDLINE and Google Scholar, with use of the search terms “amyopathic dermatomyositis”, “immune globulin dermatomyositis”, “IVIG dermatomyositis” and “IVIG amyopathic dermatomyositis”. The bibliography of articles found in the search was also reviewed and included if appropriate. This retrospective study was conducted after obtaining approval from the University of Alabama Institutional Review Board.
A 60 y/o woman with a past medical history significant for hypertension presented for evaluation history of pruritus and a blistering rash. A skin biopsy was performed and demonstrated subepidermal blisters with eosinophilic infiltration. Direct immunofluorescence (DIF) was weakly positive along the base while the indirect immuno-fluorescence (IIF) was positive for a net-like pemphigus pattern. The main differential diagnoses were blistering drug eruption and paraneoplastic pemphigus.
A comprehensive evaluation for occult malignancy was unremarkable, as were laboratory studies, apart from a mild eosinophilia and a positive anti-nuclear antibody (ANA), with titer 1:1280. Further autoantibody studies, including anti-SSA, anti-SSB and anti-Sm were negative and the patient was diagnosed with bullous drug eruption. Anti-hypertensive therapy was changed and a prednisone taper was initiated. The rash relapsed whenever the prednisone dose fell below 20 mg daily and dapsone (150 mg/d) was prescribed for at least eight weeks, without benefit.
She presented one year later with worsening severe pruritus and diffuse erythema over her face, back, chest, eyelids and arms, as well as plaques over the meta-carpal phalangeal (MCP), proximal intra-phalangeal (PIP) and distal intra-phalangeal (DIP) joints of both hands. She denied any other symptoms, specifically weakness, dysphagia, arthralgia or dyspnea. A skin biopsy at this time showed changes consistent with dermatomyositis. Additional laboratory evaluation was unremarkable, apart from a persistently positive ANA that remained positive. Laboratory tests including complete blood count (CBC), metabolic profile, creatinine kinase, serum protein electrophoresis (SPEP) and serum immunofixation (IFE) did not reveal any abnormalities. Tests for autoantibodies to Smith, Sjögren’s-syndrome-related antigen A and B (SSA, SSB), Jo1, Mi2 and P140 (anti-MJ) were negative.
Based on the clinical course, laboratory studies and pathology results, the patient was diagnosed with amyopathic dermatomyositis and corticosteroid sparing was begun, with an attempt to taper off prednisone. She was on each of the following systemic medications for three months without any success: mycophenolate mofetil (MMF- 2 g/d), methotrexate (15 mg/wk), and sirolimus (2 mg/d), and hydroxychloroquine (400 mg/d). Various topical corticosteroids used as adjuvant treatment provided brief temporary relief with pruritus. At this time, therapy with IVIG at a total dosage of 120 grams (2 g/kg over 3 days every 4 weeks) was initiated. Eighteen months following initiation of IVIG therapy, prednisone was tapered to 10 mg daily without a flare. Attempt to reduce the frequency of IVIG infusions to every 6 weeks resulted in a flare of skin disease that required an increase in the corticosteroid doses. At this time, her skin disease remains quiescent with IVIG infusions every 4 weeks.
A 51 year-old man presented for evaluation of intensely pruritic, erythematous plaques on both hands (MCP and PIP joints), and diffuse erythema of his chest, back and arms. He denied any systemic symptoms, including weakness, dysphagia and dyspnea. Laboratory evaluation, including CBC, metabolic profile, aldolase, creatinine kinase, ANA, SPEP, and serum IFE were within reference ranges. Autoantibodies to Smith, SSA, SSB, Jo1, Mi2, Scl70, perinuclear anti-neutrophil cytoplasmic antibodies (pANCA), cytoplasmic anti-neutrophil cytoplasmic antibodies (cANCA), anti-proteinase 3 (anti-PR3), anti-myeloperoxidase (anti-MPO) were negative. A workup for occult malignancy, including whole-body computed tomography (CT), was unremarkable. A skin biopsy was consistent with dermatomyositis.
Following this evaluation, therapy with prednisone 60mg daily was initiated. Attempts to taper the prednisone below 40 mg/day were unsuccessful, despite the use of azathioprine 150 mg/day and hydroxychloroquine 400 mg/day. In addition to the erythematous plaques described above, he developed several painful, draining non-healing ulcers on his feet and buttocks. Treatment with IVIG at total dosage of 160 grams (2g/kg over 4 days every 4 weeks) was initiated and within 12 weeks, improvements were noted in the rash and ulcers. The prednisone was tapered to 20 mg/day without any flare in his skin disease.
Following the prednisone taper, he developed severe Raynaud’s phenomenon that did not respond to treatment with oral nifedipine and pentoxifylline as well as topical nitroglycerine. He did have a good response to local botulinum toxin in all digits except his index finger, which required partial amputation due to persistent ischemia.
After eight months, the IVIG dose interval was increased to every 6 weeks since his cutaneous disease was well controlled. Shortly after the IVIG interval was increased, he developed spontaneous pneumomediastinum and was diagnosed with interstitial lung disease. The IVIG dose interval was decreased to every 4 weeks and 4 doses of rituximab at 375 mg/m2 were given.
At follow-up one year after the rituximab and IVIG dose-adjustment, he has had resolution of his cutaneous disease (rash and ulcers) and improvement of his ILD. He has had no further pneumomediastinum or flares of Raynaud’s. He is currently stable on prednisone 5 mg/day, azathioprine 150 mg/day and hydroxychloroquine 400mg/ day.
Dermatomyositis is a humoral inflammatory disease, with an antibody and complement mediated necrotizing vasculopathy though it is thought that Toll-like receptors (TLR) and type 1 interferon also are involved in pathogenesis [1Dalakas MC, Hohlfeld R. Polymyositis and dermatomyositis Lancet 2003; 362: 971-82. [http://dx.doi.org/10.1016/S0140-6736(03)14368-1] , 2Gherardi RK. Pathogenic aspects of dermatomyositis, polymyositis and overlap myositis Presse Med 2011; 40: e209-18. [http://dx.doi.org/10.1016/j.lpm.2010.12.013] ]. This is in contrast with polymyositis, which is generally understood to be that of a cellular inflammatory process, primarily mediated by CD8+ T lymphocytes [1Dalakas MC, Hohlfeld R. Polymyositis and dermatomyositis Lancet 2003; 362: 971-82. [http://dx.doi.org/10.1016/S0140-6736(03)14368-1] ].
Dermatomyositis can occur as an idiopathic process, as an association with malignancy, as a drug reaction or in association with another connective tissue disease [3Callen JP. Dermatomyositis Lancet 2000; 355: 53-7. [http://dx.doi.org/10.1016/S0140-6736(99)05157-0] ]. Additionally, dermatomyositis can be complicated by ulcerated skin lesions [4Shimojima Y, Ishii W, Kato T, et al. Intractable skin necrosis and interstitial pneumonia in amyopathic dermatomyositis, successfully treated with cyclosporin A Intern Med 2003; 42: 1253-8. [http://dx.doi.org/10.2169/internalmedicine.42.1253] ] or interstitial lung disease, which is often associated with poor prognosis [5Neuhaus IM, Connolly MK. An unusual presentation of amyopathic dermatomyositis associated with fatal interstitial lung disease Arch Dermatol 2006; 142: 113-4. [http://dx.doi.org/10.1001/archderm.142.1.113] ].
The therapeutic approach in dermatomyositis is based on the presence or absence of muscular involvement. Since our patients did not report or demonstrate any clinical symptoms or signs of muscle disease on physical examination and creatine kinase assay was within normal limits, further involvement of muscle disease was not tested. In classical DM, initial therapy consists of 1mg/kg prednisone (or equivalent) daily that is continued for at least 6 weeks after clinical and biochemical remission is achieved. Steroid therapy will result in remission of muscle disease in 75% of patients. The remaining patients require the addition of an additional immunosuppressive agent such as azathioprine, mycophenolate or methotrexate [6Callen JP, Wortmann RL. Dermatomyositis Clin Dermatol 2006; 24: 363-73. [http://dx.doi.org/10.1016/j.clindermatol.2006.07.001] ]. The cutaneous findings are often more refractory to therapy and frequently do not respond to corticosteroids [6Callen JP, Wortmann RL. Dermatomyositis Clin Dermatol 2006; 24: 363-73. [http://dx.doi.org/10.1016/j.clindermatol.2006.07.001] ]. As such, an alternative approach to immunosuppressive therapy such as intravenous immune globulin is often required.
In Tables 1 and 2, we summarize the published English-language literature regarding IVIG in amyopathic dermatomyositis from Japan, Spain, France, and the United States which were between the years 2009-2013. Table 2 is separate because of a different degree of detail in the reported cases. In Table 2, the treatment course of IVIG was 2gm/kg, given as 1gm/kg every two days and was repeated every three to four weeks. Cases of paraneoplastic amyopathic dermatomyositis were not included.
Demographics, Clinical response and follow-up to IVIg treatment.
Baseline characteristics of this population are summarized belo.: All data are from Bonfour et al. .
Clinical response and follow-up treatment are summarized below:
The cases reviewed show that IVIG in adults is effective as in amyopathic dermatomyositis refractory to standard immunosuppressive regimens. In our review of IVIG as salvage therapy, 35 of 43 patients with amyopathic DM had at least a partial response and 26 of 43 had a significant (complete or nearly complete) response. Additionally, 2 of 6 with concomitant interstitial lung disease had a good clinical response. We believe this is significant, as all had failed to respond to previous intensive immunosuppressive regimens, including systemic glucocorticoids, calcineurin inhibitors and antimetabolites such as azathioprine, mycophenolate and cyclophosphamide. Although the small numbers of patients and the significant population heterogeneity does not allow us to draw definitive conclusions, we believe that the use of IVIG can be considered as adjuvant therapy in amyopathic DM refractory to conventional oral treatments.
Immune globulin therapy has the additional benefit of acting as an immunomodulatory agent rather than an immunosuppressive agent. The mechanism of action is incompletely understood, but is believed to include inhibition of antibody activity and suppression of inflammatory cytokine secretion [12Gelfand EW. Intravenous immune globulin in autoimmune and inflammatory diseases N Engl J Med 2012; 367: 2015-25. [http://dx.doi.org/10.1056/NEJMra1009433] ]. Of particular interest, IVIG has been noted to have efficacy in steroid-resistant cases and has demonstrated efficacy in treatment of dermatomyositis [13Dalakas MC, Illa I, Dambrosia JM, et al. A controlled trial of high-dose intravenous immune globulin infusions as treatment for dermatomyositis N Engl J Med 1993; 329: 1993-2000. [http://dx.doi.org/10.1056/NEJM199312303292704] ]. Although expensive, its costs should be balanced with the long-term adverse effects of steroids, antimetabolites and calcineurin inhibitors. Additional adverse effects of IVIG include nephrotoxicity with high or repeated doses, however newer formulations appear to have a reduced incidence of renal toxicity, which make this a more appealing option [14Chapman SA, Gilkerson KL, Davin TD, Pritzker MR. Acute renal failure and intravenous immune globulin: occurs with sucrose-stabilized, but not with D-sorbitol-stabilized, formulation Ann Pharmacother 2004; 38: 2059-67. [http://dx.doi.org/10.1345/aph.1E040] ].
Both our cases support the use of IVIG for ADM that is refractory to standard therapy, both with and without interstitial lung disease. Further data is needed to better understand the role and timing of IVIG in therapy of ADM.
CONFLICT OF INTEREST
The authors confirm that this article content has no conflict of interest.
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Penate Y, Guillermo N, Melwani P, Martel R, Hernandez-Machin B, Borrego L. Calcinosis cutis associated with amyopathic dermatomyositis: response to intravenous immunoglobulin J Am Acad Dermatol 2009; 60: 1076-7. [http://dx.doi.org/10.1016/j.jaad.2008.09.051]
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Femia AN, Eastham AB, Lam C, Merola JF, Qureshi AA, Vleugels RA. Intravenous immunoglobulin for refractory cutaneous dermatomyositis: a retrospective analysis from an academic medical center J Am Acad Dermatol 2013; 69: 654-7. [http://dx.doi.org/10.1016/j.jaad.2013.06.007]
Bounfour T, Bouaziz JD, Bezier M, et al. Clinical efficacy of intravenous immunoglobulins for the treatment of dermatomyositis skin lesions without muscle disease J Eur Acad Dermatol Venereol 2014; 28(9): 1150-7. [http://dx.doi.org/10.1111/jdv.12223]
Dalakas MC, Illa I, Dambrosia JM, et al. A controlled trial of high-dose intravenous immune globulin infusions as treatment for dermatomyositis N Engl J Med 1993; 329: 1993-2000. [http://dx.doi.org/10.1056/NEJM199312303292704]
Chapman SA, Gilkerson KL, Davin TD, Pritzker MR. Acute renal failure and intravenous immune globulin: occurs with sucrose-stabilized, but not with D-sorbitol-stabilized, formulation Ann Pharmacother 2004; 38: 2059-67. [http://dx.doi.org/10.1345/aph.1E040]