- Letter to the Editor
- Open Access
Systemic retinoids for treatment of recalcitrant IgA pemphigus
Orphanet Journal of Rare Diseases volume 13, Article number: 163 (2018)
IgA pemphigus is an exceedingly rare autoimmune blistering disorder, caused by IgA autoantibodies against desmosomal proteins. No treatment option has been found to be universally effective. The disease is often recalcitrant to oral steroids and immunosuppressants. Here, we describe the use of systemic retinoids for the treatment of recalcitrant IgA pemphigus in 3 cases. Although the use of acitretin has been reported before, we present for the first time the positive effects of alitretinoin in treatment of 2 patients with IgA pemphigus. Besides hyperlipoproteinaemia requiring use of hypolipidemic agents in one case, alitretinoin was well-tolerated and has generally a more favorable side effect spectrum than immunosuppressants.
IgA pemphigus is an autoimmune blistering disorder, caused by IgA autoantibodies against keratinocyte cell surface antigens, desmocollins 1–3 and sometimes desmogleins 1 and 3. Based on clinical and histopathological characteristics it can be subdivided into subcorneal dermatosis type (SPD) and intraepidermal neutrophilic type (IEN) [1, 2] The patients present with flaccid pustules solely or on scaly erythematous plaques, often arranged in an annular or circinate pattern [3, 4], which are commonly itchy and located on the trunk. No treatment option has been found to be universally effective. The disease is often recalcitrant to local and/ or oral steroids and immunosuppressants . Given the extreme rarity of the disease no controlled treatment trials exist or are likely to be conducted. We describe the novel use of alitretinoin in two out of three of our IgA pemphigus patients as a steroid-sparing agent.
Patients and methods
Over the last 10 years we cared for three female patients with IgA pemphigus, with disease presenting around the age of 60 (Fig. 1). The diagnostic analyses performed are summarized in Table 1 and Additional file 1: Figure S1. Two of them have an underlying monoclonal gammopathy of undetermined significance (MGUS). Bence Jones light chains are negative. In the other case an underlying haematological condition or other malignancy was excluded. Interestingly, all three patients had a recalcitrant disease with at least four immunosuppressive or immunomodulatory drugs given, resulting in unsatisfactory response and/ or accompanied by intolerable side effects (Table 1). Besides local steroids the following treatments were used: dapsone, azathioprine, mycophenolate mofetil, colchicine, prednisolone, methotrexate, anakinra, cyclosporine and cyclophosphamide. In all three patients we initiated treatment with acitretin at dosage of 10–30 mg, which has been reported before to be effective in a few cases .
Results and discussion
The treatment with the retinoid acitretin in all three patients resulted in a satisfactory, at least partial disease response. In two out of three cases, however, side effects (dizziness, hair loss and severe mucosal xerosis) occurred, prompting switch to the retinoid alitretinoin, which was given at a dosage of 30 mg daily. Alitretinoin is a novel systemic, endogenous retinoid acting as a pan-agonist for the nuclear retinoid receptors retinoic acid receptor (RAR) and retinoid-X-receptor (RXR). It is the first systemic treatment to be approved in the EU for patients with severe chronic hand eczema unresponsive to potent topical corticosteroids. It has also been used in pilot studies for other chronic inflammatory skin disorders . Besides hyperlipoproteinaemia requiring use of hypolipidemic agents in one of our patients – one of the most commonly reported side-effect of alitretinoin  – the drug was well-tolerated and has a favourable side effect spectrum compared to immunosuppressants. This is specifically important in light of the increased risk for malignancies, observed in patients with IgA pemphigus [2, 9].
Our observations suggest that due to their antiinflammatory and antiproliferative functions, systemic retinoids and especially alitretinoin represent an excellent treatment option for IgA pemphigus, an exceedingly rare autoimmune blistering skin disease, which is commonly recalcitrant to different treatment options .
monoclonal gammopathy of undetermined significance
retinoic acid receptor
Hashimoto T, Teye K, Ishii N. Clinical and immunological studies of 49 cases of various types of intercellular IgA dermatosis and 13 cases of classical subcorneal pustular dermatosis examined at Kurume University. Br J Dermatol. 2017;176:168–75.
Geller S, Gat A, Zeeli T, Hafner A, Eming R, Hertl M, et al. The expanding spectrum of IgA pemphigus: a case report and review of the literature. Br J Dermatol. 2014;171:650–6.
Kiritsi D, Hoch M, Kern JS. Annular flaccid pustules on the trunk. JAMA Dermatol. 2017;153:921–2.
Tsuruta D, Ishii N, Hamada T, Ohyama B, Fukuda S, Koga H, et al. IgA pemphigus. Clin Dermatol. 2011;29:437–42.
Moreno ACL, Santi CG, Gabbi TVB, Aoki V, Hashimoto T, Maruta CW. IgA pemphigus: case series with emphasis on therapeutic response. J Am Acad Dermatol. 2014;70:200–1.
Bellissen A, Lebas D, Wantz M, Gosset P, Lasek A, Modiano P. Efficacy of acitretin in IgA pemphigus. Ann Dermatol Venereol. 2013;140:793–6.
Blair HA, Scott LJ. Alitretinoin: a review in severe chronic hand eczema. Drugs. 2016;76:1271–9.
Diepgen TL, Pfarr E, Zimmermann T. Efficacy and tolerability of alitretinoin for chronic hand eczema under daily practice conditions: results of the TOCCATA open study comprising 680 patients. Acta Derm Venereol. 2012;92:251–5.
España A, Gimenez-Azcarate A, Ishii N, Idoate MA, Panizo C, Hashimoto T. Antidesmocollin 1 autoantibody negative subcorneal pustular dermatosis-type IgA pemphigus associated with multiple myeloma. Br J Dermatol. 2015;172:296–8.
We thank the patients and their families, as well as other treating dermatologists in the Department of Dermatology, Medical Center-University of Freiburg, Freiburg, Germany.
DK’s work has been supported by the Mathilde-Wagner-Habilitationspreis from the University of Freiburg.
Availability of data and materials
Data sharing not applicable to this article as no datasets were generated or analysed during the current study.
Ethics approval and consent to participate
Not applicable (off-label treatment with systemic retinoids as part of compassionate use in an extremely rare disease).
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Has been obtained.
The authors declare that they have no competing interests.
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Figure S1. Haematoxylin-eosin stainings of patients’ biopsies, as well as direct immunofluorescence staining pictures with IgA for diagnostics are shown. Both the histological and the immunofluorescence findings are similar in the 3 cases. The histology shows spongiosis and intraepidermal blisters, as well as infiltrates of neutrophilic granulocytes (hematoxylin-eosin, original magnification × 100). Direct immunofluorescence microscopy revealed IgA deposits at the upper part of the epidermis (original magnification × 200). (TIF 548 kb)
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Schauer, F., Kern, J.S. & Kiritsi, D. Systemic retinoids for treatment of recalcitrant IgA pemphigus. Orphanet J Rare Dis 13, 163 (2018). https://doi.org/10.1186/s13023-018-0899-y
- Autoimmune skin blistering