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Drug-Induced Pemphigus: A Systematic Review of 170 Patients Publisher Pubmed



Ghaedi F1 ; Etesami I1 ; Aryanian Z1, 2 ; Kalantari Y1 ; Goodarzi A3 ; Teymourpour A4 ; Tavakolpour S1, 5 ; Mahmoudi H1 ; Daneshpazhooh M1
Authors
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Authors Affiliations
  1. 1. Autoimmune Bullous Diseases Research Center, Tehran University of Medical Sciences, Tehran, 009821, Iran
  2. 2. Department of Dermatology, Babol University of Medical Sciences, Babol, 0098111, Iran
  3. 3. Dermatology School of Medicine Iran University of Medical Sciences, Tehran, 009821, Iran
  4. 4. Department of Epidemiology and biostaristics, school of public health, Tehran university of medical sciences, Tehran, 009821, Iran
  5. 5. Dana-Farber Cancer Institute, Harvard Medical School, Boston, 02215, MA, United States

Source: International Immunopharmacology Published:2021


Abstract

Pemphigus encompasses a rare heterogeneous group of autoimmune blistering diseases characterized by cutaneous and/or mucosal blistering. Multiple factors, such as some specific types of drugs, have been found to be involved in the induction of pemphigus. Here, we have designed a systematic review by searching PubMed/Medline and Embase databases to find the drugs, involved in pemphigus induction and exacerbation (updated on 19 August 2019). From 856 initially found articles, 134 studies (198 patients; 170 patients in the drug-induced patients and 28 in exacerbation group) have been included. Regarding drug-induced cases, the mean age was 57.19 ± 16.9-year-old (ranged 8–105), and patients had developed pemphigus within a mean of 154.27 days. Pemphigus vulgaris (38.9%), pemphigus foliaceus (33.5%), and paraneoplastic pemphigus (3.6%) were the most common subtypes. Furthermore, penicillamine (33.1%), captopril (7.7%), and bucillamine (6.5%) were the most reported drugs related to pemphigus induction; penicillamine was associated with the most persistent disease. Regardless of disease subtype, cutaneous, mucocutaneous, and mucosal involvements were reported in 68.6%, 30.1%, and 1.3% of patients, respectively. In total, the IgG deposition in the pathological studies, being positive for autoreactive antibodies in the serum against desmoglein 3 (Dsg3), and desmoglein 1 (Dsg1), were reported in 93%, 34.9%, and 72.7% of reported patients, respectively. Regarding the management of such patients, in 75% of healed cases, treatment (mainly transient systemic and topical corticosteroids and/or azathioprine) was needed besides stopping the probable pemphigus-inducing culprit drug, while drug cessation was enough to control the disease in 25%. As the outcomes, the lesions in 129 of 147 (87.8%) patients had been healed, while in 18 (12.2%), no healing was reported; fifteen out of 18 had died. In conclusion, some specific groups of treatments can induce pemphigus, including penicillamine, captopril, and bucillamine; despite the similar clinical and pathological manifestations to classical pemphigus, most of the cases are less severe and have a better prognosis. © 2020 Elsevier B.V.
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