Bullous pemphigoid (BP) is the most common autoimmune blistering disease of the skin and mucous membranes. 1,2 Although autoantibodies targeting proteins of the dermoepidermal junction (BP antigen 1 (BPAG1/ BP230) and BP antigen 2 (BPAG2/ BP180)) have been demonstrated as the physiopathological bases of BP, 1,3 the exact pathogenesis remains unknown.Reported annual incidence of BP varies 3-5 and ranges from 2.4 to 21.7 per million population. However, the tendency for BP incidence to increase is clear-cut. 4,[6][7][8] This increase has been attributed to population ageing, drug-induced cases and improvement in the diagnosis due to increasing awareness of non-bullous and atypical variants of BP. 1,3,8 Many studies have corroborated the potential association of medication use with BP. 9-12 Dipeptidyl peptidase-4 inhibitors
Intralesional methotrexate (il-MTX) has been reported as a useful therapy in keratoacanthoma (KA) and cutaneous squamous cell carcinoma (cSCC). However, the data available on the histological changes induced by this therapy are very scarce. We conducted a single center, prospective study that included 65 cases of cSCC treated with il-MTX before surgical treatment. Two histological studies were conducted in all patients: before intralesional treatment and after surgical removal. Lesions were assessed longitudinally both clinically and histologically. 60 patients (92.3%) responded to il-MTX treatment. There were no differences regarding aggressive histological features of the cSCC between responder and non-responder patients. All cases showed a chronic inflammatory infiltrate after il-MTX. Intratumoral necrosis areas were frequently observed. All cases showed local fibrosis with fine thickening of collagen bundles. Il-MTX induces a chronic lymphohistiocytic inflammatory reaction in both clinical responder and nonresponder patients. Tumor involution after il-MTX is followed by a fine fibrosis that explains the great cosmetic results and improves the accuracy of the follow-up.
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