Aggressive Kaposi’s Sarcoma Associated With Golimumab Therapy
Özet
A 65-year-old male patient with a 25-year history of psoriasis and psoriatic arthritis presented to our clinic. He described the onset of new lesions three weeks ago (Figure 1). His dermatologic examination revealed purple plaque and nodules on the anterior and posterior trunk and extremities. One month ago, his examination was performed again in our clinic, and these lesions were absent. Patient's detailed medical history revealed prior use of both conventional and novel anti-tumor necrosis factor-alpha (anti-TNF-α) treatments (methotrexate 15 mg-20 mg/week for four years, etanercept 50 mg/week for two years, adalimumab 40 mg every two weeks for two years, and infliximab 5 mg/kg in usual regimen for two years). Because of refractory psoriatic arthritis; golimumab (50 mg/month subcutaneous) was started after two years of the biologic drug-free period. In a few months, patient’s arthritic complaints resolved; psoriatic plaques diminished. He had received three doses of the drug when multiple purplish macules and plaques had appeared. Skin biopsy was performed from two plaques on the left toe and abdomen. Histopathological examination was consistent with Kaposi's sarcoma (KS), characterized by endothelial and spindle cell proliferation, also scattered erythrocytes and hemosiderin deposits were observed (Figure 2a, b). Human herpesvirus-8 associated antigens were detected in situ by immunohistochemistry. Serologic testing for human immunodeficiency virus was negative. Evaluation of gastrointestinal tract with endoscopy and colonoscopy showed KS lesions. Biopsy from descending colon was consistent with an involvement of KS.