A 47-year-old man presented with a febrile ulceronecrotic dermatosis. He reported intense use of levamisole-contaminated cocaine during the previous weeks.Physical examination revealed a high fever (40°C) combined with diffuse necrotic papulopustules involving 90% of the body surface ( Fig. 1a,b). The patient's condition rapidly worsened with severe respiratory distress. Biological investigation revealed elevated C-reactive protein (60 mg/L, normal range 0-5 mg/ L) normocytic anaemia (haemoglobin 9.5 g/dL; normal range 13.0-18.0 g/dL) and hepatic cytolysis (transaminases and alkaline phosphatase three times the normal value, and gamma-glutamyltransferase 2fold above the normal value). Tests for infectious disease (blood tests for varicella zoster virus, herpes simplex virus, human immunodeficiency virus, hepatitis B and C viruses, human herpes virus(HHV)-6 and HHV-8, syphilis, Epstein-Barr virus, cytomegalovirus, Pneumococcus, Mycoplasma pneumoniae, bacterial and mycological cutaneous samples and blood cultures) were negative, as were screening tests for autoimmunity.Thoracic computed tomography scan showed ground-glass opacities in the upper lobes combined with perihilar cylindrical bronchodilation.Histopathology of a skin biopsy revealed a diffuse dermoepidermal lymphocyte and neutrophil infiltrate. Leucocytoclastic vasculitis was associated with necrosis of the blood vessel walls and extravasation of erythrocytes (Fig. 2).Based on the clinicopathological findings, febrile ulceronecrotic Mucha-Habermann disease (FUMHD) was suggested.Systemic steroids 1 mg/kg/day were promptly administered, but the patient's condition deteriorated with severe dyspnoea and extension of the cutaneous lesions. Chest radiography confirmed a worsened interstitial pneumonia, leading to an emergency orotracheal intubation. Intravenous immunoglobulin (IVIG) 2 g/kg (IVIG) resulted in a favourable respiratory and cutaneous response in a few days. IVIG was continued twice a month for a year, producing improvement in skin lesions (Fig. 1c) and liver function tests. After 22 months of follow-up, only hyperpigmented scars (Fig. 1d) were noted. Since then, the patient has completely stopped his cocaine use.FUMHD is considered as a rare and severe variant of pytiriasis lichenoid and varioliformis acuta (PLEVA), with a potentially life-threatening prognosis due to severe systemic visceral involvement. The pathogenesis of FUMHD is unclear. A complex immune vasculitis related to a hypersensitivity reaction towards an infectious antigen has been suspected. 1 The infiltration of CD8 lymphocytes around the epidermis and dermis, suggesting a cytotoxic attack of lymphocytes to altered epidermal antigens, could be an argument in favour of an immunological process. 2 Levamisole is an imidazothiazole drug often used as an adulterant in drugs to produce a better stimulant effect and to increase the drug weight. It has immunostimulant properties, which may result in a leucocytoclastic vasculitis. Levamisole has been reported to cause severe cutaneous vascul...