Sir, Purpura fulminans (PF) is usually associated with meningococcemia or invasive pneumococcal infection. Here, we report a case of PF due to imported Plasmodium falciparum malaria in an asplenic patient. A 51-year-old Caucasian man was admitted to the Emergency Department because of fever and confusion. He had just returned 13 days earlier after a long stay in Madagascar. He had a history of posttraumatic splenectomy in his childhood. He had no antimalarial chemoprophylaxis. He had fever and asthenia 4 days before the admission, and took one dose of dirithromycin orally. Once in the Emergency Department, he was confused, his blood pressure was 100/ 60 mmHg, and his temperature 38.7 C. A peripheral blood smear revealed erythrocytes infected by P. falciparum. A treatment with intravenous quinine was initiated without loading dose. The patient was transferred to the ICU where he presented generalized tonic–clonic seizure and coma, leading to intubation for mechanical ventilation and sedation with midazolam and fentanyl. At this point, he was severely shocked (blood pressure 60/40 mmHg) and anuric. A physical examination showed cold extremities and extensive necrotic and purpuric skin lesions on his hands and legs. There was no focal neurological deficit or neck stiffness. All peripheral pulses were palpable. The rest of the examination showed no abnormalities. Parasitemia was 12%. Arterial blood gas measurements showed: pH 7.21; pCO2 31 mmHg; bicarbonate level 12 mmol/L and PaO2/FiO2 ratio 315. Laboratory studies revealed the following values: blood urea nitrogen 24 mmol/L; serum creatinine 437 lmol/L; lactates 6.5 mmol/L; serum bilirubin166 lmol/L; normal glycemia. Other laboratory test results are displayed in Table 1. He received intravenous fluid, norepinephrin, low dose hydrocortisone, intravenous quinine, ceftriaxone after blood cultures, and renal replacement by continuous venovenous hemofiltration (ultrafiltration rate at 33 mL/kg per h). CT scan of the brain showed a subarachnoid hemorrhage. An electroencephalogram revealed no ongoing seizure activity. Vitamin K and platelets transfusion were given for 3 days, and fibrinogen and antithrombin concentrates on day 5. All blood cultures remained negative. The purpura progressed to skin necrosis of the two forefeet. The patient’s condition improved progressively, but his two forefeet were amputated 2 months later and the patient was discharged to a rehabilitation unit. Secondary hematological explorations revealed no deficiency of protein C, protein S, and antithrombin. The most likely diagnosis was falciparum malaria complicated by disseminated intravascular