situations, leukopenia in 60 scenarios, lymphopenia in all instances and thrombocytopenia in 80 of sufferers. Hyperferritinemia was objectified in all sufferers, hypertriglyceridemia in 4 patients and hepatic cytolysis in three sufferers. The myelogram uncovered several photographs of haemophagocytosis in 80 circumstances. The LHL was secondary to: a serious relapsing SLE in four circumstances and Still’s sickness in one situation. The treatment was the two symptomatic and etiological applying substantial dose corticosteroid therapy in all case. The evolution was favourable for all our individuals. Conclusions: Systemic disorders are amongst the aetiologies of (LHL) whose diagnosis may be tough because of the presence of various clinical and biological signs frequent to both pathologies.PB1045|International Coagulation Assays and Endothelial Biomarkers in Sufferers with Diabetes Mellitus H.Y. Lim1,two,3; B. Lui2; M. Tacey2; A. Kwok 2; S. Varadarajan2; M. Sashindranath3; C. Selan3; G. Donnan1; H. Nandurkar3; P. Ho2,University of Melbourne, Melbourne, Australia; 2Northern Health, Epping,Australia; 3Australian Centre for Blood Illnesses, Melbourne, Australia Background: Diabetes mellitus (DM) is related with enhanced threat of cardiovascular disease even though there are no present coagulation studies that predict thrombotic hazards. Aims: To investigate the utility of worldwide coagulation assays and en-PB1044|Hemophagocytic Lymphohistiocytosis Complicating Systemic Diseases I. Chabchoub1; R. Ben Salah1; F. Abida2; F. Frikha1; M. Chaari2; Z. Bahloul1dothelial biomarkers in diabetic individuals in contrast to balanced controls. Methods: Diabetic patients, not on anticoagulation and with out active malignancy, had been recruited from endocrinology outpatients. Blood samples have been collected for baseline exams and international coagulation assays including thromboelastography (TEG), CDC Inhibitor Gene ID calibrated automated thrombogram (CAT) and overall haemostatic prospective (OHP) assay as well as tissue factor pathway inhibitor (TFPI) and plasminogen activator inhibitor-1 (PA1). The results had been compared to previously recruited wholesome controls (n = 153). Effects: 184 sufferers consisting of 22 kind 1 DM (T1DM), 154 form 2 DM (T2DM) and eight latent autoimmune diabetes in adults (LADA) have been recruited. Compared to healthier controls, diabetic patients demonstrated much more hypercoagulable TEG parameters with increased clot power (maximum amplitude, 68.seven vs 60.5 mm, P 0.001). Even though there was no big difference in thrombin generation (CAT), the OHP assay demonstrated substantially increased fibrin generation and lower general fibrinolytic prospective (OFP 73.six vs 81.one , P 0.001). TFPI was significantly increased in diabetic individuals (36.9 vs 14.five ng/mL, P 0.001) whilst PAI-1 was comparable (P = 0.14). On sub-analysis, T2DM individuals have been extra hypercoagulable than T1DM sufferers on thromboelastography, and fibrin generation with greater PAI-1 (14.8 vs 8.7 ng/mL, P = 0.017) but comparable for other assays. T1DM individuals with known diabetic complications had reduce OFP than individuals with out complications although T2DM with CB2 Antagonist Accession recognized complications had higher thrombin generation parameters with lowered OFP.Internal Medication Division, Hedi Chaker Hospital, Sfax, Tunisia; Hematology Laboratory, Hedi Chaker Hospital, Sfax, TunisiaBackground: Hemophagocytic lymphohistiocytosis (HLH) is actually a rare and possibly lethal problem. It could be major or secondary and might complicate other situations: neoplastic, infectious or autoimmune. Systemic illnesses are an uncommon cause of HLH. Aims: The aim of this wor