The Stokes-Einstein (SE) relation is examined for hard-sphere (HS) and Weeks-Chandler-Andersen (WCA) fluids by the molecular dynamics method on temperatures and densities corresponding to the saturated vapor line of Lennard-Jones (LJ) liquids. While the self-diffusion coefficient, D, and shear viscosity, ηsv, increases and decreases, respectively, with increasing steepness in interaction potentials, the same SE relation holds for HS and WCA fluids as that obtained for LJ liquids, i.e., Dηsv = (kBT/C)(N/V)1/3, where kB is the Boltzmann constant, T is the temperature, and N is the particle number included in the system volume V. The coefficient C is almost constant at about 6 to 2π for η > 0.3, where η is the packing fraction. The results show that the SE relation for simple liquids and fluids does not need to bear any concepts of both the hydrodynamic particle size and the boundary condition. In light of this SE relation, the Enskog, Eyring-Ree, and Zwanzig theories are quantitatively tested. In addition, the cause of deviation from unity of the exponent in the fractional SE relation for simple fluids is clearly accounted for. The present results show that applying both the original and the fractional SE relations to simple liquids and fluids does not lead to any meaningful discussions.

Secondary non-Hodgkin lymphoma following acute myeloid leukemia (AML) is extremely rare. We here describe a unique case involving a patient who developed Epstein-Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL) during complete remission (CR) of AML. A 75-year-old Japanese man was initially diagnosed with AML with maturation (FAB M2), bearing chromosomal translocation t(3,4)(p25;q21). After intensive chemotherapy, bone marrow aspiration revealed normal karyotype, and he achieved CR. Six years and 4 months later, he was still in CR from AML, but developed DLBCL presenting in the terminal ileum. Cytogenetic analysis of the DLBCL cells showed the same translocation as the previous AML. The rearrangements of the immunoglobulin heavy chain genes of the two malignancies were examined using polymerase chain reaction amplification, and the rearrangement patterns were found to differ from each other. Our data thus suggest that, in the present case, the AML and DLBCL arose from a common progenitor cell, as indicated by the clonal abnormality t(3,4)(p25;q21), and that different immunoglobulin heavy chain gene rearrangements occurred during each course of clonal evolution.

Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA)-related disease that manifests as a triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury (AKI) and is caused by uncontrolled activation of the complement system. We report the case of a 61-year-old woman with acute type A aortic dissection that subsequently developed into aHUS. The hematologic disorders underlying aHUS improved after treatment with the complement inhibitor eculizumab. It is important to consider aHUS when a patient clinically develops a triad of microangiopathic hemolytic anemia, thrombocytopenia, and an increasing creatinine level following cardiovascular surgery.

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