Page 2457 - Williams Hematology ( PDFDrive )
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2428           Index                                                                                                                                                                                               Index         2429




               Erythrocyte antigens (Cont.):          automated analysis, 13–16             functions of, 104–105
                 diseases associated with, 2340, 2341–2342t,   collection by apheresis, 2368  life span, 104
                       2342–2343                      composition, 469                    nucleated, 47–48
                 enzymes/chemicals affecting, 2339     carbohydrates, organic acids, and   organelle removal in, 478
                 expression, 104, 2336–2337, 2340          metabolites, 471t              pocked (pitted), 468
                 genetics, 2339                        coenzyme and vitamins, 470t        in polycythemia vera, 1295
                 immunogenicity, 2336                  electrolytes, 471t                 precursor cell kinetics, 75t
                 protein, 2337                         nucleotides, 470t                  precursors, 463–465, 463f, 464f, 465f
                 serologic detection, 2348–2350, 2349t,   phospholipids, 469t             production. See Erythropoiesis
                       2350t                           protein and water content, 469t    progenitors, 463
               Erythrocyte binding-like antigen, 815  concentration of, in clonal hematopoietic   splenic clearance/sequestration, 90–91
               Erythrocyte enzyme disorders, 689–712.      disorders, 1284–1285           viscosity, 668
                       See also specific enzymes      deformability, 469–471, 499       Erythrocyte zinc protoporphyrin, 635
                 clinical features, 708–710, 876      destroyed, fate of, 499–500, 500f  Erythrocytosis. See Polycythemia
                 course and prognosis, 712            destruction/turnover, 495–500. See also   (erythrocytosis)
                 definition and history, 689–690           Hemolysis                    Erythroderma, history of, 6
                 differential diagnosis, 711           in anemia of inflammation, 550   Erythroid cells
                 epidemiology, 690, 690f               in situ localization of, 496–498, 497f  heme synthesis in, 895–896
                 etiology and pathogenesis, 691–699, 876  measurement of, 495–496, 496f   marrow, 34
                 genetics, 699–708                     mechanisms of, 498–499, 619      Erythroid colony cultures
                 laboratory features, 710–711          senescence and, 497–498            in polycythemia diagnosis, 882
                 therapy, 711–712                     disorders                           in polycythemia vera, 1296
               Erythrocyte membrane, 661–669, 662f     anemia. See Anemia               Erythroid Kruppel-like factor (EKLF), 484
                 altered surface properties, 499       from chemical or physical agents,   Erythroid/megakaryopoietic progenitors, 271
                 damage to, 809                            809–811                      Erythroid progenitors, 271, 463
                 deformability, 668                    enzyme. See Erythrocyte enzyme   Erythroleukemia, 1390
                 ion transport and exchange channels, 668,   disorders                  Erythromelalgia, 1293, 1294f, 1308, 2080
                       669f                            fragmentation. See Hemolytic anemia,   Erythron, 461. See also Erythrocytes
                 lipids, 662                               fragmentation                Erythrophagocytosis, 619, 1050f
                 in newborn, 104–105                   membrane. See Erythrocyte membrane   Erythropoiesis, 508f
                 organization, 667–668                     disorders                      androgens and, 560
                 permeability, 669, 669f               paroxysmal nocturnal hemoglobinuria.   anemia and, 505–506
                 proteins. See Membrane proteins           See Paroxysmal nocturnal       in anemia of inflammation, 551–552
                 stability, 668                            hemoglobinuria (PNH)           effective, 489–490
               Erythrocyte membrane disorders, 21f     polycythemia (erythrocytosis). See   embryonic and fetal, 480
                 acanthocytosis, 680–681                   Polycythemia                   erythroblast enucleation in, 481–482
                 cryohydrocytosis, 682t, 684          fetal, antigen development on, 2337–2338  ferrokinetics, 490–491, 490f, 491t
                 familial deficiency of high-density   hemoglobin and, 479–480            hepcidin regulation by, 622
                       lipoproteins, 684              inclusions, 467–468, 468f           history of, 479
                 hereditary elliptocytosis. See Hereditary   iron deficiency and, 633, 633f, 634f  ineffective, 490
                       elliptocytosis (HE)            life span, 495                        as cause of iron overload, 641
                 hereditary pyropoikilocytosis. See   marrow, 34                          lead and, 811
                       Hereditary pyropoikilocytosis (HPP)  mass measurement, 488–489, 882, 1295  measurements, 489–491
                 hereditary spherocytosis. See Hereditary   membrane. See Erythrocyte membrane  megaloblastic anemia and, 597
                       spherocytosis (HS)             metabolism, 691–699                 microRNAs in, 487–488
                 laboratory features, 670f, 671f       antioxidant enzymes, 698–699       neonatal, 102–105
                 neuroacanthocytosis. See              glucose                            phylogeny, 479–480
                       Neuroacanthocytosis               enzymes, 692t, 694–697           precursor cells in, 481, 482f, 482t, 483f
                 protein defects, 670t                   pathways, 692–694, 693f          progenitor cells in, 32.2–3, 480f
                 Rh-deficiency syndrome, 684           glutathione, 698                   regulation, 482–487, 504f
                 Southeast Asian ovalocytosis, 680     nucleotide, 699                      deterministic model of lineage
                 stomatocytosis. See Stomatocytosis   morphology, 21, 21                       commitment, 483, 483f
               Erythrocytes                            in marrow infiltration, 658, 659f    erythropoietin in, 484
                 aged, 134, 471, 473, 497–498          pathophysiology of, 472–473t, 473, 475  erythropoietin receptor in, 484–485, 486f
                 antibodies. See Erythrocyte antibodies  structure and shape, 468–469, 468f  hypoxia-inducible factors in, 486–487,
                 antigens. See Erythrocyte antigens   neonatal, 102–105, 103t                  486f








          Kaushansky_index_p2393-2506.indd   2428                                                                       9/21/15   3:21 PM
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