Page 2525 - Williams Hematology ( PDFDrive )
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2496           Index                                                                                                                                                                                               Index         2497




               Thalassemias, 725–754                  clinical use, 334                   generation, 1918–1919, 1919f, 1940, 1940f,
                 clinical features, 743–745, 744f, 744t  for Langerhans cell histiocytosis, 1106,   1949, 1950f
                 definitions and history, 725              1107                           in inflammatory response, 1979t, 2201
                 differential diagnosis, 568–569, 748, 749f  for malignant histiocytic diseases, 1110  inhibitors, 1919, 1919t
                 epidemiology and population genetics,   for mantle cell lymphoma, 1659t, 1660t  PI3K pathway and, 1841
                       727–728, 727f                  mechanism of action, 334            in platelet activation, 2293
                 etiology and pathogenesis, 728–730, 729f  for myelodysplastic syndromes, 1359  platelet activation and, 1834, 1836, 1845,
                 forms, 726, 726t                     for myeloma, 1750, 1752, 1752t, 1754     1919
                   α. See α-thalassemias              pharmacology, 334                   structure, 1919
                   β. See β-thalassemias              for primary myelofibrosis, 1329     in thrombosis and hemostasis, 1979t
                   δ, 726, 736, 751                   structure, 333f                     transforming growth factor β and, 1848
                   δβ. See δβ-thalassemias          THBD, 1931–1932, 1932f              Thrombin-activatable fibrinolysis inhibitor
                   εγδβ, 735, 745, 751              T-helper cells. See CD4+ T cells           (TAFI), 1972
                   εωδβ, 726                               (helper T cells)               activation, 1935
                   hereditary persistence of fetal   T-helper type 1 (Th1) cells, 1180, 1181f  aging and, 135
                       hemoglobin and. See Hereditary   T-helper type 2 (Th2) cells, 1180, 1181f  characteristics, 1916t, 1935, 2308
                       persistence of fetal hemoglobin   T-helper type 9 (Th9) cells, 1181f, 1182  in disseminated intravascular coagulation,
                       (HPFH)                       T-helper type 17 (Th17) cells, 1182, 2000  2206
                 as global health problem, 754      Theophylline, cAMP inhibition and, 404  in fibrinolysis, 2203
                 globin gene clusters and, 728–730, 729f  Therapeutic apheresis. See Apheresis  gene structure and variations, 1935–1936
                 hemoglobin C, 749–750              Therapy-related myeloid neoplasms     plasminogen and, 2154
                 hemoglobin E, 750                    acute myelogenous leukemia. See Acute   structure, 1935, 2308
                 hyposplenism and, 868                     myelogenous (myeloid) leukemia   Thrombin-antithrombin (TAT) complexes,
                 i antigen and, 2340                       (AML), therapy-related              2209
                 intermedia, 725, 753                 myelodysplastic syndromes. See    Thrombin receptor antagonists, 406,
                 laboratory features, 745–748, 746f, 747f  Myelodysplastic syndrome (MDSs),    2076–2077
                 major, 725                                therapy-related              Thrombin time, 1989
                 minima, 725                        Thiamine deficiency, 652            Thromboatherogenesis, 1092
                 minor, 553, 636, 725               Thiamine-responsive megaloblastic anemia,   Thrombocythemia, BCR-ABL-positive, 1449
                 molecular basis, 730–739. See also specific   608, 652                 Thrombocytopenia, 1993–2018
                       forms                        Thiazides, maternal ingestion of, effect on   acquired pure amegakaryocytic, 1999
                 pathophysiology, 739–743                  fetus and newborn, 112, 112t   in acute myelogenous leukemia, 1381
                   abnormal iron metabolism, 742    Thienopyridines, 2074t, 2075–2076     alcohol consumption and, 1998
                   cellular heterogeneity, 741      6-Thioguanine                         in alloimmune hemolytic disease of the
                   clinical heterogeneity, 742–743, 743f  for acute lymphoblastic leukemia, 1505,   fetus and newborn, 849
                   coagulation defects, 742                1516, 1517                     in antiphospholipid syndrome, 2240
                   compensatory mechanisms for anemia,   for acute myelogenous leukemia, 1395t,   classification, 1994t
                       741                                 1399, 1409                     consultative approach to, 42–43
                   erythroid precursor damage, 740–741  adverse effects, 324              cyclic, 2015
                   imbalance globin-chain synthesis, 740  for autoimmune hemolytic anemia,    definition and history, 1993–1994
                   infection, 742                          839                            diagnosis, 1740, 1994
                   persistent fetal hemoglobin production,   mechanism of action, 323     drug-induced, 2015–2018, 2016t, 2017t,
                       741                            megaloblastic anemia and, 606t           2077
                   red cell damage, 740–741           pharmacology, 323–324               etiology and pathogenesis, 1985, 1986t
                   splenomegaly, 742                  structure, 323f                     gestational, 45, 121–122, 2010
                 pregnancy and, 126                 Thiopurine methyltransferase, 316, 319t, 323,   heparin-induced. See Heparin-induced
                 prevention of, 753–754                    1516                                thrombocytopenia (HIT)
                 prognosis, 753                     6-Thiopurines, 319t, 323              in hepatic disease, 2194
                 sickle cell, 749                   Thiotepa, 331, 331t, 332t             in Hodgkin lymphoma, 1610
                 treatment, 362–363, 751–753, 2372  Thomsen-Friedenreich (T) antigen, 2262  hypersplenism and, 2014
               Thalassic anemia, 725                Thorium dioxide, 518                  hypothermia and, 2014
               Thalidomide, 333–335                 Thrombin, 290, 1877                   immune. See Immune thrombocytopenia
                 for acute myelogenous leukemia, 1404  binding to fibrinogen and fibrin, 2154  (ITP)
                 for adult Langerhans cell histiocytosis,   in disseminated intravascular coagulation,   in inherited platelet disorders, 1996–1997,
                       1109                                2200–2201                           1998t. See also Platelets, disorders
                 adverse effects, 334, 1741, 1757     formation, 1842, 1854               interferon-induced, 1825








          Kaushansky_index_p2393-2506.indd   2496                                                                       9/21/15   3:23 PM
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