Page 2519 - Williams Hematology ( PDFDrive )
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2490           Index                                                                                                                                                                                               Index         2491




               Scramblase, 662                      Serotonin transporter (SERT), 1879  SHMT (serine hydroxymethyltransferase),
               Scurvy (vitamin C deficiency), 652, 1986,   Serpentine receptors. See G-protein–coupled   584–585
                       2108, 2108f                         receptors (GPCRs)            Shock, in disseminated intravascular
               SCYA3, 1632                          SERPIN, 1958                               coagulation, 2204, 2205t
               SDF-1. See CXCL12 (stromal cell-derived   SERPINA1, 1699                 Short tandem repeats (STRs), 147
                       factor-1)                    SERPINA10, 1938                     Shoulder pain, history of, 6
               Sea-blue histiocytes, 1446           SERPINC1, 1937                      SHP1 (hematopoietic cell phosphatase), 253,
               Sealing zones, 60                    Serpins (serine protease inhibitors), 1145,   485, 486f, 1163
               Sec1/Munc18 (SM), 1849                      1958, 2304t, 2307–2308       Shwachman-Diamond syndrome, 532,
               SEC23B, 564, 567                     Serratia marcescens, 106, 1030, 1033       993–994, 1026
               Seckel syndrome, 530t, 532           SERT (serotonin transporter), 1879  Sialoadhesin (Siglec1), 1054, 1080, 1081f,
               Secondary myelofibrosis, 1325        Serum sickness, 2103, 2103f                1082, 1083f
               Secretory protein, 1161              SETBP1, 1348, 1472                  Sialomucins, 67t, 68
               Secretory vesicles, 930t, 1009       Severe combined immunodeficiency (SCID),   Sialophorin, 1873
                                                                                                 0
               Sedormid purpura, 824                       1216–1219                    Sickle cell β -thalassemia, 762
               Segmented granulocytes, 32t, 34        adenosine deaminase deficiency, 439  Sickle cell β+-thalassemia, 762
               Segmented neutrophils, 32t             clinical features, 1214t, 1218    Sickle cell disease, 762–776
               Selectins (lectins), 66, 67t. See also E-selectin;   cytokine-mediated signaling defects and,   clinical features and management,
                       L-selectin; P-selectin              249, 1217–1218                      766–773, 767t
                 counterreceptors, 282t               defective signaling through T-cell receptor   in anesthesia and surgery, 773
                 expression, 281                           and, 1218                        aplastic crises, 767
                 functions, 1054                      definition and history, 1216–1217     avascular necrosis, 771, 771f
                 ligands, 1057t                       gene mutations, 1154, 1575t           cardiac, 769
                 structure, 282t                      increased lymphocyte precursor apoptosis   dactylitis, 771
               Selenium, 652t                              in, 1217                         hepatobiliary, 772
               Selenium deficiency, 654               laboratory features, 1214t, 1218      hyperhemolytic crises, 767
               Self-antigens, 2343                    lymphomas and, 1575t                  infection, 773
               Self-inactivating (SIN) viral vectors, 437  molecular defects and pathogenesis, 1217,   leg ulcers, 771–772
               Senicapoc, for sickle cell disease, 777t    1217f                            nocturnal enuresis, 770–771
               Senile purpura, 2107, 2108f            neutropenia in, 993                   ophthalmic, 772
               Sepsis                                 therapy, course, and prognosis,       osteomyelitis, septic arthritis, and bone
                 activated protein C and, 1956             1218–1219                           infarction, 771
                 C. perfringens, 819                   gene therapy, 437, 439, 453, 1219    osteopenia and osteoporosis, 771
                 disseminated intravascular coagulation   hematopoietic cell transplantation, 363,   pain control, 767–768
                       and, 2202, 2207                     1219                             in pregnancy, 772–773
                 hyposplenism and, 868                X-linked, 437, 439                    priapism, 770
                 postsplenectomy, 2004              Severe-deviation clonal myeloid disorders,   pulmonary, 768–769, 769f
                 during pregnancy, 2211                    1276t, 1279–1280                 renal failure, 770
                 transfusion-related, 2376          Sexual history, 7                       sequestration crises, 767
                 tumor necrosis factor -α in, 285   Sézary cell, 1683f, 1684f               splenic, 772
               SEPT10, 1643                         Sézary syndrome (SS), 1498t, 1679, 1683t,   stroke, 769–770
               Septic arthritis, 771                       1684t. See also Cutaneous T-cell   vasoocclusive crises, 766–767, 768f
               Sequestration crisis, in sickle cell disease, 767  lymphoma (CTCL); Mycosis   course and prognosis, 766
               Serglycin, 1011                             fungoides (MF)                 epidemiology, 763
               Serial analysis by recombinant expression   SF1, 1348                      G6PD deficiency and, 690
                       cloning (SEREX), 421         SF3B1, 227t, 231t, 1346t, 1349, 1529  history, 762–763, 762f
               Serial analysis of gene expression (SAGE),   SFA1. See CD151               hyposplenism and, 868
                       421                          SGI-110, for myelodysplastic syndromes,   i antigen and, 2340
               Serine hydroxymethyltransferase (SHMT),     1361                           inheritance, 149, 149f
                       584–585                      SH2B3 (LNK), 229t, 232t, 233t         laboratory features, 762f, 766, 779f
               Serine proteases, 1012t, 1013, 1916–1917,   Shiga toxin E. coli-associated hemolytic   modifiers of disease severity, 773–774
                       1918t                               uremic syndrome (STEC-HUS),    pathophysiology, 763–766, 764f, 765f
               Serosal implants, for primary myelofibrosis,   2255, 2258–2259               abnormal cell adhesiveness, 764–765
                       1330                         Shigella dysenteriae, 2340              activation of coagulation system, 765
               Serotonin (5-hydroxytryptamine), 286t, 289,   Shigella flexneri, 1066f       adenosine signaling, 765–766
                       1848, 1878–1879              SHIP1, 1443                             cellular dehydration, 764








          Kaushansky_index_p2393-2506.indd   2490                                                                       9/21/15   3:22 PM
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