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 2484  Index                                                                                            Index         2485



                  Pseudo-Zollinger-Ellison syndrome, iron   clinical features, 2269         posttransfusion, 2359, 2361
                         deficiency and, 629            complications, 2269                 vascular. See Vascular purpuras
                  PSGL-1, 1852f, 1854, 1855–1856, 1870,    definition and epidemiology, 2267  Purpura fulminans, 2104, 2207
                         1976–1977, 1977t, 1979t        differential diagnosis, 2270       PUVA (psoralen plus ultraviolet A), 433,
                  PSMD4, 1736                           etiology and pathogenesis, 2268           1686, 1687, 1689
                  Psoralen plus ultraviolet A (PUVA), 433,   in hepatic disease, 2194–2195  PV. See Polycythemia vera (PV)
                         1106, 1686, 1687, 1689         objective testing for, 2271–2273   PYD (pyridinoline), 1738
                  Psoriasis, 1575                       therapy. See Venous thrombosis/    Pyoderma gangrenosum, 2100, 2100f, 2102
                  Psychotropic drugs, 2079                   thromboembolism, therapy      Pyrazinamide, for tuberculosis, 386
                  PT. See Prothrombin time (PT)       Pulmonary eosinophilia, 949–950      Pyridinoline (PYD), 1738
                  PTCL. See Peripheral T-cell lymphoma   Pulmonary hypertension            Pyridoxine, 651, 917–918, 920
                         (PTCL)                         chronic thromboembolic, 2273       Pyrimethamine, 606t, 1269
                  PTEN, 195, 1443                       in polycythemia vera, 1293         Pyrimidine 5′-nucleotidase, 692t, 699, 700t,
                  PTEN, 231t, 1626, 1736t               in primary myelofibrosis, 1324–1325       706, 706f
                  Pteroic acid, 584                     vs. primary myelofibrosis, 1327–1328  Pyrimidine analogues, megaloblastic anemia
                  Pteroylglutamic acid (folic acid), 584, 585f.   sickle cell disease and, 769    and, 606t
                         See also Folate                treatment, 797                     Pyrimidine synthesis, 587f
                  PTGS1/COX1, 1456                    Punctate basophilia, 468             Pyrin, 298–299
                  PTLD (posttransplant lymphoproliferative   Pure erythroid leukemia, 1390  PYRIN, 1025
                         disorders), 1265–1266, 1500t, 1574,   Pure red cell aplasia       Pyropoikilocytes, 475
                         1636                           acquired, 542–545                  Pyropoikilocytosis, hereditary. See Hereditary
                  PTP (posttransfusion purpura), 2359, 2361  in chronic lymphocytic leukemia,     pyropoikilocytosis
                  PTPN11, 1346t, 1352, 1471                  1542                          Pyrrole rings, 892f
                  PTPN12, 1699                            clinical features, 543–544       Pyruvate kinase (PK)
                  PTPRD, 234t                             definition and history, 542–543   activity, 692t
                  PTPs (protein tyrosine phosphatases), 253  differential diagnosis, 544    erythrocyte aging and, 497
                  PU.1                                    etiology and pathogenesis, 543    in glucose metabolism, 696
                    in B cell function, 271               laboratory features, 544          mutants/variants, 702
                    in erythroid differentiation, 272, 483  in large granular lymphocytic leukemia,   structure, 696, 696f
                    GATA1 and, 268, 483                      1566                          Pyruvate kinase (PK) deficiency
                    in hematopoietic stem cell to common   parvovirus B19 infection and,    in animals, 704
                         lymphoid progenitor commitment,     1251–1252                      clinical features, 690, 700t
                         262                              therapy, course, and prognosis, 544–545,   diagnosis, 700t
                    in lymphopoiesis, 1155                   545f, 1542                     differential diagnosis, 691
                    in myelopoiesis, 1011               classification of, 542t             epidemiology, 690
                    RB and, 217                         inherited (Diamond-Blackfan anemia),   genetics, 702, 704
                  Pulmonary angiography, 2272                539–540, 994                   in hereditary nonspherocytic hemolytic
                  Pulmonary disease/dysfunction         during pregnancy, 120                     anemia, 709
                    in acute myelogenous leukemia, 1381  transient aplastic crisis and transient   malaria resistance and, 704
                    in adult Langerhans cell histiocytosis, 1108  erythroblastopenia of childhood,   therapy, 711–712
                    anemia and, 505                          541–542, 541f
                    in antiphospholipid syndrome, 2240  Pure white cell aplasia, 995       Q
                    in disseminated intravascular coagulation,   Purine analogues, 322–324. See also specific   22q 11.2 deletion syndrome (DiGeorge
                         2204–2205, 2205t                    drugs                                syndrome), 86–87, 1214t, 1222
                    erythrocytosis of, 872, 875, 881    adverse effects, 324               Q43P, 1838
                    in Gaucher disease, 1124            mechanism of action, 323           3q abnormalities, 1377
                    Hodgkin lymphoma treatment and lung   megaloblastic anemia and, 606t   5q-minus syndrome, 1312, 1347, 1347f
                         cancer risk, 1618              for mycosis fungoides, 1687        Quat Sha, 2107
                    after hematopoietic cell transplantation,   pharmacology, 323–324      Quebec platelet syndrome/disorder, 1853,
                         368                            structure, 323f                           1854, 2055–2056, 2138
                    in Langerhans cell histiocytosis, 1104  Purine nucleoside phosphorylase deficiency,   Quinacrine, aplastic anemia and, 515
                    primary lymphoma, 1581                   1214t, 1217                   Quinidine, 2017, 2079
                    in sickle cell disease, 768–769, 769f  Purine synthesis, 585, 586t, 587f  Quinine, 817, 819, 2015, 2017, 2245, 2262
                    in Waldenström macroglobulinemia, 1791  Purpura                        Quinolones, 384, 388–389
                  Pulmonary embolism. See also Venous   amyloid, 1774, 1774f               Quinupristin/dalfopristin, 385
                         thrombosis/thromboembolism     in immune thrombocytopenia, 2002   Quizartinib, 1403








          Kaushansky_index_p2393-2506.indd   2485                                                                       9/21/15   3:22 PM
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