Page 2509 - Williams Hematology ( PDFDrive )
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2480           Index                                                                                                                                                                                               Index         2481




               Plerixafor, 355                      Polycythemia (erythrocytosis), 506–510,   testosterone treatment-related, 872, 879,
               Plethora, 8                                 871–884. See also Polycythemia      880f
               Plg. See Plasminogen (Plg)                  vera                             tumors and, 872, 879, 881
               PLL. See Prolymphocytic (prolymphoblastic)   apparent (relative), 872, 880  spurious, 872, 884
                       leukemia (PLL)                 classification, 509–510, 509t, 871–872  stress, 872
               Pluripotential stem cell lesion, 1439–1440  clinical features, 506, 508–509, 880–881  therapy, 884
               Pluripotential stem cell pool, 1283    consultative approach to, 44–45   Polycythemia hypertonica, 872
               PLZF, 230                              course and prognosis, 884         Polycythemia vera (PV), 1291–1301
               PLZF, 1405                             definition and history, 871–872     clinical features, 1293–1295
               PMA (phorbol myristate acetate), 1011  differential diagnosis, 882–884, 883f  leukemic transformation, 178, 1295
               PMF. See Primary myelofibrosis (PMF)   epidemiology, 872–873                 signs and symptoms, 1293–1294, 1294f
               PML (progressive multifocal            etiology and pathogenesis, 873–880    spent phase, 1294–1295, 1294f
                       leukoencephalopathy), 1536     laboratory features, 505f, 881–882    thrombosis and bleeding, 2079–2081
               PML (promyelocytic leukemia). See Acute   neonatal, 879–880, 881             thrombosis and hemorrhage, 1286,
                       promyelocytic leukemia (APL)   pathophysiology, 506, 508f               1293
               PML-RARα                               primary familial and congenital, 509, 509t,   transition to other clonal myeloid
                 in acute myelogenous leukemia, 1377,      871                                 diseases, 1280, 1295
                       1384t                           Chuvash polycythemia. See Chuvash   course and prognosis, 1278t, 1301, 1301f
                 in acute promyelocytic leukemia, 181, 225,   polycythemia                definition and history, 1291
                       230, 240, 1390–1392, 1415       clinical features, 880             differential diagnosis, 1297, 1297t,
               PMN (polymorphonuclear neutrophils), 940f  definition and history, 871          1449–1450
               Pneumococcal polysaccharide vaccine     disorders of hypoxia sensing. See   epidemiology, 1291
                       (PPV23), 773                        Hypoxia sensing, disorders of  etiology and pathogenesis, 1278,
               Pneumococcal vaccine (PCV7), 773        epidemiology, 872                       1291–1292
               Pneumococcus infections, 384. See also   etiology and pathogenesis, 873, 873t,   chromosomal abnormalities, 178, 179t
                       Bacterial infections                874f, 877–878                    gene mutations
               Pneumocystis jiroveci (P. carinii) infections  laboratory features, 881        frequency, 1308f
                 cytomegalovirus infection and, 1268   pheochromocytoma and, 879, 881         JAK2, 228t, 1278, 1308f
                 in HIV infection, 1239, 1240, 1241t   VHL mutations associated with, 510,    JAK2 V617F , 178, 1292, 1295–1296,
                 in hyperimmunoglobulin M syndromes,       876–877, 877f, 878f, 882t           1312f, 1313f
                       1213                           renal, 879–880. See also Renal          TET2, 229t, 1292, 1308f
                 idiopathic CD4+ T lymphocytopenia and,    transplantation, erythrocytosis   iron deficiency and, 629
                       1206                                following                      laboratory features, 1295–1296
                 in immunocompromised host, 384       secondary, 509, 509t, 871–872         blood findings, 1295
                 prevention, 389, 524, 1115, 1241t, 1514  chemically induced tissue hypoxia and,   clonality in female subjects, 1296
                 in severe combined immunodeficiency       876                              erythroid colony cultures, 1296
                       syndrome, 1218                  course and prognosis, 884            erythropoietin levels, 883, 1296
                 treatment, 386                        definition and history, 871–872      JAK2 exon 12 mutations, 1296
               PNH. See Paroxysmal nocturnal           in Eisenmenger syndrome, 872, 876,    JAK2 V617F  mutations, 1295–1296
                       hemoglobinuria (PNH)                881                              marrow findings, 1296
               Pocked (pitted) red cells, 468          endocrine disorders and, 872, 879, 880f  in pregnancy, 125, 2081
               Podoplanin, 1870–1871                   epidemiology, 872–873              surgical considerations, 1294
               Podosomes, 60                           erythrocyte enzyme deficiencies and,   treatment, 1297–1301, 1298t
               POEMS syndrome (osteosclerotic myeloma),    876                              erythrocytapheresis, 429t, 432
                       9, 1733, 1746                   etiology and pathogenesis, 874       JAK inhibitors, 341–342
               Poikilocytosis, 21, 21f                 high altitude. See High-altitude     plethoric phase, 1297–1300
               Poloxamer 188, for sickle cell disease,     polycythemia                       anagrelide, 1300
                       777t                            high oxygen-affinity hemoglobins and,   aspirin, 1300, 2081
               Polyamines, 200                             782, 872, 876                      epigenetic modulation, 1300
               Polyarteritis nodosa, 2106, 2106f       laboratory features, 882               interferon, 1299
               Polychromatophilic cells, 21            post–renal transplant. See Renal       JAK2 inhibitors, 1300
               Polychromatophilic erythroblasts, 34, 463f,   transplantation, erythrocytosis   myelosuppression, 1298–1299
                       464–465, 465f                       following                          phlebotomy, 1299–1300
               Polychromatophilic erythrocytes, 34     pulmonary disease and, 872, 881        summary, 1300
               Polychromatophilic megaloblasts, 595f   sleep apnea-related, 872, 876          symptomatic therapy for pruritus,
               Polyclonal hematopoiesis, 83.1012       smoking-related, 872, 876, 876t         1300








          Kaushansky_index_p2393-2506.indd   2480                                                                       9/21/15   3:22 PM
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