Page 2511 - Williams Hematology ( PDFDrive )
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2482           Index                                                                                                                                                                                               Index         2483




               Pregnancy, 119–126                     postpartum hemorrhage and, 1987, 2137,   heart, 1581
                 acute fatty liver of, 2012, 2211          2138                           paranasal sinuses, 1581
                 acute intermittent porphyria and, 901  preeclampsia in, 2011–2012, 2210–2211  skin, 1581
                 acute myelogenous leukemia during, 1409  Rh blood groups and, 2336       spleen, 1582
                 adaptations to, 119                  sepsis during, 2211               Primary mediastinal large B-cell lymphoma,
                 alloimmunized, 849, 853f. See also   sickle cell disease and, 772–773         1634–1635
                       Alloimmune hemolytic disease of   thalassemia syndromes in, 126    clinical features, 1634
                       the fetus and newborn (HDFN)   thrombocytopenia during, 121–122,   definition, 1634
                 anemia in, 120                            2010–2012, 2010t               epidemiology, 1634
                 anticoagulant therapy during, 112, 112t,   thrombophilia in, 122–123, 2221, 2225t,   gene mutations, 225t, 1496t, 1597f, 1626
                       2277                                2227                           laboratory features, 1496t, 1596, 1596f,
                 antiphospholipid syndrome in, 2239, 2244,   thrombophilia testing in, 2228t, 2229  1634
                       2245                           thrombotic microangiopathy in, 2262  therapy, 1635
                 aplastic anemia and, 518             toxoplasmosis in, 1269            Primary myelofibrosis (PMF), 1319–1332
                 blood volume, erythropoietin level, and   von Willebrand disease and, 121, 2176  clinical features, 1324–1325
                       hemoglobin concentration in, 119  warfarin therapy during, 112, 112t  bone changes, 1325, 1325t
                 carbon monoxide poisoning in, 796  Pregnane X receptor, 893                extramedullary tumors, 1324
                 chemotherapy during, 124           Prekallikrein (PK), 1929, 2121          immune and inflammatory, 1325
                 chronic myelogenous leukemia during,   Preleukemic anemia, 1342            portal hypertension and varices and
                       1459–1460                    Preleukemic stem cells, 1376               pulmonary arterial hypertension,
                 coagulation factor deficiencies and, 121,   Prenatal diagnosis/testing        1324–1325
                       2135, 2141, 2144               for hemophilia A, 2116                prefibrotic stage, 1323t, 1324
                 cobalamin deficiency in, 598         for hemophilia B, 2127                presenting signs, 1324
                 congenital thrombotic thrombocytopenic   for thalassemias, 754             presenting symptoms, 1324
                       purpura in, 2257–2258          for von Willebrand disease, 2174      thrombocytosis, 1311
                 disseminated intravascular coagulation   Prepromultimerin, 1845            thrombosis and bleeding, 2079–2081
                       during, 120–121, 2204t,      Presenilin, 1013                        thrombosis and hemorrhage, 1325
                       2210–2211                    Preventive hematology, 7              course and prognosis, 1278, 1331–1332
                 essential thrombocythemia and, 124–125,   Priapism, 770                  definition and history, 1319
                       1314–1315, 2081              Primary adrenal lymphoma, 1583        differential diagnosis, 1311, 1327–1328,
                 factor V deficiency in, 2138       Primary autoimmune myelofibrosis, 1327     1449–1450
                 fibrinogen abnormalities in, 2155, 2156,   Primary central nervous system lymphoma,   epidemiology, 1319–1320
                       2159                                1244f, 1246, 1579              essential thrombocythemia and, 1312–
                 fibrinolytic activity during, 2312  Primary cutaneous anaplastic large cell   1313
                 folate requirements/deficiency in, 120, 584,   lymphoma, 1499t, 1687, 1688,   etiology and pathogenesis, 1320–1323
                       597–598, 599                        1688f                            CD34+ cell egress and neoplastic
                 HELLP syndrome in. See HELLP       Primary cutaneous diffuse large B-cell     megakaryocytopoiesis, 1321
                       syndrome                            lymphoma, leg type, 1637         chromosomal abnormalities, 178, 179t
                 hematologic consultation in, 45–46  Primary cutaneous follicular center    clonal myeloid disease, animal models,
                 hematologic malignancies in, treatment of,   lymphoma (PCFCL), 184t, 1581     and activating mutations, 1320–
                       123–124                      Primary cutaneous marginal zone B-cell     1321
                 hemoglobinopathies in, 125–126            lymphoma (PCMZL), 184t, 1581     enhanced angiogenesis and splenic
                 heparin-induced thrombocytopenia in,   Primary cutaneous peripheral T-cell    endothelial cells, 1321
                       2032                                lymphomas, 1499t                 exogenous factors, 1320
                 hereditary spherocytosis and, 674  Primary effusion lymphoma, 1246–1247,   extramedullary hematopoiesis, 1278,
                 HIV infection in, 1269                    1496t                               1323
                 hypertension during, neonatal neutropenia   Primary extranodal lymphoma, 1579–1583  fibroplasia, 1322–1323, 1322t
                       and, 994                       bone, 1583                            gene mutations, 228–229t, 1278, 1308t,
                 inherited platelet disorders in, 2062  breast, 1583                           1320–1321
                 iron deficiency in, 120, 630         central nervous system, 1244f, 1246, 1579  hematopoietic dysfunction, 1321–1322
                 lymphoma treatment during, 1634      chest and lung, 1581                  immune mechanisms, 1320
                 mononucleosis in, 1269               endocrine glands, 1583              laboratory features, 1325–1327
                 paroxysmal nocturnal hemoglobinuria   eye, 1574, 1579–1581                 blood cell counts and morphology,
                       and, 580                       gastrointestinal tract, 1581             1323f, 1323t, 1325–1326
                 parvovirus B19 infection in, 849     genitourinary, 1246, 1581–1582, 1582f,   functional abnormalities of blood cells,
                 polycythemia vera in, 125, 2081           1634                                1326








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