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DIAGNOSTIC PATHOLOGY: BLOOD AND BONE MARROW

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9780323392549 ::  DIAGNOSTIC PATHOLOGY: BLOOD AND BONE MARROW
ISBN:

9780323392549

Colección:DIAGNOSTIC PATHOLOGY
EditorialELSEVIER SCIENCE PUB.B.U.
Edicion:
Páginas:950
Idioma:INGLES
P.V.P.: 227,99 € + 4% IVA = 237,11 €
Dto 5% Ahorras 11,86 €
Importe final iva incl. 225,25 €
EN PREPARACION 2018

<P>PART OF THE HIGHLY REGARDED <I>DIAGNOSTIC PATHOLOGY</I> SERIES, <B><I>DIAGNOSTIC PATHOLOGY: BLOOD AND BONE MARROW</I>, SECOND EDITION<I> </B></I>INCLUDES TODAY'S MOST RECENT KNOWLEDGE ON THE <B>LATEST FINDS IN THIS SUBSPECIALTY</B>. NEW CHAPTERS FOCUS ON<B> CURRENT MOLECULAR INSIGHTS </B>INTO THE PATHOGENESIS OF FAMILIAL DISORDERS AND NEOPLASMS, ENSURING <B>PATHOLOGISTS, HEMATOPATHOLOGISTS, HEMATOLOGISTS, </B>AND<B> ONCOLOGISTS</B> ALIKE CAN DELIVER THE MOST UP-TO-DATE DIAGNOSES POSSIBLE. CONCISE, BULLETED TEXT COUPLED WITH EXTENSIVE ILLUSTRATIONS MAKES THIS SUCCINCT YET COMPREHENSIVE REFERENCE IDEAL FOR CLINICAL USE.</P>

<P>PART I: INTRODUCTION</P> <P>HEMATOPOIESIS AND BONE MARROW HISTOLOGY</P> <P>BONE MARROW EXAMINATION AND TECHNIQUES</P> <P>BONE MARROW REPORTING</P> <P>OVERVIEW OF CONSTITUTIONAL AND ACQUIRED BONE MARROW DISORDERS</P><I> </I> <P>PART II: ANEMIA</P> <P>OVERVIEW OF ANEMIA</P><I> </I><B> <P>SECTION 1: ACQUIRED ANEMIAS</P></B> <P>IRON DEFICIENCY ANEMIA</P> <P>AUTOIMMUNE HEMOLYTIC ANEMIAS</P> <P>ALLOIMMUNE HEMOLYTIC ANEMIA AND HEMOLYTIC DISEASE OF NEWBORN</P> <P>MICROANGIOPATHIC HEMOLYTIC ANEMIA</P> <P>MEGALOBLASTIC ANEMIA</P> <P>ACQUIRED NONNEOPLASTIC SIDEROBLASTIC ANEMIA</P> <P>ALCOHOLISM-ASSOCIATED ANEMIA</P> <P>ANEMIA IN THE ELDERLY</P> <P>COPPER DEFICIENCY-ASSOCIATED ANEMIA</P> <P>ACQUIRED RED CELL APLASIA</P> <P>TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD</P> <P>PARVOVIRUS-INDUCED RED CELL APLASIA</P> <P>PAROXYSMAL NOCTURNAL HEMOGLOBINURIA</P> <P>ACQUIRED APLASTIC ANEMIA</P><B> <P>SECTION 2: CONSTITUTIONAL ANEMIAS</P></B> <P>THALASSEMIA</P> <P>SICKLE CELL ANEMIA</P> <P>PYRUVATE KINASE DEFICIENCY</P> <P>HEREDITARY SPHEROCYTOSIS</P> <P>HEREDITARY ELLIPTOCYTOSIS, INCLUDING HEREDITARY PYROPOIKILOCYTOSIS</P> <P>DIAMOND-BLACKFAN ANEMIA</P> <P>FANCONI ANEMIA</P> <P>CONGENITAL DYSERYTHROPOIETIC ANEMIA</P> <P>CONGENITAL SIDEROBLASTIC ANEMIA</P> <P>CONGENITAL MEGALOBLASTIC ANEMIA</P><I> </I> <P>PART III: ERYTHROCYTOSIS</P><B> <P>SECTION 1: CONSTITUTIONAL</P></B> <P>CONGENITAL ERYTHROCYTOSIS</P><I> </I><B> <P>SECTION 2: ACQUIRED</P></B> <P>ACQUIRED ERYTHROCYTOSIS</P> <P>PART IV: BENIGN LEUKOCYTE DISORDERS IN BLOOD AND BONE MARROW</P> <P>OVERVIEW OF BENIGN LEUKOCYTE DISORDERS IN BLOOD AND BONE MARROW</P> <P>PANCYTOPENIA</P> <P>NEUTROPENIA</P> <P>NEUTROPHILIA</P> <P>MONOCYTOSIS</P> <P>EOSINOPHILIA</P> <P>BASOPHILIA</P> <P>LYMPHOCYTOSIS</P> <P>LYMPHOPENIA, CONSTITUTIONAL AND ACQUIRED</P> <P>PLASMACYTOSIS OF BONE MARROW</P> <P>HEMATOGONES IN BONE MARROW</P> <P>LYMPHOID AGGREGATES IN BONE MARROW</P> <P>GRANULOMAS IN BONE MARROW</P> <P>PART V: CONSTITUTIONAL GRANULOCYTIC DISORDERS</P><B> <P>SECTION 1: CONSTITUTIONAL NEUTROPENIAS</P></B> <P>SEVERE CONGENITAL NEUTROPENIA AND CYCLIC NEUTROPENIA</P> <P>SHWACHMAN-DIAMOND SYNDROME</P> <P>CHEDIAK-HIGASHI SYNDROME</P> <P>MYELOKATHEXIS IN WHIM SYNDROME</P><B> <P>SECTION 2: CONSTITUTIONAL NEUTROPHIL ANOMALIES</P></B> <P>PELGER-HUET ANOMALY</P> <P>MYH9-RELATED DISORDERS</P> <P>SELECTED LYSOSOMAL STORAGE DISEASES WITH ABNORMAL LEUKOCYTE GRANULATION</P> <P>PART VI: MEGAKARYOCYTIC DISORDERS</P> <P>OVERVIEW OF MEGAKARYOCYTIC DISORDERS</P><I> </I><B> <P>SECTION 1: ACQUIRED PLATELET DISORDERS WITH THROMBOCYTOPENIA</P></B> <P>IMMUNE-MEDIATED THROMBOCYTOPENIA</P> <P>HEMOLYTIC-UREMIC SYNDROME</P> <P>THROMBOTIC THROMBOCYTOPENIC PURPURA</P> <P>PREGNANCY-ASSOCIATED THROMBOCYTOPENIA</P><B> <P>SECTION 2: CONSTITUTIONAL PLATELET DISORDERS WITH THROMBOCYTOPENIA</P></B> <P>THROMBOCYTOPENIA ABSENT RADIUS SYNDROME</P> <P>CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA</P> <P>GRAY PLATELET SYNDROME</P> <P>WISKOTT-ALDRICH SYNDROME-RELATED DISORDERS</P> <P>CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA</P><I> </I><B> <P>SECTION 3: THROMBOCYTOSIS</P></B> <P>THROMBOCYTOSIS</P> <P>PART VII: INFECTION</P> <P>OVERVIEW OF INFECTION</P> <P>HANTAVIRUS PULMONARY SYNDROME</P> <P>HUMAN IMMUNODEFICIENCY VIRUS</P> <P>INFECTIOUS MONONUCLEOSIS SYNDROMES (EPSTEIN-BARR VIRUS, CYTOMEGALOVIRUS)</P> <P>PARVOVIRUS B19 INFECTION</P> <P>BACTERIAL INFECTIONS, BLOOD AND BONE MARROW FEATURES</P> <P>FUNGAL INFECTIONS, BLOOD AND BONE MARROW FEATURES</P> <P>HELMINTHIC INFECTIONS</P> <P>MALARIA</P> <P>OTHER PROTOZOAN INFECTIONS</P> <P>PART VIII: MISCELLANEOUS NONNEOPLASTIC DISORDERS AND CONDITIONS</P> <P>OVERVIEW AND CLASSIFICATION OF HEMOPHAGOCYTIC DISORDERS IN BONE MARROW</P> <P>HEMATOLOGIC MANIFESTATIONS OF COLLAGEN VASCULAR DISORDERS</P> <P>HEMATOLOGIC MANIFESTATIONS OF CHRONIC RENAL DISORDERS</P> <P>LYSOSOMAL STORAGE DISEASES WITH PREDOMINANTLY HISTIOCYTIC STORAGE</P> <P>OTHER PREGNANCY-ASSOCIATED HEMATOLOGIC DISORDERS</P> <P>GELATINOUS TRANSFORMATION AND OTHER BONE MARROW STROMAL DISORDERS</P> <P>CRYSTALS IN BONE MARROW</P> <P>BONE ABNORMALITIES IN BONE MARROW SPECIMENS</P> <P>PART IX: MYELOID NEOPLASMS</P> <P>OVERVIEW AND CLASSIFICATION OF MYELOID NEOPLASMS</P> <P>PROTOCOL FOR THE EXAMINATION OF SPECIMENS FROM PATIENTS WITH HEMATOPOIETIC NEOPLASMS INVOLVING BONE MARROW</P> <P>CLINICAL PRACTICE GUIDELINES FOR INITIAL WORK-UP OF ACUTE LEUKEMIA</P><B> <P>SECTION 1: MYELOPROLIFERATIVE NEOPLASMS</P></B> <P>OVERVIEW OF MYELOPROLIFERATIVE NEOPLASMS</P> <P>CHRONIC MYELOGENOUS LEUKEMIA, <I>BCR/ABL1+</P></I> <P>CHRONIC NEUTROPHILIC LEUKEMIA</P> <P>POLYCYTHEMIA VERA</P> <P>PRIMARY MYELOFIBROSIS</P> <P>ESSENTIAL THROMBOCYTHEMIA</P> <P>CHRONIC EOSINOPHILIC LEUKEMIA, NOT OTHERWISE SPECIFIED</P> <P>SYSTEMIC MASTOCYTOSIS</P> <P>MAST CELL LEUKEMIA</P> <P>MYELOPROLIFERATIVE NEOPLASM, UNCLASSIFIABLE</P><B> <P>SECTION 2: MYELOID AND LYMPHOID NEOPLASMS WITH EOSINOPHILIA AND ABNORMALITIES OF PDGFRA, PDGFRB, AND FGFR1</P></B> <P>MYELOID AND LYMPHOID NEOPLASMS WITH <I>PDGFRA </I>REARRANGEMENT</P> <P>MYELOID NEOPLASMS WITH <I>PDGRFB </I>REARRANGMENTS</P> <P>MYELOID AND LYMPHOID NEOPLASMS WITH <I>FGFR1 </I>ABNORMALITIES</P><B> <P>SECTION 3: MYELODYSPLASTIC & MYELOPROLIFERATIVE NEOPLASMS</P></B> <P>OVERVIEW OF MYELODYSPLASTIC/MYELOPROLIFERATIVE NEOPLASMS</P> <P>CHRONIC MYELOMONOCYTIC LEUKEMIA</P> <P>ATYPICAL CHRONIC MYELOID LEUKEMIA, <I>BCR/ABL1-</P></I> <P>JUVENILE MYELOMONOCYTIC LEUKEMIA</P> <P>RARS-T</P> <P>MYELODYSPLASTIC/MYELOPROLIFERATIVE NEOPLASMS, UNCLASSIFIABLE</P><B> <P>SECTION 4: MYELODYSPLASTIC SYNDROMES</P></B> <P>OVERVIEW AND CLASSIFICATION OF MYELODYSPLASTIC SYNDROMES</P> <P>MYELODYSPLASIA WITH SINGLE LINEAGE DYSPLASIA</P> <P>MYELODYSPLASIA WITH RING SIDEROBLASTS</P> <P>MYELODYSPLASIA WITH MULTILINEAGE DYSPLASIA</P> <P>MYELODYSPLASIA WITH INCREASED BLASTS</P> <P>MYELODYSPLASTIC SYNDROME WITH ISOLATED DEL(5Q)</P> <P>MYELODYSPLASTIC SYNDROME, UNCLASSIFIABLE</P> <P>CHILDHOOD MYELODYSPLASTIC SYNDROME (REFRACTORY CYTOPENIA OF CHILDHOOD)</P><B> <P>SECTION 5: ACUTE MYELOID LEUKEMIA</P></B> <P>OVERVIEW OF ACUTE MYELOID LEUKEMIA</P> <P>FAMILIAL AML/MDS</P> <P>ACUTE MYELOID LEUKEMIA WITH T(8;21)(Q22;Q22), <I>RUNX1-RUNX1T1</P></I> <P>ACUTE MYELOID LEUKEMIA WITH INV(16)(P13.1Q22) OR T(16;16)(P13.1;Q22), <I>CBFB-MYH11</P></I> <P>ACUTE PROMYELOCYTIC LEUKEMIA WITH T(15;17)(Q22;Q21), <I>PML-RARA</P></I> <P>ACUTE PROMYELOCYTIC LEUKEMIA WITH VARIANT <I>RARA </I>REARRANGEMENT</P> <P>ACUTE MYELOID LEUKEMIA WITH T(9;11)(P22;Q23), <I>MLLT3-MLL</P></I> <P>ADDITIONAL GENETIC SUBTYPES OF ACUTE MYELOID LEUKEMIA, INCLUDING T(6;9), INV(3), T(1;22), MUTATED <I>NPM1</I>, MUTATED <I>CEBPA</P></I> <P>ACUTE MYELOID LEUKEMIA WITH MYELODYSPLASIA- RELATED CHANGES</P> <P>THERAPY-RELATED MYELOID NEOPLASMS</P> <P>ACUTE MYELOID LEUKEMIA WITH MINIMAL DIFFERENTIATION</P> <P>ACUTE MYELOID LEUKEMIA WITHOUT MATURATION</P> <P>ACUTE MYELOID LEUKEMIA WITH MATURATION</P> <P>ACUTE MYELOMONOCYTIC LEUKEMIA</P> <P>ACUTE MONOBLASTIC AND MONOCYTIC LEUKEMIA</P> <P>ACUTE ERYTHROID LEUKEMIA</P> <P>ACUTE MEGAKARYOBLASTIC LEUKEMIA</P> <P>ACUTE BASOPHILIC LEUKEMIA</P> <P>ACUTE PANMYELOSIS WITH MYELOFIBROSIS</P> <P>MYELOID PROLIFERATIONS RELATED TO DOWN SYNDROME</P> <P>BLASTIC PLASMACYTOID DENDRITIC CELL NEOPLASM</P> <P>PART X: ACUTE LEUKEMIAS OF AMBIGUOUS LINEAGE</P> <P>ACUTE UNDIFFERENTIATED LEUKEMIA</P> <P>MIXED PHENOTYPE ACUTE LEUKEMIA</P> <P>PART XI: LYMPHOID NEOPLASMS</P> <P>OVERVIEW OF LYMPHOID NEOPLASMS</P> <P>PROTOCOL FOR THE EXAMINATION OF SPECIMENS FROM PATIENTS WITH NON-HODGKIN LYMPHOMA/LYMPHOID NEOPLASMS</P><B> <P>SECTION 1: B-PRECURSOR NEOPLASMS</P></B> <P>B-LYMPHOBLASTIC LEUKEMIA</P> <P>NOVEL GENETIC SUBTYPES OF B-LYMPHOBLASTIC LEUKEMIA</P><B> <P>SECTION 2: T-PRECURSOR NEOPLASMS</P></B> <P>T-LYMPHOBLASTIC LEUKEMIA/LYMPHOMA</P> <P>ETP-ALL</P><B> <P>SECTION 3: MATURE B-CELL NEOPLASMS</P></B> <P>OVERVIEW AND CLASSIFICATION OF MATURE LEUKEMIAS, IMMUNOSECRETORY LYMPHOMAS</P> <P>MONOCLONAL B LYMPHOCYTES</P> <P>CHRONIC LYMPHOCYTIC LEUKEMIA/SMALL LYMPHOCYTIC LYMPHOMA</P> <P>B-CELL PROLYMPHOCYTIC LEUKEMIA</P> <P>SPLENIC B-CELL MARGINAL ZONE LYMPHOMA</P> <P>HAIRY CELL LEUKEMIA</P> <P>SPLENIC B-CELL LEUKEMIA, HAIRY CELL LEUKEMIA VARIANT</P> <P>LYMPHOPLASMACYTIC LYMPHOMA</P> <P>GAMMA HEAVY CHAIN DISEASE</P> <P>MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE</P> <P>PLASMA CELL MYELOMA</P> <P>BURKITT LEUKEMIA/LYMPHOMA</P> <P>MANTLE CELL LYMPHOMA IN BLOOD AND BONE MARROW</P> <P>FOLLICULAR CELL LYMPHOMA IN BLOOD AND BONE MARROW</P> <P>MARGINAL ZONE LYMPHOMA IN BLOOD AND BONE MARROW</P> <P>LARGE CELL LYMPHOMA IN BLOOD AND BONE MARROW</P> <P>OTHER B-CELL NON-HODGKIN LYMPHOMAS INVOLVING BLOOD AND BONE MARROW</P><B> <P>SECTION 4: MATURE T/NK-CELL NEOPLASMS</P></B> <P>OVERVIEW AND CLASSIFICATION OF MATURE T/NK-CELL NEOPLASMS</P> <P>T-CELL PROLYMPHOCYTIC LEUKEMIA</P> <P>T-CELL LARGE GRANULAR LYMPHOCYTIC LEUKEMIA</P> <P>CHRONIC LYMPHOPROLIFERATIVE DISORDER OF NK CELLS</P> <P>AGGRESSIVE NK-CELL LEUKEMIA</P> <P>ADULT T-CELL LEUKEMIA</P> <P>MYCOSIS FUNGOIDES/SÉZARY SYNDROME</P> <P>ANAPLASTIC LARGE CELL LYMPHOMA IN BLOOD AND BONE MARROW</P> <P>OTHER T-CELL NON-HODGKIN LYMPHOMAS INVOLVING BLOOD AND BONE MARROW</P><B> <P>SECTION 5: HODGKIN LYMPHOMA IN BONE MARROW</P></B> <P>HODGKIN LYMPHOMA IN BONE MARROW, CLASSIC AND LYMPHOCYTE PREDOMINANT SUBTYPES</P> <P>PROTOCOL FOR THE EXAMINATION OF SPECIMENS FROM PATIENTS WITH HODGKIN LYMPHOMA</P> <P>PART XII: OTHER NEOPLASMS INVOLVING BONE MARROW</P> <P>LANGERHANS CELL HISTIOCYTOSIS IN BONE MARROW</P> <P>HEMOPHAGOCYTIC DISORDERS</P> <P>POSTTRANSPLANT LYMPHOPROLIFERATIVE DISORDERS IN BONE MARROW</P> <P>METASTATIC CARCINOMA AND SARCOMA</P>

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