Atlas of hematopathology with 100 case studies /

This comprehensive medical atlas, authored by Faramarz Naeim and colleagues, provides an in-depth exploration of hematological structures and conditions. It features 100 case studies detailing disorders of the bone marrow, white and red blood cells, and platelets. The book covers a wide array of top...

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Glavni avtor: Naeim, Faramarz
Drugi avtorji: Rao, P. Nagesh, Song, Sophie X.
Format: eKnjiga
Jezik:angleščina
Izdano: [S.l.] : Academic Press, 2024.
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Online dostop:ScienceDirect
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100 1 |a Naeim, Faramarz. 
245 1 0 |a Atlas of hematopathology with 100 case studies /  |c Faramarz Naeim, P. Nagesh Rao, Sophie X. Song. 
260 |a [S.l.] :  |b Academic Press,  |c 2024. 
300 |a 1 online resource 
505 0 |a Front Cover -- Atlas of Hematopathology with 100 Case Studies -- Atlas of Hematopathology with 100 Case Studies -- Copyright -- Contents -- Preface -- Acknowledgment -- 1 -- Hematology associated structures -- Bone marrow -- Bone marrow sample preparation -- Hematopoietic components in normal bone marrow -- Myeloid series -- Granulocytic lineage -- Mast cells -- Monocytic lineage -- Dendritic cells -- Erythroid lineage -- Megakaryocytic lineage -- Lymphocytic lineage -- Other bone marrow cells -- Blood -- Red blood cells -- White blood cells -- Platelets -- Lymph nodes -- Follicular structures -- The paracortex -- The medulla -- Spleen -- White pulp -- Marginal zone -- Red pulp -- Extramedullar hematopoiesis -- Additional resources -- 2 -- Disorders of bone marrow structure and function -- Hypocellular bone marrows -- Inherited bone marrow failure syndromes -- Fanconi anemia -- Morphology -- Genetics -- Dyskeratosis congenita -- Morphology -- Genetics -- Shwachman-Diamond syndrome -- Morphology/laboratory findings -- Genetics -- Diamond-Blackfan anemia -- Morphology and laboratory findings -- Genetics -- Amegakaryocytosis -- Morphology and laboratory findings -- Genetics -- Acquired aplastic anemia -- Morphology and laboratory findings -- Genetics -- Paroxysmal nocturnal hemoglobinuria -- Morphology and laboratory findings -- Flow cytometry -- Genetics -- Gelatinous transformation of bone marrow -- Post chemotherapy and radiation changes -- Bone marrow changes post stem cell transplantation -- Differential diagnosis -- Hypercellular bone marrows -- Reactive granulocytic hyperplasia -- Reactive erythroid hyperplasia -- Granulomas-reactive histiocytic hyperplasia -- Bone marrow metastasis -- Other bone marrow lesions -- Bone marrow necrosis -- Amyloidosis -- Bone marrow fibrosis -- Additional resources. 
505 8 |a 3 -- Disorders of white blood cells and platelets -- Qualitative abnormalities in the granulocytic series -- Toxic granulation -- Dohle inclusion bodies -- May-Hegglin anomaly -- Alder-Reilly anomaly -- Chediak-Higashi syndrome -- Pelger-Huet anomaly -- Hypersegmented and dysplastic neutrophils -- Quantitative abnormalities in the granulocytic series -- Neutrophilia -- Eosinophilia -- Basophilia -- Neutropenia -- Monocytosis and monocytopenia -- Monocytosis -- Monocytopenia -- Lymphocytosis and lymphocytopenia -- Lymphocytosis -- Infectious mononucleosis -- Morphology and laboratory findings -- Laboratory findings -- Genetics -- Differential diagnosis -- Persistent polyclonal B-cell lymphocytosis -- Lymphocytopenia -- Quantitative abnormalities in platelets -- Thrombocytosis -- Thrombocytopenia -- Autoimmune thrombocytopenic purpura -- Morphology and laboratory findings -- Differential diagnosis -- Drug-induced immune thrombocytopenia -- Posttransfusion purpura -- Thrombotic thrombocytopenic purpura/hemolytic uremic syndrome -- Morphology and laboratory findings -- Differential diagnosis -- Qualitative disorders of platelets -- Bernard-Soulier syndrome -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Glanzmann thrombasthenia -- Morphology and immunophenotype -- Molecular and cytogenetic features -- Differential diagnosis -- Wiskott-Aldrich syndrome -- Dense granule deficiency -- Alpha-granule deficiency -- Acquired platelet disorders -- Drug-induced platelet disorders -- Aspirin -- Beta-lactam antibiotics -- Additional resources -- 4 -- Disorders of red blood cells -- Abnormal morphology -- Congenital dyserythropoietic anemias -- CDA type I -- CDA type II -- CDA type III -- CDA group IV -- CDA group V -- CDA group VI -- Morphology and laboratory findings -- Macrocytic anemias -- Megaloblastic anemias -- Folate deficiency. 
505 8 |a Histiocytic disorders -- Gaucher disease -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Nieman-Pick disease -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Chediak-Higashi syndrome -- Histiocytic proliferations -- Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy -- Erdheim-Chester disease -- Juvenile xanthogranuloma -- ALK-positive histiocytosis -- Hemophagocytic lymphohistiocytosis -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Histiocytic sarcoma -- Dendritic cell disorders -- Langerhans cell histiocytosis -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Langerhans cell sarcoma -- Mature plasmacytoid dendritic cell proliferation (MPDCP) associated with myeloid neoplasm -- Blastic plasmacytoid dendritic cell neoplasm -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Interdigitating dendritic cell tumor -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Additional resources -- 7 -- Myeloproliferative neoplasms -- Chronic myeloid leukemia -- Morphologic and laboratory findings -- Chronic phase -- Blast phase -- Immunophenotyping -- Flow cytometry -- Immunohistochemical stains -- Genetics -- Differential diagnosis -- Polycythemia vera -- Morphology and laboratory findings -- Polycythemic phase -- Spent phase and postpolycythemic myelofibrosis -- Immunophenotype -- Genetics -- Primary myelofibrosis -- Morphology and laboratory findings -- Prefibrotic/early stage -- Overt fibrotic stage -- Genetics -- Essential thrombocythemia -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Chronic neutrophilic leukemia -- Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Chronic eosinophilic leukemia. 
505 8 |a Morphology and laboratory findings -- Genetics -- Differential diagnosis -- Juvenile myelomonocytic leukemia -- Morphology and laboratory findings -- Immunophenotype and cytochemical stains -- Flow cytometry (Fig. 7.31) -- Immunohistochemistry and cytochemical stains -- Genetics -- MPN, not otherwise specified -- Additional resources -- 8 -- Mastocytosis -- Classification -- Cutaneous mastocytosis -- Systemic mastocytosis -- Mast cell sarcoma -- Pathology -- Morphology and laboratory findings -- Immunophenotypic studies -- Genetics -- Differential diagnosis -- Disorders with similar clinical manifestation but lack of histologic evidence of cutaneous or systemic mastocytosis -- Disorders associated with increased mast cells or elevated serum tryptase -- Additional resources -- 9 -- Myelodysplastic neoplasms and myelodysplastic/myeloproliferative neoplasms -- Myelodysplastic neoplasms -- Classification -- MDS with defining genetic abnormalities, and MDS, morphologically defined -- Morphology -- Dysplastic erythropoiesis -- Dysplastic myelopoiesis -- Dysplastic megakaryocytes and platelets -- Immunophenotypic studies -- Flow cytometry -- Blast enumeration -- Detection of immunophenotypic aberrancies and dysmaturation patterns -- Immunohistochemical studies -- Genetics -- Cytogenetics -- Molecular genetics -- Other types of MDS -- Therapy-related MDS -- Childhood MDS -- MDS with fibrosis -- Nonclonal myelodysplasia -- Autoimmune myelodysplasia -- HIV-associated myelodysplasia -- Paraneoplastic myelodysplasia -- Myelodysplasia associated with heavy metal intoxication or deficiency -- Myelodysplasia associated with chemotherapy, irradiation, or medication -- Differential diagnosis -- Myelodysplastic/myeloproliferative neoplasms -- Chronic myelomonocytic leukemia -- Morphology and laboratory findings -- Immunophenotype and cytochemical stains. 
520 |a This comprehensive medical atlas, authored by Faramarz Naeim and colleagues, provides an in-depth exploration of hematological structures and conditions. It features 100 case studies detailing disorders of the bone marrow, white and red blood cells, and platelets. The book covers a wide array of topics, including inherited bone marrow failure syndromes, various types of anemia, leukemias, and histiocytic disorders. It serves as a crucial resource for medical professionals, particularly those specializing in pathology and laboratory medicine, offering insights into diagnostic processes and morphological findings. The atlas aims to enhance understanding and improve diagnostic accuracy in hematopathology.  |7 Generated by AI 
650 0 |a Hematology  |v Atlases. 
650 6 |a Hématologie  |0 (CaQQLa)201-0005704  |v Atlas.  |0 (CaQQLa)201-0378089 
650 7 |a Hematology  |2 fast  |0 (OCoLC)fst00954904 
655 7 |a Scientific atlases  |2 fast  |0 (OCoLC)fst01941304 
700 1 |a Rao, P. Nagesh. 
700 1 |a Song, Sophie X. 
776 0 8 |i Print version:  |z 0443188386  |z 9780443188381  |w (OCoLC)1406407781 
856 4 0 |3 ScienceDirect  |u https://www.sciencedirect.com/science/book/9780443188381