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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| Format: | eBook |
| Language: | English |
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[S.l.] :
Academic Press,
2024.
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| Online Access: | ScienceDirect |
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Table of Contents:
- 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.
- 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.
- 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.
- 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.