Hematology case review is a comprehensive text that covers the expansive knowledge about the study of blood cells. After collecting blood smears and bone marrow aspirates for over 40 years, Dr. Doll has created the most up to date and comprehensive compilation of hematology case studies. These samples form the core of the case studies featured in this book, including benign disorders, such as hereditary spherocytosis, to neoplastic neoplasms like acute leukemia. Within the text, both rare and common conditions are discussed, with the presenting symptoms, blood counts, and pertinent images. The book is formatted in an interactive problem-based layout in order to enhance the question and answer features of the book.

Chronic lymphocytic leukemia with prolymphocytic transformation -- Microcytic anemia secondary to iron deficiency -- Acute myeloid leukemia with t(8;21) -- Macrocytic anemia secondary to folate deficiency -- Chronic myeloid leukemia -- Hereditary spherocytosis -- Acute promyelocytic leukemia -- Cold agglutinin disease -- Acute monocytic leukemia -- Alpha thalassemia trait -- Blue toe syndrome secondary to essential thrombocytosis -- Thrombotic thrombocytopenic purpura associated with HIV infection -- Primary myelofibrosis -- Acute lymphoblastic leukemia FAB L2 type -- Spur cell anemia -- Hairy cell anemia -- Polycythemia vera -- Burkitt leukemia/acute lymphoblastic leukemia FAB L3 type -- Refractory anemia with ring sideroblasts -- Chronic myelomonocytic leukemia -- Waldenstrom's macroglobulinemia -- Hyposplenism secondary to sickle cell anemia -- Chronic lymphocytic leukemia with Richter's transformation -- Acute erythroid leukemia -- Systemic mastocytosis -- Disseminated histoplasmosis associated with HIV infection -- Disseminated mycobacterium avium infection associated with HIV infection -- Myelodysplastic syndrome with 5q deletion -- Autoimmune hemolytic anemia -- Aplastic anemia -- Follicular lymphoma in leukemic phase -- Hemoglobin CC disease -- Hemoglobin E-beta-null thalassemia -- Myelophthisic anemia presenting with leukoerythroblastosis -- Splenic marginal zone lymphoma in leukemic phase -- Chronic neutrophilic leukemia -- Chronic eosinophilic leukemia -- Congenital dyserythropietic anemia -- T-cell prolymphocytic leukemia -- B-cell prolymphocytic leukemia -- Refractory cytopenia with unilineage dysplasia -- Refractory anemia with ring sideroblasts with thrombocytosis -- Chronic lymphocytic leukemia with associated autoimmune hemolytic anemia -- Cold agglutinin disease secondary to EBV infection -- Evans syndrome -- Macrophage activation syndrome -- Gelatinous transformation of bone marrow associated with anorexia nervosa -- Pyruvate kinase deficiency -- Hemolytic anemia secondary to spider bite -- Malaria -- Plasma cell leukemia -- Amegakaryocytic thrombocytopenia -- Hairy cell leukemia variant -- Acute promyelocytic leukemia microgranular variant -- Mixed-lineage acute leukemia -- Therapy-related acute myeloid leukemia -- Acute myeloid leukemia -- Sideroblastic anemia -- Chediak Higashi syndrome -- Chronic myelomonocytic leukemia type 2 -- Diffuse large B-cell lymphoma in leukemic phase -- Acute myelomonocytic leukemia -- Paroxysmal Nocturnal hemoglobinuria -- Multiple myeloma -- Immune thrombocytopenia -- Sicke-beta(+) thalassemia -- Sulfhemoglobinemia -- T-cell large granular lymphocyte leukemia -- Mantle cell lymphoma in leukemic phase -- Ehrlichiosis -- Pure red cell aplasia -- Bernard Soulier syndrome -- Hemoglobin SC disease -- Cocaine-associated neutropenia -- Sarcoidosis-associated neutropenia -- May Hegglin anomaly -- Post-splenectomy-associated monocytosis -- Chronic myelomonocytic leukemia with eosinophilia -- Acute myeloid leukemia with inv (16) -- Hypersplenism-induced pancytopenia -- Polyclonal lymphocytosis -- Natural killer cell leukemia -- Diamond Blackfan anemia -- Fanconi anemia -- Hepatitis C-associated immune thrombocytopenia -- Loiasis -- Beta thalassemia trait -- Pseudothrombocytopenia secondary to platelet satellitism -- Hereditary elliptocytosis -- Hemolytic uremic syndrome -- Acute megakaryoblastic leukemia associated with mediastinal germ cell tumor -- Sezary syndrome -- Thrombotic thrombocytopenic purpura -- Familial Pelger Huet anomaly -- T-cell acute lymphoblastic leukemia.