Hematology-Oncology


Acute Granulocytic Febrile Transfusion Reaction
Acute Hemolytic Transfusion Reaction
Acute Intermittent Porphyria
Acute Lymphocytic Leukemia (ALL)
Acute Myeloid Leukemia (AML, Acute Myelogenous Leukemia)
Adenoid Cystic Carcinoma
Afibrinogenemia
Amyloidosis
Anemia
Anemia of Chronic Disease
Anti-Factor VIII Antibody
Anti-Fibrinolytics
Anti-Phospholipid Antibody Syndrome
Antithrombin Deficiency
Aplastic Anemia
Asplenia
Autoimmune Lymphoproliferative Syndrome (Canale-Smith Syndrome)
Babesiosis
Bernard-Soulier Syndrome
Blood Products
Bone Marrow Biopsy
Carcinoid Tumor
Chondrosarcoma
Chronic Eosinophilic Leukemia
Chronic Granulomatous Disease (CGD)
Chronic Lymphocytic Leukemia (CLL)
Chronic Myeloid Leukemia (CML, Chronic Myelogenous Leukemia)
Chronic Myeloproliferative Diseases
Chronic Neutrophilic Leukemia
Coagulopathy
Cold Agglutinin Disease
Complement-Mediated Hemolytic-Uremic Syndrome (Complement-Mediated HUS)
Complete Blood Count (CBC)
Cryoprecipitate
Delayed Hemolytic Transfusion Reaction
Disseminated Intravascular Coagulation (DIC)
Drug-Induced Thrombotic Microangiopathy
Dysfibrinogenemia
Elevated Plasma D-Dimer
Elevated Serum Lactate Dehydrogenase (LDH)
Engraftment Syndrome
Essential Thrombocythemia (Esssential Thrombocytosis)
Evan’s Syndrome
Ewing Sarcoma
Exchange Transfusion
Extramedullary Hematopoiesis
Extranodal NK/T-Cell Lymphoma, Nasal Type (ENKL)
Fabry Disease
Factor V Deficiency
Factor V Leiden
Factor VII Deficiency
Factor VIII + Von Willebrand Factor Complex (Humate-P)
Factor IX Complex (Prothrombin Complex Concentrate)
Factor IX Concentrate
Factor X Deficiency
Factor XI Deficiency
Factor XII Deficiency
Factor XIII Deficiency
Felty Syndrome
Fluorodeoxyglucose Positron Emission Tomography (FDG-PET)
Fresh Frozen Plasma (FFP)
Gaucher Disease
Graft vs Host Disease (GVHD)
Glanzmann’s Thrombasthenia
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD Deficiency)
Hairy Cell Leukemia
Head and Neck Cancer
HELLP Syndrome
Hematopoietic Stem Cell Transplant (HSCT) (Bone Marrow Transplant, BMT)
Hemochromatosis
Hemolytic Anemia
Hemolytic-Thrombocytopenic Syndromes
Hemophagocytic Syndrome
Hemophilia A
Hemophilia B
Heparin-Induced Thrombocytopenia (HIT)
Hereditary Elliptocytosis
Hereditary Hemorrhagic Telangiectasia (HHT) (Osler-Weber-Rendu Syndrome)
Hereditary Spherocytosis
Hereditary Stomatocytosis
High Molecular Weight Kininogen Deficiency
Histiocytic Disorders
Hodgkin’s Disease
Hypercoagulable States
Hypereosinophilic Syndrome
Hyperfibrinolytic States
Hyperproteinemia
Hyperviscosity
Hypofibrinogenemia
Immune Defects
Immune Reconstitution Syndrome
Immune Thrombocytopenic Purpura (ITP)
Iron Deficiency Anemia
Iron Overload
Iron Studies
Kaposi Sarcoma
Kasabach-Merritt Syndrome (Giant Hemangioma)
Leiomyosarcoma
Leukopenia
Liposarcoma
Leukostasis
Lymphadenopathy
Lymphoma
Lymphomatoid Granulomatosis
Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer, HNPCC)
Macrophage Activation Syndrome (MAS)
Langerhans Cell Histiocytosis (LCH)
Methemoglobinemia
Methylenetetrahydrofolate Reductase (MTHFR) Gene Mutation
Multiple Myeloma
Mycosis Fungoides
Myelodysplastic Syndrome
Myelofibrosis-Myelophthisis
Neuroblastoma
Neurofibromatosis
Neutropenia
NK Cell Leukemia (aka Aggressive NK Cell Leukemia, ANKL)
Osteosarcoma
Packed Red Blood Cells (PRBC)
Pancytopenia
Paraproteinemia
Paroxysmal Cold Hemoglobinuria
Paroxysmal Nocturnal Hemoglobinuria (PNH) (Marchiafava–Micheli Syndrome)
Peripheral Eosinophilia
Peripheral Blood Smear
Pernicious Anemia
Plasmacytoma
Plasmapheresis
Plasminogen Activator Inhibitor-1 (PAI-1) Deficiency
Platelet Inhibition
Platelet Transfusion
Polycythemia
Polycythemia Vera
Post-Transfusion Purpura
Prekallikrein Deficiency
Primary Myelofibrosis
Protein C Deficiency
Protein S Deficiency
Prothrombin Complex Concentrate (Factor IX Complex)
Prothrombin Deficiency (Factor II Deficiency)
Prothrombin G20210A Gene Mutation
Pure Red Cell Aplasia
Purpura
Radiation Therapy
Rh Incompatibility
Rhabdomyosarcoma
Sezary Syndrome
Shiga Toxin-Producing Escherichia Coli Hemolytic-Uremic Syndrome (Shiga Toxin-Producing Escherichia Coli HUS)
Sickle Cell Disease
Sideroblastic Anemia
Splenic Infarction
Splenic Rupture
Splenomegaly
Splenosis
Sulfhemoglobinemia
Systemic Mastocytosis
Teratoma
Thalassemias
Thrombocytopenia
Thrombocytosis
Thromboelastography (TEG)
Thrombolytics
Thrombotic Thrombocytopenic Purpura-Acquired (Acquired TTP)
Thrombotic Thrombocytopenic Purpura-Hereditary (Hereditary TTP)
Thrombotic Microangiopathy
Thymic Mass
Transfusion-Associated Graft vs Host Disease
Trousseau’s Syndrome (Migratory Superficial Thrombophlebitis)
Tumor Lysis Syndrome
Tumor Markers
Von Willebrand Disease
Waldenstrom’s Macroglobulinemia
Wilm’s Tumor