Hematology

• Pyruvate Kinase Deficiency
• Abilirubinuria jaundice syndrome
• Acute hemorrhagic anemia
• Zygomycosis
• Paget's disease-like reticulocytosis
• Erythropoietic porphyria
• Eosinophilia
• Eosinophilic leukemia
• Haemophilus influenzae skin infection
• Post-transfusion thrombocytopenic purpura
• Pine caterpillar osteoarthritis
• Leukopenia and agranulocytosis
• Leukemia
• Leukemic angina
• Bleeding disorders
• Pure red cell aplastic anemia
• Hypocalcemia and hypomagnesemia
• Thalassemia
• Multiple myeloma
• Malignant histiocytosis
• Malignant lymphoma
• Bone marrow tuberculosis anemia
• Myelofibrosis
• Myelodysplastic syndrome
• Allergic purpura
• Acquired platelet dysfunction
• Acquired Circulatory Anticoagulant Hypertension Syndrome
• Hodgkin lymphoma
• Macroglobulinemia
• Acute leukemia
• Megaloblastic anemia
• Acute lymphoblastic leukemia
• Lymphopenia
• Sickle cell disease
• Leukemia reaction
• Agranulocytosis
• Green tumor
• Anemia of chronic disease
• Disseminated intravascular coagulation
• Chronic myelogenous leukemia
• Chronic lymphocytic leukemia
• Congestive splenomegaly
• Anemia
• Hypersplenism
• Glucose-6-phosphate dehydrogenase deficiency
• Iron deficiency anemia
• Anemia due to excessive hemolysis
• Hemolytic anemia
• Eosinophilia
• Idiopathic hypereosinophilic syndrome
• Idiopathic thrombocytopenic purpura
• Iron utilization anemia
• Vitamin K deficiency
• Thrombotic thrombocytopenic purpura
• Thrombocytopenia
• Hemophilia
• Congenital erythrocytic disease
• Von Willebrand disease
• Hereditary hemochromatosis
• Anemia due to folic acid deficiency
• Hereditary hemorrhagic telangiectasia
• Nutritional megaloblastic anemia
• Idiopathic thrombocytopenic purpura
• Essential thrombocythemia
• Abnormal hemoglobinopathies
• Neutropenia
• Aplastic anemia
• Autoimmune hemolytic anemia
• Polycythemia vera
• Paroxysmal nocturnal hemoglobinuria
• Anemia due to acute blood loss
• Disseminated intravascular coagulation
• Congenital pure red cell aplastic anemia
• Congenital dyserythropoietic anemia
• Myelo-pancreatic syndrome
• Alloimmune neonatal thrombocytopenic purpura
• Mycobacterium intracellularis infection
• Infectious lymphocytosis
• Geomycosis
• Giant platelet disease
• Arteriosclerosis obliterans
• Giant cell arteritis scleritis
• Acute myeloid leukemia
• Chronic lymphocytic leukemia
• Leukocyte Glucose-6-Phosphate Dehydrogenase Deficiency
• Traumatic cardiogenic hemolytic anemia
• Adult T-cell leukemia
• Hyperimmunoglobulin E syndrome
• Secondary leukemia
• Reactive histiocytosis
• Rheumatic anemia
• Acquired circulating anticoagulant hyperplasia
• Gitlin syndrome
• Acute agranulocytosis
• Acute lymphoblastic leukemia
• Plasma cell leukemia
• Mycobacterium kansasii infection
• Mycobacterium ulcerans infection
• Sickle cell anemia
• Blastomyces dermatitidis
• Light chain disease and light chain deposition disease
• Penicillosis
• Hemolytic anemia caused by arsine
• Congenital leukemia
• Relative polycythemia
• Hereditary hemorrhagic telangiectasia
• Transient hypogammaglobulinemia in infancy
• Neutropenia
• Histiocytic necrotizing lymphadenitis
• Pseudomonas aeruginosa infection
• Infectious thrombocytopenic purpura
• Sulfhaemoglobinemia
• Angioimmunoblastic lymphadenopathy
• Thrombosis
• Alpha-reservoir disease
• Hodgkin's disease
• Nizhnov syndrome
• Anemia due to liver disease
• Pyrimidine 5'-nucleotide deficiency
• Allergic purpura nephritis
• Acquired hemophilia
• Westcott-Aldrich syndrome
• Hereditary protein C deficiency
• Serum sickness and serum sickness-like reactions
• Primary cutaneous B-cell lymphoma
• Protoporphyria
• Hypoproliferative acute leukemia
• Toxic purpura
• Penicillosis marneffei
• Sepsis and Bacteremia
• Senile purpura
• Congenital atransferrinemia
• Langerhans histiocytosis
• Pure red blood cell aplasia
• Methotrexate-Associated Lymphoproliferative Disorders
• Pediatric acute lymphoblastic leukemia
• Congenital nonhemolytic jaundice
• Hairy cell leukemia
• Acute intermittent porphyria
• Warm antibody autoimmune hemolytic anemia
• Hemolytic anemia caused by hyperthermia
• Paroxysmal cold hemoglobinuria
• Anemia of chronic disease
• Geriatric acute leukemia
• Purpura fulminans
• Hemolytic anemia due to lead poisoning
• Secondary sideroblastic anemia
• Lymphoma cell leukemia
• Basophilic leukemia
• Mental disorders associated with leukemia
• Mental disorders associated with anemia
• Hemolytic uremic syndrome
• Thrombocytopenia
• Hemophilia A
• Folic acid deficiency
• Chronic hematogenous osteomyelitis
• Anemia due to hypothyroidism
• Chronic myeloid leukemia
• Wound botulism
• Leukemia kidney damage
• Disseminated intravascular coagulation
• Unstable hemoglobinopathies
• C5 insufficiency syndrome
• Castleman disease
• Adult chronic myeloid leukemia
• Pasteurella haemorrhagic infection
• Skin manifestations of DF-2 sepsis
• Delta-reservoir disease
• Large granular lymphocytic leukemia
• Monocytic leukemia
• Reactive plasmacytosis
• Acute nonlymphocytic leukemia in the elderly
• Acute lymphoblastic leukemia in the elderly
• Skin leukemia
• Subcutaneous panniculitis inflammatory T-cell lymphoma
• Amyloidosis
• Sinus histiocytosis with giant lymphadenopathy
• Mast cell leukemia
• Pulmonary eosinophilic infiltrates
• Glucose phosphoisomerase deficiency
• Bacillary epithelioid angiomatosis
• Heparin-induced thrombocytopenia
• Anemia due to infectious disease
• High altitude polycythemia
• Myelopathic anemia
• Mycobacterium chelae infection
• Cavernous hemangioma thrombocytopenia syndrome
• Erythropoietic protoporphyria
• Anti-activated protein C disease
• Necrotizing sarcoid-like granulomatosis
• Mixed porphyria
• Acquired vitamin K-dependent coagulation factor abnormalities
• Acute eosinophilic pneumonia
• Acute myeloid leukemia
• Acute heterozygous leukemia
• Acute promyelocytic leukemia
• Hexokinase deficiency
• Secondary monoclonal immunoglobulin disease
• Secondary myelofibrosis
• Secondary polycythemia
• Secondary cutaneous follicular center cell lymphoma
• Secondary thrombocytosis
• Acanthocytosis secondary to severe liver disease
• Familial polycythemia
• Capsular histoplasmosis
• Progressive pigmented purpuric dermatosis
• Stomatocytosis
• Lazy leukocyte syndrome
• Histiocytosis of Langhans cells
• Leukopenia and agranulocytosis in the elderly
• Sepsis in the elderly
• Disseminated intravascular coagulation in the elderly
• Hypocalcemia in the elderly
• Multiple Myeloma in the Elderly
• Myelodysplastic syndrome in the elderly
• Allergic purpura in the elderly
• Hodgkin lymphoma in the elderly
• Megaloblastic anemia in the elderly
• Anemia of chronic disease in the elderly
• Chronic myeloid leukemia in the elderly
• Chronic lymphocytic leukemia in the elderly
• Immune thrombocytopenic purpura in the elderly
• Iron deficiency anemia in the elderly
• Hemolytic anemia in the elderly
• Thrombotic disease in the elderly
• Primary myelofibrosis in the elderly
• Essential thrombocythemia in the elderly
• Aplastic anemia in the elderly
• Polycythemia vera in the elderly
• Cold antibody autoimmune hemolytic anemia
• Cold agglutinin syndrome
• Cryoglobulinemia kidney damage
• Fusarium disease
• Sickle cell nephropathy
• Mycobacterium scrofula infection
• Chronic alcoholism
• Chronic renal anemia
• Trichosporidiosis
• Mucormycosis
• Rh incompatibility hemolytic disease
• Telangiectatic annular purpura
• Melanie's Gangrene
• Meningococcal bacteremia
• Skin lymphogranulomatosis
• Granulomatous loose skin
• Sezeri syndrome
• Sarcoidosis of the nervous system
• Basophilia
• Pediatric leukemia
• Acquired coagulation factor abnormalities due to severe liver disease
• Myelomonocytic leukemia
• Myeloperoxidase deficiency
• Idiopathic delayed immunoglobulin deficiency
• Idiopathic eosinophilic syndrome
• Hemolytic anemia due to copper poisoning
• Painful cyanosis syndrome
• Microangiopathic hemolytic anemia
• Centipede sting
• Congenital agamma-globulinemia
• Congenital aplastic anemia
• Microscopic polyangiitis
• Pediatric alpha-thalassemia
• Pediatric beta thalassemia
• Pediatric Echo and Coxsackie Virus Infection
• Pediatric adult chronic myeloid leukemia
• Neonatal hemorrhage
• Neonatal purpura
• Marching hemoglobinuria
• Hemoglobin C disease
• Hemoglobin D disease
• Hemoglobin E disease
• Hemoglobin M disease
• Abnormal platelet procoagulant activity
• Thrombocytopenic purpura
• Platelet-type pseudovonoid hemophilia
• Hemophilia B
• Mycosis fungoides and Sezary syndrome
• Drug immune thrombocytopenic purpura
• Drug-related immune hemolytic anemia
• Post-transplant lymphoproliferative disease
• Inherited protein S deficiency
• Hereditary coproporphyria
• Hereditary methemoglobinemia
• Hereditary antithrombin III deficiency
• Hereditary prothrombin deficiency
• Hereditary factor V deficiency
• Hereditary factor VII deficiency
• Hereditary factor XIII deficiency
• Hereditary factor X deficiency
• Hereditary factor XI deficiency
• Hereditary spherocytosis
• Hereditary sideroblastic anemia
• Hereditary Elliptocytosis
• Hereditary fibrinogen deficiency
• Hereditary dysfibrinogenemia
• Abnormal gamma-globulinemia
• Prolymphocytic leukemia
• Juvenile myelomonocytic leukemia
• Juvenile chronic myeloid leukemia
• Stasis purpura
• Lymphoproliferative disorders associated with primary immune disorders
• Primary monoclonal immunoglobulin disease
• Primary hyperlipoproteinemia and xanthoma hyperplasia
• Primary myelofibrosis
• Primary mixed cryoglobulinemic vasculitis
• Primary macroglobulinemia
• Primary macroglobulinemia renal impairment
• Primary cutaneous immunocytoma
• Primary fibrinolysis
• Toxic methemoglobinemia
• Central nervous system leukemia
• Neutropenia
• Heavy chain disease
• Thalassemia
• Autoerythrocyte hypersensitivity purpura
• Broad bean disease
• Chronic myelomonocytic leukemia
• Blood poison
• Blood stasis constitution
• Congenital leukocyte dysgranulosis syndrome
• Old rotten legs
• Hypocalcemia
• Leukopenia
• Nutritional anemia
• Blood disease
• Congenital factor X deficiency
• Hemolytic jaundice
• Thick blood
• Microcytic hypochromic anemia
• Acute myeloid leukemia