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Hematology - Blood Disorder Buzzwords - Statistics

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General Stats
  • This quiz has been taken 16 times
    11 since last reset
  • The average score is 19 of 91
Answer Stats
Condition Symptoms Answer % Correct
leukemia auer rods AML
60%
leukemia philadelphia chromosome CML
60%
thrombocytopenia ADAMSTS1 antibody TTP
60%
leukemia MC childhood malignancy ALL
40%
leukemia overproliferation of mature lymphocytes CLL
40%
leukemia 9-22 chromosomal translocation CML
40%
anemia fava beans, dapsone, primaquine G6PD deficiency
40%
anemia HFE protein mutation hemochromatosis
40%
anemia bronze skin, DM, cardiomyopathy, hypogonadism, erectile dysfunction hemochromatosis
40%
hemophilia hemarthrosis hemophilia
40%
hemophilia factor 8 deficiency hemophilia A
40%
hemophilia factor 9 deficiency hemophilia B
40%
lymphoma painful LAD after alcohol consumption Hodgkins lymphoma
40%
lymphoma associated w/ EBV Hodgkins lymphoma
40%
myeloma preleukemic disorder that may progress to AML myelodysplasia
40%
anemia autoimmune destruction of intrinsic-factor producing parietal cells pernicious anemia
40%
anemia vasocclusive crisis sickle cell anemia
40%
thrombocytopenia post-viral infection TTP
40%
thrombocytopenia isolated PLT defect TTP
40%
anemia hypersegmented neutrophils, macroovalocytes (2) vitamin B12 and B9 deficiency
40%
leukemia hypercellular bone marrow w/ > 20% blasts ALL
20%
anemia thalassemia MC in east asians alpha thalassemia
20%
anemia heinz bodies (2) alpha thalassemia, G6PD deficiency
20%
anemia increased hepcidin and ferritin, decreased serum iron and TIBC anemia of chronic disease
20%
anemia thalassemia MC in meditteraneans beta thalassemia
20%
lymphoma mandibular/maxillary mass burkitt's lymphoma
20%
lymphoma EBV endemic to South Africa burkitt's lymphoma
20%
lymphoma starry sky appearance on histology burkitt's lymphoma
20%
lymphoma aggressive subtype of nonhodkins lymphoma burkitt's lymphoma
20%
leukemia leukemia cutis CLL
20%
leukemia smudge cells CLL
20%
leukemia treated w/ tyrosine kinase inhibitors CML
20%
thrombocytopenia elevated d-dimer DIC
20%
anemia absorbed in jejunum folic acid deficiency
20%
anemia episodic hemolytic anemia G6PD deficiency
20%
anemia jaundice G6PD deficiency
20%
anemia x-linked disorder (3) G6PD deficiency, hemophilia A, hemophilia B
20%
anemia schistocytes (bite cells) (2) G6PD deficiency, TTP
20%
anemia decreased hepcidin, increased hemosiderin hemochromatosis
20%
blood disorder autosomal recessive disorder (3) hemochromatosis, hemophilia A, hemophilia B
20%
hemophilia christmas disease hemophilia B
20%
lymphoma painless cervical/supraclavicular LAD(firm, nontender, freely mobile) Hodgkins lymphoma
20%
lymphoma contiguous spread through upper body LN Hodgkins lymphoma
20%
lymphoma pel-ebstein (cyclical) fever Hodgkins lymphoma
20%
lymphoma nodular sclerosis MC type Hodgkins lymphoma
20%
lymphoma reed sternburg cells (bilobular nucleus) Hodgkins lymphoma
20%
anemia pica, pagophagia, koilonychia iron deficiency anemia
20%
myeloma bence jones proteins multiple myeloma
20%
myeloma bone pain (spine/rib), recurrent infection, elevated calcium, anemia, kidney failure multiple myeloma
20%
myeloma punched out lytic lesions on skull XRAY multiple myeloma
20%
myeloma roleaux formation multiple myeloma
20%
myeloma > 20% myeloblasts on bone marrow biopsy myelodysplasia
20%
lymphoma painless peripheral LAD non Hodgkins lymphoma
20%
lymphoma extranodal spread to GI tract non Hodgkins lymphoma
20%
lymphoma diffuse B cell MC type non Hodgkins lymphoma
20%
anemia MCC of vitamin B12 deficiency pernicious anemia
20%
polycytosis JAK2 mutation polycythemia vera
20%
polycytosis hyperviscous blood, increased hgb polycythemia vera
20%
polycytosis facial plethora polycythemia vera
20%
polycytosis pruritus after hot bath/shower (2) polycythemia vera, CML
20%
anemia dactylitis sickle cell anemia
20%
anemia howell jolly bodies sickle cell anemia
20%
anemia valine substitution for glutamic acid on beta chain sickle cell anemia
20%
anemia frontal bossing thalassemia
20%
anemia target cells thalassemia
20%
anemia hydrops fetalis thalassemia
20%
thrombocytopenia fever, microangiopathic hemolytic anemia, thrombocytopenia, renal failure, neurological changes TTP
20%
anemia elevated homocysteine (2) vitamin B12 and B9 deficiency
20%
anemia absorbed in the terminal ileum vitamin B12 deficiency
20%
anemia paresthesias, gait abnormalities, memory loss vitamin B12 deficiency
20%
anemia elevated methylmalonic acid vitamin B12 deficiency
20%
anemia positive schilling test vitamin B12 deficiency
20%
blood disorder autosomal dominant disorder (2) von willebrand's disease, protein c deficiency
20%
leukemia overproliferation of immature WBC blasts (2) AML, ALL
0%
leukemia pancytopenia (3) AML, ALL, CLL
0%
leukemia nontender, round and freely mobile, cervical/supraclavicular LAD CLL
0%
leukemia overproliferation of mature granulocytes CML
0%
thrombocytopenia dripping blood DIC
0%
thrombophilia thrombosis, miscarriage factor v leiden
0%
thrombocytopenia normal coagulation studies (2) Factor V Leiden, TTP
0%
thrombocytopenia GP IIb/IIa receptor antibody ITP
0%
thrombocytopenia mucocutaneous bleeding, purpura, petechiae, gingival bleeding ITP
0%
myeloma plasmacytosis > 10% on bone marrow biopsy multiple myeloma
0%
myeloma increased monoclonal Ab multiple myeloma
0%
thrombophilia warfarin-induced skin necrosis protein C deficiency
0%
thrombophilia vitamin K dependent protein deficiency protein C deficiency
0%
thrombophilia purpura fulminans, thrombosis protein C deficiency
0%
thrombocytopenia decreased haptoglobulin TTP
0%
thrombocytopenia MC inherited clotting disorder von willebrand's disease
0%
thrombocytopenia mucocutaneous bleeding, petechiae von willebrand's disease
0%
thrombocytopenia prolonged PTT (3) von willebrand's disease, hemophilia A, hemophilia B
0%
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