Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
44 Cards in this Set
- Front
- Back
what is a macrocyte?
|
RBC > 8 micrometer in diameter
|
|
what is hemoglobin S
|
HbS (S=sickle) is the abnormal variant of hemoglobin A, which occurs in sickle-red blood cells
|
|
Two coagulation tests excluding BT and PTT
|
-Platelet count
-coagulation time -fibrinogen, -thromboplastin time |
|
tests done in hematology excluding CBC, ESR and coagulation
|
-sickle cell test
-LE cell -eosinophil count -hemoglobin electrophoresis -leukocyte alkaline phosphatade |
|
one thrombin sensitive coagulation factor
|
-fibrinogen factor 1, 5, 8, 13
|
|
one disease in which ESR is high
|
-rheumatoid arthritis
-SLE -MI -Lyme |
|
disease in which normoblastosis is seen
|
-pernicious anemia
-folic acid deficiency |
|
disease in which PLT functionis affected
|
Bernard-soulier syndrome
|
|
3 characteristics of an immature blood cell
|
-big size
-big, round, oval, or slightly indented nucleus and relatively large in relation to the cytoplasm -blue cytoplasm (high amount of RNA w/ affinity for blue dyes) -red nuclear chromatin (due to the DNA w/ affinity for acidophilic red dye -visible strands of nuclear chromatin -visible nucleoli -presence of primary granules |
|
the 3 most immature neutrophils by order are
|
myeloblast, promyelocyte, myelocyte
|
|
hemophilia is characterized by
|
Normal BT and high PTT
|
|
HbA2 migrates together with HbC and _____ in alkaline pH
|
HBE
|
|
The priniciple Ags of the ABO system are
|
O, A, and B
|
|
2 blood systems excluding ABO, Rh, and MNS are
|
-Kells
-duffy |
|
the test that differentiates b/n immune and non-immune hemolytic anemia is
|
indirect coombs test
|
|
T/F Osmotic fragility test is decreased in hereditary sphero-cytosis
|
F
|
|
t/f parahemophilia is deficiency of factor 7
|
F (its factor 5)
|
|
t/f PTT evaluates the intrinsic system
|
T
|
|
t/f A leukemia is acute when more than 50% of blasts are seen in bone marrow
|
F
|
|
t/f the 3 most common abnormal hemoglobin are S, E, and D
|
F (it's SCE in US)
|
|
t/f factor 5 is called proaccelerin
|
T
|
|
what disease do u see lymphocytosis?
|
whooping cough, viral infection, measles/mumps
|
|
wat disease do u see in neutropenia?
|
coppers deficiency, gaucher disease
|
|
wat disease do u see in thrombocytosis?
|
RA/TB
|
|
what disease do u see in high PTT but normal PT
|
VWD
|
|
hemoglobin CC disease associated with
|
codocytes
|
|
lead poisoning is associated with
|
basophilic stippling
|
|
multiple myeloma is associated with
|
rouleaux
|
|
sickle cell anemia is associated with
|
drepanocytes
|
|
thalassemia is assocated with
|
hypochromia
|
|
vitamin B12 deficiency is associated with
|
macrocytes
|
|
which coagulation factor deficiencies are not related with hemorrhagic manifestations? how are they usually inherited?
|
-contact factors, 11, 12, hmwk, fletcher
-autosomal recessive |
|
wat is seen in aplastic anemia?
|
dohl bodies
|
|
wat is seen in human monocytic ehrlichiosis?
|
vavuolated monocytes
|
|
wat disease would u see in thrombocytopenia?
|
Aplastic anemia
|
|
wat disease would u see High ESR
|
TB
|
|
wat disease would u see high PTT and normal PT
|
VWD
|
|
name the coagulation factors that are thrombin sensitive
|
1, 5, 8, 13
|
|
name the coagulation factors that are vit K dependent
|
2, 7, 9, 10
|
|
name the coagulation factors that are contact factors
|
11, 12, HMWK, fletcher
|
|
name the intrinsic coagulation factors
|
8, 9, 11, 12 (hageman), HMWK, fletcher
|
|
name the extrinsic factors
|
2, 7
|
|
name the common coagulation factors
|
5, 10
|
|
serum does not contain wat coagulation factors?
|
1, 2, 5, 8, 13 (only 7, 9, 10)
|