B3-034 Introduction to RBC Disorders Flashcards
primary growth factor involved in erythropoiesis
erythropoietin
erythroids have a _________ maturation time
7 days
during erythroid maturation, the nucleus becomes
smaller and darker until it is dissolved
during erythroid maturation, the cytoplasm becomes
more pink
round, biconcave disks with central pallor
anucleate
eosinophilic cytoplasm
erythrocytes
oxygen transport
erythrocytes
total number of erythrocytes
RBC
total amount of hemoglobin
Hgb
proportion of blood occupied by RBCs
Hct
mean RBC volume/size
-cytic
MCV
average amount of hemoglobin in each RBC
MCH
average amount of hemoglobin per RBC volume
-chromic
MCHC
variation in RBC size
RDW
variation in size
anisocytosis
variation in shape
poikilocytosis
variation in size and shape
anisopoikilocytosis
immature RBCs containing residual RNA
reticulocyte
**aka polychromatic erythrocyte
circulating time of reticulocytes [increase/decreases] in anemia
increases
reticulocytes survive for _______ before becoming mature RBC
1 day
correlate with bone marrow erythropoietic activity
reticulocytes
low count of reticulocytes indicates
decreased RBC production
high count of reticulocytes indicates
increased RBC production
normal range of reticulocytes
.5-1.5% of total RBCs
measurements of anemia
Hgb, Hct, RBC
low total body red cell mass
anemia
clinical features of anemia
pallor of skin, nail beds, buccal mucosa
fatigue, weakness, malaise
dyspnea on exertion
syncope, headaches, visual disturbances
tachycardia
angina
cardiac failure
caused by inadequate or ineffective production
hypoproliferative anemia
causes of inadequate production in hypoproliferative anemia
bone marrow failure
bone marrow infiltration/replacement
nutritional deficiency
anemia of chronic disease
causes of ineffective production in hypoproliferative anemia
myelodysplastic syndromes
caused by blood loss or sequestration
anemia of blood loss
sequestration causes
splenomegaly
anemia of blood loss can be
acute or chronic
sickle cell is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic inherited
hemoglobinopathy
sickle cell