ch 11 pt 1 Flashcards
formation and development of blood cells
hematopoiesis
extramedullary hematopoiesis can mets to these 4 locations
spleen
liver
lymph nodes
thymus
rupture of RBC, releases hemoglobin into circ
hemolysis
erythrocyte (RBC) production increased if needed
-compensatory hyperplasia of rbc stem cells in red bone marrow
erythropoiesis
immature RBC (1-3% of them in circ)
reticulocyte
increased RBC in circulation
polycythemia
deficiency of rbc is anemia, with prevalence in the US __% of men and __% of women
4%
8%
anemia prod tissue hypoxia, with increased ______ via kidneys and increased ____ from renal fibrolasts
erythropoiesis
erythropoietin
pallor, fatigue, weakness (lassitude, decreased growth, osseous abnorm, cachexia, jaundice, gallstones can all occur with:
anemia
____ anemia can follow burns, internal GI injuries, diarrhea, gyno probs, and puts a pt at risk for hypovolemic shock if >20% BV is lost
hemorrhagic
in renal hypoxia there is increased EPO, and ___ occurs after 2-3 days, then ____ after 5-7
hemodilution
reticulocytosis
chronic blood loss following anemia can deplete iron stores req for ____ synth
hemoglobin
___ anemias cause accel rbc destruction
- decreased rbc life span
- increased erythropoiesis
- retention of rbc debris (iron)
hemolytic
____ defects are hereditary, inside the cell, and decrease rbc life, leading to hemolytic anemia
intracorpuscular
___ defects are AQUIRED, outside the cell, involve rbc trauma or infections
extracorpuscular
hemolytic anemia caused by trauma to rbc membrane
-periph blood syst
intravascular hemolysis
hemoglobin in urine, can cause jaundice/hemosiderinuria (brown urine due to hb)
hemoglobinuria
hemolytic anemia that is MC, and has macrophages in the spleen and liver, rbc damage, antibody opsonization
extravascular hemolysis
autosomal dominant mutation with a fragile, abnormal RBC membrane - causing it to be less elastic and therefore sheds pieces
-decreased life span
hereditary spheriocytosis
- spherical RBC, after becoming less elastic
- are dark red, lack central pallor
spherocyte
treatment for hereditary spherocytosis
splenectomy
sickle cell anemia is due to a ___ mutation
B-globin
__% of african americans are HETEROzygous or carriers, while 1:____ are HOMOzygous, who have sickle cell anemia, only 50% survive >50 yo
8
600
in sickle cell anemia, decreased ___ causes sickling, which causes microvascular ______
-esp in areas of STASIS ie bone marrow, spleen
O2
thrombosis
2 symptoms of sickle cell anemia
chronic low-level pain
joint pain
lung infections/PE that occurs with sickle cell anemia and can lead to thrombosis eventually
acute chest syndrom
___ can occur with sickle cell anemia due to cerebrovascular obstruction
stroke
vertebral involvement in sickle cell anemia
H shaped (lincoln log) vertebrae