ch 11 pt 1 Flashcards

1
Q

formation and development of blood cells

A

hematopoiesis

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2
Q

extramedullary hematopoiesis can mets to these 4 locations

A

spleen
liver
lymph nodes
thymus

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3
Q

rupture of RBC, releases hemoglobin into circ

A

hemolysis

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4
Q

erythrocyte (RBC) production increased if needed

-compensatory hyperplasia of rbc stem cells in red bone marrow

A

erythropoiesis

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5
Q

immature RBC (1-3% of them in circ)

A

reticulocyte

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6
Q

increased RBC in circulation

A

polycythemia

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7
Q

deficiency of rbc is anemia, with prevalence in the US __% of men and __% of women

A

4%

8%

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8
Q

anemia prod tissue hypoxia, with increased ______ via kidneys and increased ____ from renal fibrolasts

A

erythropoiesis

erythropoietin

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9
Q

pallor, fatigue, weakness (lassitude, decreased growth, osseous abnorm, cachexia, jaundice, gallstones can all occur with:

A

anemia

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10
Q

____ anemia can follow burns, internal GI injuries, diarrhea, gyno probs, and puts a pt at risk for hypovolemic shock if >20% BV is lost

A

hemorrhagic

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11
Q

in renal hypoxia there is increased EPO, and ___ occurs after 2-3 days, then ____ after 5-7

A

hemodilution

reticulocytosis

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12
Q

chronic blood loss following anemia can deplete iron stores req for ____ synth

A

hemoglobin

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13
Q

___ anemias cause accel rbc destruction

  • decreased rbc life span
  • increased erythropoiesis
  • retention of rbc debris (iron)
A

hemolytic

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14
Q

____ defects are hereditary, inside the cell, and decrease rbc life, leading to hemolytic anemia

A

intracorpuscular

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15
Q

___ defects are AQUIRED, outside the cell, involve rbc trauma or infections

A

extracorpuscular

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16
Q

hemolytic anemia caused by trauma to rbc membrane

-periph blood syst

A

intravascular hemolysis

17
Q

hemoglobin in urine, can cause jaundice/hemosiderinuria (brown urine due to hb)

A

hemoglobinuria

18
Q

hemolytic anemia that is MC, and has macrophages in the spleen and liver, rbc damage, antibody opsonization

A

extravascular hemolysis

19
Q

autosomal dominant mutation with a fragile, abnormal RBC membrane - causing it to be less elastic and therefore sheds pieces
-decreased life span

A

hereditary spheriocytosis

20
Q
  • spherical RBC, after becoming less elastic

- are dark red, lack central pallor

A

spherocyte

21
Q

treatment for hereditary spherocytosis

A

splenectomy

22
Q

sickle cell anemia is due to a ___ mutation

A

B-globin

23
Q

__% of african americans are HETEROzygous or carriers, while 1:____ are HOMOzygous, who have sickle cell anemia, only 50% survive >50 yo

A

8

600

24
Q

in sickle cell anemia, decreased ___ causes sickling, which causes microvascular ______
-esp in areas of STASIS ie bone marrow, spleen

A

O2

thrombosis

25
Q

2 symptoms of sickle cell anemia

A

chronic low-level pain

joint pain

26
Q

lung infections/PE that occurs with sickle cell anemia and can lead to thrombosis eventually

A

acute chest syndrom

27
Q

___ can occur with sickle cell anemia due to cerebrovascular obstruction

A

stroke

28
Q

vertebral involvement in sickle cell anemia

A

H shaped (lincoln log) vertebrae