Anemias Flashcards

1
Q

Spherocytosis

A

Defect in ankyrin
Hyperchromic, extravascular, hemolysis

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2
Q

Elliptocytosis

A

Defect in spectrin
Protective against malaria

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3
Q

PK deficiency

A

Decreased ATP, increased 2,3BPG, rigid RBC
Normocytic normochromic

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4
Q

G6PD deficiency

A

Decreased NADPH, decreased GSSG and increased ROS - damage

Heinz bodies, episodic

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5
Q

PNH

A

Defect in PIGA/GPI anchor/CD55&59

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6
Q

March hemoglobinuria/foot strike

A

Trauma from running, small blood vessels

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7
Q

WAIHA

A

IgG ran with Rh at 37 degrees
Extravascular
IgG+
Decreases platelet, microspherocytes

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8
Q

CAD

A

Type of CAIHA
Can be extravascular or intravascular
C3 and IgM positive

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9
Q

DAT/Coombs test

A

Anti IgG and anti C3 - immune mediated

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10
Q

PCH

A

Kids with respirator infection, dark urine

Intravascular
C3+

Biphasic IgG activates complement in cold and dissociates in warm so only C3 positive

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11
Q

Drug induced

A

Antibiotics - IgG - extravascular
Quinidine - C3+ - intravascular

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12
Q

Iron deficiency anemia

A

Microcytic, normochromic

Decreased Fe, serum ferritin (less storage), % transferrin (not much iron to bind)
Increased TIBC (body trying to scavenge more)

Low hepcidin

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13
Q

Hepcidin

A

Inhibits iron absorption

Hi - no iron absorbed
Lo - iron absorbed

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14
Q

Thalessemia

A

Microcytic, hypochromic

Decreased RBC, Hb, erythropoiesis

Decreased ferritin

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15
Q

Sideroblastic anemia

A

Hereditary

No heme, but excess free iron, ring sideroblasts

Increased iron, decreased TIBC, increased % transferrin, increased ferritin

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16
Q

Anemia of chronic disease

A

Mild hypochromic, microcytic

Decreased Fe, TIBC, % transferrin, increased ferritin

Presence of IL-1 & TNF can decrease EPO

17
Q

Megaloblastic anemia

A

Macrocytic anemia
Larger, oval, hyperhsegmented nucleus
Decreased reticulocytes
Can be caused by B12 or B9 deficiency

18
Q

B12 deficiency

A

B12 from diet absorbed in ileum
Build up of MMA and homocysteine

19
Q

Pernicious anemia

A

Autoimmune attack of IF, decreased B12

20
Q

B9 deficiency

A

B9 absorbed in SI
Needed for purine and pyrimidines
Build out of homocysteine

21
Q

Sickle cell anemia

A

Normocytic, bite cells

Vasoocclusion pain crisis, ischemia, acute chest syndrome, splenic sequestration

Treat with hydroxyurea (increases HbF)

22
Q

Alpha thalassemia

A

Silent, trait/mild, disease , hydrous fetalis

Causes HbH = B tetramers

Some HbBarts = Y tetramers - hemolytic

23
Q

Beta thalassemia

A

Carrier - intermediare - major = Cooley’s, transfusion dependent

Symptomatic at 3 months when HbF drops

Increased EPO - bone deformation