Heme Review Flashcards

(39 cards)

1
Q

Normocytic anemias

A

Anemia of chronic disease

thallassemias

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2
Q

What diseases can cause anemia of chronic disease?

A
Rheumatoid conditions
Inflammatory Bowel Disease
Cancer
Chronic infections
Chronic liver disease
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3
Q

Best lab finding for iron deficiency

A

iron to TIBC ratio of less than 10%

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4
Q

Causes of cold hemolytic anemia

A

Post mono or post mycoplasmal infection

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5
Q

Difference in immunoglobulins between warm and cold hemolytic anemias

A

IgG- warm

IgM- cold

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6
Q

Disease where sulfa drugs causes hemolytic anemia

A

G6PD deficiency

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7
Q

difference in symptoms between B12 and folate deficiencies

A

B12- neurologic findins

Folate- no neurologic findings

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8
Q

Mechanism of thallassemias

A

reduction in synthesis of globin genes

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9
Q

Best lab test of B12 deficiency

A

elevated methylmalonic acid and homocysteine

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10
Q

High iron:TIBC
Low MCV
Target cells

A

Thallassemia

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11
Q

Mechanism of anemia of chronic disease

A

Sequestration of iron in the reticuloendothelial system

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12
Q

Antibody produced in pernicious anemia

A

Anti-intrinsic factor

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13
Q

Mild anemia
High MCHC
splenomegaly
family history

A

Hereditary spherocytosis

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14
Q

Sickle cell patient

profound anemial

A

hyperhemolytic crisis

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15
Q

What infection causes sickle cell patients to have aplastic anemia

A

parvovirus B19

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16
Q

Three sickle cell complications

A

Acute chest syndrome
Salmonella ostetomyolitis
avascular necrosis of femoral head

17
Q

What vaccines should be given to a patient after a splenectomy

A

Encapsulated bacteria:
pneumoccocal
meningitis
Hib

18
Q
ruddy skin
itching
cyanosis of finger tips
splenomegaly
high platelets
A

Polycythemia vera

19
Q

Mutation present in polycythemia vera

20
Q

Complication of heparin induced thrombocytopenia

A

PE and DVT-> makes patient hypercoagulable

21
Q

AE after being on heparin for several days

A

heparin induced thrombocytopenia

22
Q

Mechanism of Paroxysmal Nocturnal Hemaglobinuria

A

Loss of GPI linked proteins on the cell surface (CD55, 59)

23
Q

History of bleeding
Elevated PTT
Increased bleeding time

A

von Willebrand’s disease

24
Q

Recent URI
petechiae on legs, arma, and trunk
profound thrombocytopenia
Normal WBC and HCT

A

Idiopathic thrombocytopenic purpora

25
Mechanism of Bernard-Soulier
platelets can't clump
26
Mechanism of Idiopathic thrombocytopenic purpora
Autoantibodies against platelets
27
``` bruises on upper and lower extremities palatal petechiae fever low HCT elevated LDH thrombocytopenia schistocytes on blood smear ```
TTP
28
``` Vertebral compression fracture high calcium kindey failure anemic high protein/albumin narrow anion gap ```
multiple myeloma
29
defect in TTP
ADAM TS-13
30
Older pt massive lymphadenopathy palpable spleen WBC 30k with lymph
CLL
31
``` High WBC (all cell lines) mild illness ```
CML
32
What is the mutation of CML
9:22 translocation of BCR-ABL proteins
33
Treatment for CML
imantinib
34
What is the mutation in acute promyelocytic leukemia
15:17, retinoic acid receptor
35
Treatment for APL
ATRA: all-trans-retinoic-acid
36
Why is calcium high in Multiple Myeloma
Osteoclase Activating factors
37
Bone biopsy finding in ITP
megakaryocytes on bone marrow biopsy
38
child bloody diarrhea followed by AKI thrombocytopenia anemia
HUS
39
Pentad of TTP
``` Microangiopathic Hemolytic Anemia Thrombocytopenia Decreased renal function Disturbed NEUROLOGICAL function: Fever ```