Peds Heme/Onc Flashcards

1
Q

Neutrophilia with lots of bands (>700)

A

neonatal sepsis

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2
Q

kidney disease associated with HIV

A

FSGS - most common nephrotic syndrome in adults

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3
Q

Hep B kidney disease

A

Membranous nephropathy (nephrotic)

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4
Q

pre-adolescent kidney disease

A

minimal change disease

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5
Q

PSGN

A

nephritic

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6
Q

Blood transufsions what electrolyte abnormality

A

Fe overload

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7
Q

Reticulocyclopenia

from what infx

A

sudden arrest of erythropoesis

parvo B19

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8
Q

Hemophilia A &B inheritance patten

A

X-linked recessive

usually males

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9
Q

Parvo risk in sickle cell

A

aplastic anemia

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10
Q

Shield Chest

A

Diamond Blackfan,
Noonan
Turner Syndrome

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11
Q

ITP tx

A

glucocorticoids or IVIG

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12
Q

Wiskott Aldrich triad

A

X-linked disorder with

  1. thrombocytopenia
  2. eczema
  3. recurrent bacterial infx
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13
Q

ALL

A

Hepatospleenomegally
lymphadenopathy
petichiae

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14
Q

nasal obstruction with visible mass
bony errosion
epistaxis

A

Juvenile angiofibroma

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15
Q

Juvenile angiofibroma

A

nasal obstruction with visible mass
bony errosion
epistaxis

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16
Q

renal failure
hemolytic anemia
thrombocytopenia

s/p diarrhea

A

Hemolytic Anemia

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17
Q

Diamond Blackfan anemia vs. Megaloblastic

A

Both are Macrocytic

Diamond Blackfan results in no hypersegmentation of nucleus in neutrophils

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18
Q

Macrocytic Anemia with Congenital anomalies and low retic count

A

Diamond Blackfan anemia

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19
Q

Diamond Blackfan anemia tx

A

corticosteroids/ transfusions

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20
Q

Wiskott-Aldrich inheritence

21
Q

Eczema
Low Platelets
Hypgammaglobulinemia

A

Wiskott-Aldrich

22
Q

Red Cell Aplasia

A

Transient Erythroblastopenia

23
Q

Pancytopenia and Macrocytosis and

Cafe Au Lait spots, microcephaly, horshoe kidneys, no thumbs (not triphalangeal thumbs)

24
Q

Fanconis

A

Pancytopenia and Macrocytosis and

Cafe Au Lait spots, microcephaly, horshoe kidneys, no thumbs (not triphalangeal thumbs)

25
Fanconi's age
8 years
26
Diamond Blackfan anomalies
Sheild Chest, Triphalangeal thumbs, short with webbed neck and cleft lip
27
Heinz bodies
hemoglobin precipitates... found in G6PD deficiency
28
low Retic
Fe def, B12 def, chemo, infx, aplastic anemia
29
neonatal polycythemia
delayed clamping of umbilical cord May cause respiratory distress, hypoglycemia Hct>65%
30
Leukocytosis Anemia Thrombocytopenia
ALL Pain insidious and worse at night
31
Pancytopenia after drugs or toxin exposure or viral infections
Aplastic Anemia
32
``` anemia hyperpigmentation on trunk and intertrigenous areas cafe au lait short stature hypogonads renal changes eyelid changes ```
Fanconis Thrombocytopenia is first then neutropenia then anemia
33
Diamond Blackfan age
first 3 months of life
34
Transient Erythroblastopenia of Childhood (TEC)
acquired aplastic anemia gradual pallor and tachycardia normocytic normochromic anemia
35
prolonged aPTT but not PT in newborn
Factor 8 def (similar to vWD)
36
mucocutaneous bleeding petechiae normal PT, normal aPTT
uremia aspirin/clopidogrel Glanzmann throbasthenia congenital disorder
37
MCC inherited bleeding d/o
von Willebrand dz may present similar to Factor 8 def
38
prolonged PT and aPTT in newborn
think Vitamin K def
39
hypochromic microcytic anemia with family hx
Alpha Thal
40
hypochromic microcytic anemia from 6-12 months
Beta Thal
41
Hemophilia A
Factor 8
42
Hemophilia B
Factor 9
43
Fe deficiency vs. spherocytosis
Fe deficiency has increased RDW
44
vitamin K clotting factors
2, 7, 9, 10, Protein C, Protein S
45
how to diagnose ALL
bone marrow biopsy
46
Anisocytosis
red blood cells of different size common in Fe def. anemia
47
what is normal level of reticulocytes
0.5% - 1.5%
48
low retic vs. high retic
low retic = leukemia or infection or aplastic anemia high retic = hemolysis or maybe hemorrhage