Heme/Onc/Immuno Flashcards

1
Q

milk related Fe deficiency

what is this:

how to tx

A

Too much cow’s milk, very common.

all children born with Fe stores for 6 months. Sxs of Fe deficiency may not develop until 10 months, usu dx is 1-2y

>24-32oz cow’s milk with no other foods (OR exclusive breast feeding)can cause microscopic bleeding from GI tract, with inhibition of Fe absorption

Labs: Hgb as low as 2

Tx: elemental Fe 3-6mg/day, limit cows milk

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2
Q

Transient erythroblastopenia of childhood

what is this

A

possible parvovirus onfection

red cell aplasia, with hgb 5-7, low retic count, normal MCV

dx around age 2

no tx, resolves in 1-2 mo

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3
Q

von willibrands disease

what labs

A

elevated PTT, decreased factor 8 level

reduced VWF

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4
Q

hemophilia

PT/PTT shows what?

how to tx:

A

PTT elevated, normal PT

CNS bleed: correct to 100% factor level

joint/muscle: correct to 50% except psoas muscle

Oral: one dose of factor (30-50%), and amicar

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5
Q

hemophilia

what factor level % indicates severe?

A

>1% is severe

1-5% is moderate, can have spontaenous bleed

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6
Q

leukemia:

sanctuary sites

A

CNS and testes

pts with known leukemia can have recurrence in these sites

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7
Q

child with neck pain/torticollis

what to think of

A

herniation of cerebellar tonsil from high ICP, eg tumor

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8
Q

Peds brain tumor

how sensitive is CT

A

65-100%?

can miss glioma, esp in infratentorial locations

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9
Q

opsoclonus myoclonus

what is this and what is significance

A

asymmetric jumping mvments of eyes, with myoclonic jerks

think of neuroblastoma (paraneoplastic syndrome)

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10
Q

Pt with raccoon eyes, but no hx of trauma and not abuse

think what

A

mets to skull/eye of neuroblastoma

looks like abuse

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11
Q

osteosarcoma vs ewings

radiologic classic findings

A

osteosarcoma “sunburst”

ewings “onion peel”

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12
Q

neutropenic fever strict definition:

  1. neutropenia count
  2. fever
    - what empiric abx?
A
  1. ANC <1000
  2. fever >38.3, OR 2 separate temps 4h apart of >38.0
    - 3rd gen ceph (eg cefepime), gent, vanc
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13
Q

tumor lysis electrolytes:

  • what 4 to know, high/low
  • tx
A

K high

Phos high –danger to renal, use phosphate binder, ivf

Ca low (binds phos)– replete if necessary (eg tetany)

Uric acid high–danger to renal, tx with rasburicase, ivf, prevent with allopurinol

Tx based on electrolytes above

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14
Q

sickle cell pain crisis

how to hydrate

A

be careful about pulm edema

hydrate 1.5x maintenance, don’t bolus

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15
Q

sickle cell dactylitis

-how to tx

A

treat as pain crisis, can dc home with analgesia

lasts days-week

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16
Q

sickle cell RUQ pain

think what things?

A
  1. gallstones
  2. hepatic sequestration
  3. intrahepatic cholestasis: sudden pain, jaundice, anorexia, tender hepatomegaly, fever, high bili
17
Q

splenic sequestration:

what age?

A

age <5 years in HbSS. usu by 6 months

However, HbSC may have splenic infarcts later in life

18
Q

Fever in sickle cell:

management, discharge home?

A

Age <1y: ceftriaxone, admit

Age 1-5: ceftriaxone, dc with 24h f/u if low risk criteria:

temp<40, wbc 5-30, plt>100, hgb >5, cxr normal, well appearing, no hx of pneumococcal sepsis

age 5+: most stable pts can go home

19
Q

HSP

what to check in urine

A

linked to IGA nephropathy

check for: hematuria, protein, casts

check Cr

90% of patients that develop renal dz do so within 2 months. f/u very important

20
Q

kawasaki criteria

-classic def, vs incomplete

A

Fever >38.5 x5d and 4/5 criteria

CRASH and burn

conjunctivitis (limbic sparing), rash (can be any type), adenopathy (nontender), strawberry tongue (mucositis), hands/soles skin sloughing

incomplete form: fewer criteria or <5d

21
Q

Kawasaki’s, incomplete form

how to manage/dispo

A

Do labwork. if 3 abnormal labs, continue further testing and admit

labs: WBC, crp, esr, platelets, ALT
- admit: get echo, consult ID