childhood conditions 2 Flashcards

1
Q

infx (discitis, osteomyelitis)
tumor in SC or column
trauma
-ddx for back pain in this age group

A

Pre-puberty

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2
Q
idiopathic: scheuermann's dz
tumor in sc or column
trauma
inherited
Ddx for back pain in this age group
A

puberty

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3
Q
warning signs for back pain in kids
<4yo 
functional deficiency
lasting >4w
and 4 more:
A

antalgic posture
neurological abnormalities
limited ROM
with fever

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4
Q

before MRI was available, 30% of all peds cord injuries with pos neuro findings were called:

A

SCIWORA

spinal cord injury witho out radiographic abn

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5
Q

best test for discitis, paired with s/s, hx of infx

A

bone scan

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6
Q

enuresis is not dx until this age

A

5yo

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7
Q

areas to check for enuresis

A

S2
LE, pelvis, lumbar, cervical
-myofascial release, nutrition

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8
Q

MC type of genetic obesity

A

prader willi syndrome

-chrom abn

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9
Q

MC hemolytic anemia, can cause preterm, spontaneous abortion, LBP, stillbirth, perinatal mortality

A

sickle cell anemia

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10
Q

must do this if childhood HA is: acute, worst/thunderclap, chronic and progressive, neuro sx, abn eye movements, hemiparesis, ataxia, abn reflexes, NF, heart, vomits on awakening

A

imaging

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11
Q

sudden/severe HA lasting up to 60 sec, possible sign of subarachnoid hemorrhage, trauma, stroke

A

thunderclap HA

-check T12 only

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12
Q

childhood migraine criteria

A

5+ lasting 1-48h

  • have at least 2 of: bilat/unilat, pulsating, mod-sev, exac by routine activities
  • accomp by at least 1: n/v, photo/phonophobia
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13
Q

CT autoimmune dz with polyarticular joint inflam, req davis series due to inc ADI, transverse lig instability

A

RA

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14
Q

three types of JRA
____: 5-10yo, 10%
____: 2yo, 40-60%
____: 1-3yo, 30-40%

A

systemic
pauciarticular
polyarticular

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15
Q

adult with “old” JRA

A

JCA

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16
Q

spine infx that causes rapid disc space loss, without osteophytes, DDD, pre-vert ST swelling

A

spondylitis

ddx: mets (preserved disc space)

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17
Q

4 seronegative spondyloarthropathies

(Rh-, HLA B27 +) Mc older

A

AS (MC)
PA
reiter’s
enteropathic arthritis

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18
Q

MC seroneg spondyloarthrop, and its DDX

cant see cant pee cant dance with me

A

AS

ddx: OCI
- can’t adjust bamboo spine, maybe inc ADI

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19
Q

wedging of 5* or more of 3 vert (T7, 8, 9)

A

sceuermann’s dz

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20
Q

female triad

A

osteoporosis
ED
amenorrhea

21
Q

pn at prox lat humerus, xray shows epiph widening, fragmentation, sclerosis

A

little league shoulder

22
Q

irritation/inflam/degen of shoulder tissues

A

impingement

23
Q

sulcus sign, hill sachs, bankart lesion on xray all indicate

A

shoulder dislocation

24
Q

extensor carpi radialis brevis indicated in

A

lateral epicondylitis

25
ulnar collateral ligament indicated in | -tommy john surgery
medial epicondylitis
26
ant disloc of radial head ulnar fx Together known as
Monteggia Frx
27
FOOSH can cause
scaphoid fx/disloc
28
bennett's fx is a broken:
thumb
29
ulnar collat lig of MCP 1 jt
skier's thumb | -FOOSH with abd thumb
30
AVN of met head 2
freiberg
31
AVN of navicular
kohler
32
heel pn, often in soccer
sever dz
33
boxer's/barroom fx
metacarpal 4/5 fx
34
shin splints aka
medial tibial stress syndrome
35
pars defect/frx w/o anterior slippage, 90% L5, MC white males scottie dog
spondylolysis
36
MC type of spndylolisthesis
isthmic
37
``` spondys I II III IV V ```
``` dysplastic *5* isthmic *MC* traumatic degenerative *L4* pathologic ```
38
MC type of salter harris frx, thurston hollon sign | above epiphys plate
type 2 (A)
39
salter harris phys frx straight across the epiphs plate
type 1 (S)
40
older children, salter harris frx, starts thru GP and goes beLow
type 3 (L)
41
salter harris goves starts above GP and exits Thru joint cartilage
type 4 (T)
42
growth plate crushed in salter harris frx, most concerning prognosis (ERasure of gp)
type 5 (ER)
43
4 stages of AVN | avascular -> ____ -> repair -> _____
revascularization | deformity
44
subchondral bone collapse on xray is seen in ____ sign and the healing phase with osteoblastic activity in a fuzzy mushy appearance is ___ sign
crescent | snow cap
45
PLASTICRAGS acronym for avn(?)
``` Pancreatitis/preg LCP, lupus Alcoholism/atherosclerosis Steroids Trauma Idiopathic/infx Caisson/collagen dz RA/radiation Amyloid Gaucher dz Sickle cell anemia ```
46
segmental AVN presents with clicking, locking, limited ROM, swelling, pn on ROM, floaters
OCD
47
MCC of BP in athletic teenages
facet tropism
48
_____ is assoc with klippel feil and arnold chiari malform, scap winging
sprengel's deformity
49
MCC of death in children
accidents