Pediatrics Flashcards

1
Q

Cloverleaf skull ddx

A
  • thanatophoric dysplasia
  • Apert syndrome (brachycephaly, syndactyly
  • Crouzon syndrome (brachycephaly, 1st arch structures maxilla/mandible hypoplasia, hydrocephalus, Chiari 1, coarctation, rhizomelia short central bones, exophthalmos)
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2
Q

Agenesis of the corpus callosum associations

A
  • Dandy-Walker spectrum
  • hydrocephalus
  • Chiari Il malformations
  • encephaloceles
  • porencephaly
  • holoprosencephaly
  • polymicrogyria
  • trisomy 13, 15, and 18
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3
Q

Double bubble sign ddx

A
  • duodenal atresia
  • annular pancreas
  • obstruction by Ladd’s bands
  • midgut volvulus
    additional imaging evaluation with upper GI series is needed if the patient has a noncharacteristic clinical presentation.
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4
Q

absent cavum septum pellucidum ddx

A
  • congenital hydrocephalus
  • hydranencephaly
  • porencephaly
  • holoprosencephaly spectrum
  • schizencephaly
  • Chiari 2 malformation

Cavum septum pellucidum is always visualised between 18 and 37 weeks. Closes after 37 weeks as septum pellucidi fuse in most people.

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5
Q

lemon skull ddx

A

Chiari 2 malformation +/- spina bifida

think of the frontal bones being pinched, squeezing cerebellum out foramen magnum, and popping spinal canal contents out the back of the spine

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6
Q

banana cerebellum ddx

A

Chiari 2 malformation +/- spina bifida

think of the frontal bones being pinched, squeezing cerebellum out foramen magnum, and popping spinal canal contents out the back of the spine

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7
Q

radial ray malformation ddx

A
  • VACTERL association
  • trisomy 18 (Edward syndrome, look for rocker bottom feet, choroid plexus cysts)
  • diabetic embryopathy
  • isolated
  • Holt-Oram syndrome: Cardiac septal defects with upper extremity abnormalities
  • thrombocytopenia-absent radius (TAR) syndrome: Thumbs are present
  • Fanconi anemia
  • teratogens: Valproic acid
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8
Q

Nasal lesion in an infant ddx

A
  • nasal glioma (extend through patent foramen cecum in ant cranial fossa, but separate from brain tissue, nonenhancing, diffusion restrict)
  • nasal dermoid/epidermoid (nonenhancing, may contain fat)
  • infantile hemangioma (vascular)
  • encephalocele
  • dacrocystocele
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9
Q

Big f#cking mass in the abdomen ddx (child)

A
  • neuroblastoma
  • nephroblastoma
  • lymphoma
  • hepatoblastoma
  • mesenchymal hamartoma
  • sarcoma
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10
Q

Choanal atresia associations

A
  • CHARGE (coloboma, heart defect, atresia of choana, retarded growth, genitourinary anomalies, ear anomalies)
  • Crouzon
  • DiGeorge
  • Treacher Collins
  • fetal alcohol syndrome

CHARGE syndrome most common association

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11
Q

Pediatric chest tumor ddx

A
  • inflammatory myofibroblastic tumor (aka inflammatory pseudotumor, benign, most common primary lung mass, calcified, lower lobe, T2 bright myxoid)
  • Neuroblastoma (posterior mediastinum, calcify, MIBG avid)
  • Ewing sarcoma (includes Askin tumor)
  • Pleuropulmonary blastoma (can look like CPAM, involve pleura, don’t invade chest wall)
  • lymphoma
  • rhabdomyosarcoma

Remember, however, that a round density in the lung parenchyma on CXR is almost always round pneumonia in kids, and a common trick to make you call a mass lesion

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12
Q

neonatal bowel obstruction (proximal) ddx

A
  • malrotation w/midgut volvulus
  • duodenal atresia, web, annular pancreas
  • jejunal atresia
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13
Q

neonatal bowel obstruction (distal) ddx

A
  • Hirschprung disease
  • meconium plug syndrome
  • meconium ileus
  • ileal, colonic, anal atresia
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14
Q

Abdominal pain in an older child ddx

A
  • appendicitis (and its mimic mesenteric adenitis)
  • adhesions
  • intussusception
  • inguinal hernia
  • Meckel diverticulum
  • midgut volvulus
  • distal intestinal obstruction syndrome (adults and kids non compliant with pancreatic enzymes)

things to think about when reviewing any imaging…

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15
Q

Intramedullary spinal cord mass ddx

A
  • ependymoma (hemosiderin caps)
  • astrocytoma (identical imaging to ependymoma)
  • lymphoma
  • hemangioblastoma
  • cavernoma

always assess relationship to dura and spinal cord to place tumor and narrow ddx

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16
Q

Intradural extramedullary mass ddx

A
  • epidermoid cyst
  • lipoma
  • meningioma (extramedullary, homogenous, calcifies)
  • schwannoma (extramedullary dumbell, widens neural foramen)
  • neurofibroma

always assess relationship to dura and spinal cord to place tumor and narrow ddx

17
Q

Pediatric liver cirrhosis ddx

A
  • biliary atresia
  • Fanconi syndrome
  • glycogen storage disease
  • cystic fibrosis (in 10%, in first decade)
  • Wilson disease
18
Q

Prolonged newborn jaundice ddx

A
  • neonatal hepatitis
  • biliary atresia (need corrective surgery before 3 months)
19
Q

Wilms associated syndromes

A
  • hemihypertrophy
  • hypospadias
  • cryptorchidism
20
Q

Child with ‘raccoon eyes’ ddx

A
  • base of skull fracture (trauma/NAI)
  • neuroblastoma mets (95% dx < 10 yrs)
  • leukemia/lymphoma (extremely rare)

older: Kaposi sarcoma, multiple myeloma, and amyloidosis

21
Q

Periosteal rection (child) ddx

A
  • trauma / NAI, (seen reliably 7-10 days post injury)
  • physiologic periostitis of the newborn (actually occurs >1mo, sus if earlier, always involves diaphysis and femur before tibia)
  • prostaglandin E1/2 therapy for PDA
22
Q

Lucent metaphyseal bands ddx

A
  • leukemia
  • lymphoma
  • infection (TORCH)
  • neuroblastoma mets
  • endocrine (Rickets)
  • scurvy

“Lucent LINES”

23
Q

Expanded costochondral junctions (kids) ddx

A
  • Rickets (rachitic rosary)
  • scurvy (scorbutic rosary, more agular and sternum often depressed also)
  • hypophosphatasia
  • healing fractures (NAI)
24
Q

Caudal regression syndrome associations

A

VACTERL
- vertebral
- anogenital
- cardiac
- trache-Esophageal fistula
- renal
- limb/radial ray

Currarino triad
- anterior sacral meningocele
- anorectal malformation
- sacrococcygeal defect (scimitar sacrum)