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84 Cards in this Set

  • Front
  • Back
Chest
Stridor, wheezing
Upper airway obstruction
Tracheal lesions
Rings and slings
Foreign bodies
Asthma
Upper airway obstruction
Inflammation: epiglottitis, croup, retropharyngeal abscess
Exogenous: caustic ingestion, foreign body
Extrinsic upperairway compression: thyroglossal duct cysts, branchial cleft cysts, other masses
Bubbly lungs in neonates
BPD
Poumonary interstitial emphysema
Cystic fibrosis
Wilson-Mikity syndrome
Mass lesions in airways
Lymphangioma hemangioma occur anywhere
Nasal cavity: antrochoanal polyp, meningoencephalcele, angiofibroma, lymphadenapthy, neuroblastoma, rhabdomyosarcoma
Oropharynx: lymphadenapthy, ectopic thyroid tissue
Hypopharynx: retention cyst, papillomas
Neonatal lung masses
Lung bases, CPA
Sequestration
CDH
CCAM
Hypoplstic lung (scimiatar synrome)
Phrenic nerve paralysis:elevation of hemidiaphrgm
Neonatl lung masses
Not lung bases, other lung zones
Pulmonary tumor(neuroblastoma, pulmonary blastoma, PNET (ASKIN)
Congenital lobar emphysema (early in disease)
Hyperlucent lung
anterior pneumothorax
CLE
Congenital lung cyst
Bronchiolitis obliteran (Swyer james )
Obstructive emphysema (cystic fibrosis, astma, pneumona, foreign body, extrinsic comression (rings, slings, adenapathy, bronchogenic cyst
CCAM
Neonatal pneumothorax
Pressure ventilation
Interstitial pulmonar empysema
Pulmonary hypoplasia ( felat anuria, potter sequence, oligohydramnios)
Small solitary pulmonary nodule
Congeital: bronchgenic cyst, sequestration, AMV, varix, bronchial atresia
Infection: round pneumonia, granuloma, abscess cavity
Tumor: PNET, pulmonary blastoma, neuroblastoma, wilms
Multiple pulmonary nodules
TUmor: mets. laryngeal papillomatosis
Infection: septic emboli, tb, fungus
Inflammatory: Wegener's disease
pediatirc interstitial pattern
congenital (strage disease: gauchers neimannn pick)
Other: viral pneumona, BPD, RDS, histiocystosis X
Pediatric chest wall tumors
EG
Askin tumor (PNET)
neuroblastoma
mets
Ewings sarcoma
Dilated stomach
Normal gas (crying)
hypertrophic pyloric stenosis
Pylorospasm
Antral web
Antral gastritis
Rare: duplication cyst, ectopic pancreatic tissue, polyps, neoplasm
Double bubble
duodenal atresia
annular pancreas
Duodneal diaphragm bands
Midgut volvulus
Vascular (preduodenal vien, SMA syndrome)
Rare duplication cysts, adhesions
Proximal bowel obstruction
Noenates: atresia, midugt volvulus, ladd bands
Children: intussusception, incarcerated inguinal hernia, perforated appy
Distal bowel obstruction
Hirschsprungs disease meconium plug syndrome colonic atresia/stenosis imperfoate anus
meconium ileus
Rare: volvulus, presacral tumors, post NEC strictures
Microcolon
Diabetic mother
Maternal Mg SO4 use
Unused colon (no fecal material or succus has passed, ileal atreisa, meconium ileus)
Total colonic Hirschsprungs disease
Pediatric pneumoatosis intestinalis
NEC
Less common: cystic fibrois, CVD, leukemia, Milk intolerance, immunodeficiency)
Obstruction
steroid use
Gasless abdomen
Gastroenteritis
Appendicitis
Espohageal atresia
Neurologic impairment
Mechanical ventilation
Displaced bowel loops
bowel not in abdomen( hernia, omphalocele, etc)
Masses
Ascites
Abdominal calcifications
Intraabdominal: meconium peritonitis
Renal: neuroblastoma, wilms, nephrocalcinosis, renal cysts, urinary tract calc
Bowel: fecalith, meckel dieveticulum
Bladder: hemorrhagic cystitis (cytotoxan)
Adrenal: hemorrhage, Wolman's disease
Liver: hepatomblastoma, granuloma
Common ABdominal mass lesions
Neonates
Renal: hydronephrosis, MCDK
GI: duplication, meconium pseuodcyst, pseudo cyt proxiaml to atresia
GU: ovarin cyst, hydrometrocolpos
Heptobiliary: hemangioendothelialioma, choledochal cyst
Common ABdominal mass lesions
Older infants and children
Renal: wilms, hydronephrosis
GI: append, abscess, intussusception, neoplasm
Retroperitoneal: neuroblastoma
GU: ovarian cyst, hydrometrocolpos
Hepatobiliary: hepatoblastoma
Gastric filling defect
foreign body
Bezoar
Congenital anomalies (duplications, ectopic pancreatic tissue)
Inflammation: crohns, chronic granulomatous diseases
Tumors: hamartoma, peutz jegher disease
Thick folds
Submucosal edema
submucosal tumor (lymphoma, leukemia)
Submucosal hemorrhage (henochschonlein purpura, HUS, coagulopathies)
GI hemorrhage
meckel diverticulm
Juvenile polyps
IBD
Portal hypertension
Pediatric liver lesions
Benign: cyst, hemangioendolthelialioma, mesenchymal hamartoma
Malig: hepatoblastoma,hemangioendolthilioma, HCC, mets
Fatty liver
Chronic protein malnutrition
Congenital (Cystic fibrosis, glycogen storage disease, wilsons disease, galactosemia, fructose intlorance, reye's syndrome
Hepatitis
Drugs: chemotherapy, steroid, hyperalimentation
Pediatric choleliatiasis
Hemolyis: sickle cell, thalasemia, spherocytosis
Other: cystic fibrosis, drugs(lasix), metabolic diorders (hyperparathyroidsim), premature infants with RDS
Hydrops of gallbladder
Sepsis
Burns
Leptospirosis
Kawaski disease
Cholecystitis
sickle cell
anemia
Biliary strictures
pancreatitis
gallstones
ascending cholangitis
Post kasai procedure
Liver transplant
Fatty replacement of pancreas
Cystic fibrosis
Schwachman Diamond syndrome (metaphyseal dysplasia, cyclic neutropenia, pnacreatic fatty replacement, flaring of ribs)
Pediatric pancreatitis
trauma
viral infection
Sepsis
Idiopathic
anomaly
drugs
metabolic (cystic fibrosis, hyperlipidemia)
Cystic renal masses- cystic disease
ARPCKD- hyperechoic enlarged
MCDK - atretic ureter and artery, no functional parencyma
Multilocular cystic nephroma- very large cysts
Phadomatosese- VHL, TS
Tumors- cystic wilms, cystic adenocarcinoma
Hydronephrosis
Reflux
UVJ obstruction
Ureterovesical obstruction
Ectopic ureterocele
Posterior urethral valves
Prune belly
Solid renal masses
Wilms tumor
Mesoblastic nephroma: only solid mass in newborns
Nephroblastomatosis:subcortical
Angiomyolipoma: fatty mass, a/w TS
Secondary: lyphoma, neuroblastoma, leukemia
Rare renal tumors: clear cell sacrcoma, malignant rhabdoid, RCC
Diffusely hyperechoic renal kidney in newborn
Increased size: ARPCKD, CMV, glomerular cystic disease, diffuse cystic dysplasia
Decreased size: renal dysplasia form obstructive uropathy or necrosis
Echogenic kidney (similar to spleen or liver)
ATN
Glomerulonephritis
Renal infiltration
Glycogne storage disease
Diabetes
Renal vein thrombosis
Leukemia
HIV
Kawaski disease
Loss of normal corticomedullary differentiation
Pylenephritis (focal nephronia)
Infantile polycystic kidney
Adult polycystic kidney
Medullary cystic kidney
late renal vein thrombosis
Medullary nephrocalcinosis
lasix
Hyperparathyoidism
RTA
Hypercalcemia or hypercalciruia (milk alkali, Idiopathic, sarcoidosis, hypervitaminosis D)
Oxalosis
Medullary sponge
Congenital ureteric obstruction
primary megaureter
ureterocele
distal uretal stenosis
Uretal atresia
Circumcaval ureter
Bladder diverticulum
Adrenal mass
Neonatal hemorrhage
Neruoblastoma
Rare: teratoma, adenoma, carcinoma, pheo
Other retro masses: wilms tumor, hydronephrotic upper pole, retroperitoneal adenopathy, hepatoblastoma, splenic mass
Cystic structure in or near bladder (US)
Bladder: hutch diverticulum, urachal remnant, normal bladder ears
Ureter: ectopic insertion of ureter, ureterocele, megaureter
Other: ovarian cyst, mesentaric, omental cyst
Large abdominal cystic mass
Lymphangioma (multiseptated)
Enteric duplication cyst (unilocular with bowel signiture)
Meconium pseudocyst (unilocular with echoes and debris)
Choledochal cyst
Adrenal hemorrhage
Ovarian cyst
Presacral mass
Rectal duplication
Anterior meningocele
Teratoma
Neuroblastoma
Interlabial mass
Ectopic ureterocele
Periurethral cysts
Rhabdomyosarcoma of vagina
prolapsed urethra
Imperforate hymen
Enlarged Head
Hydrocephalus
Subdural hematoma
Calvarial abn: benign macrocrainia, chodrodystrophies
Brain abn:Beckwith-wiedermann, hemiatrophy, cerebral gigantism
Small Head
Absent of atrophic brain
Crainiosynostosis
Shunt placement
Thick skull
Metabolic: healing stage of renalosteodystrophy, hyperparathyroidism, anemias (SSD ans thalasemia)
tumor: leukemia/lymphoma
Other: chronic decreased intracranial pressure(shunt), dilantin therapy, dysplasia (fibrous dysplasia engelmann's disease)
Lytic skull lesions
EG
Leukemia/lymphoma
Fibrous dysplasia
Dermoid/epidermoid
Hyperparathyroidism
Intracranial calcification
Physiologic
Choroid plexus calc
Habenula calc
Pineal gland calc
Falx: dura, pacchionian bodies calc
Hemangioblastoma calc
Intracranial calcification
Not physiologic
Tumor: Crainopharyngioma>oligodendroglioma> gliomas
Infection: TORCH
Congenital: atrophy or hypoplasia, TS, Sturge weber
Metabolic: idiopathic hypercalcemia, lead poisoning, hypoaparathyroidism, Fahr's disease
Trauma
Vascular: AVM, hematoma, aneurysm
Enlarge sella turcica
Tumor: craniopharyngioma, hypothalmic glioma, germ cell tumors, meningioma, pituitary adenoma
Increased intracranial pressure
Empty sella
nelson's disease
Commom Pediatric bone tumors
1: EG, Ewings sarcoma, OSA, Bone cysts ( UBC, ABC)
2: neuroblastoma mets, lymphoma, leukemia
With fluid-fluid level: ABC, telangiectatic OSA, GCT, single cyst with pathologic fracture
Widened joint space
Joint effusion: septic arthritis, hemarthrosis, transient toxic symovitis, JRA
Synovial thickening without articular cartilage destruction: JRA, Hemohiliac arthropathy
Bowed bones
Metabolic: Rickets
Dysplasia: neurofibromatosis, osteogenesis imperfecta, fibrous dysplasia
Diffuse Pediatric osteoenia
Rickets
Hyperparathyroidism
Immoblization
JRA
Uncommon: gangliosidosis, mucolipidosis, adult causes
Dense bones in children
Congenital: osteopetrosis, pyknodyostosis, melorheostosis, progressive diaphyseal dysplasia (engelmanns), infantil cortical hyperostosis, idopathic hypercalcemia of infacny (williams), generalized cortical hyperostosis (van buchem's), pachydermoperiostosis
Other: hypothyroidism, congeital syphilis, hypervitaminosis D
Symmetric periosteal rxn in children
Tumor: Neuroblastoma, leukemia,lymphoma
Infection: congenitalsyphiles or rubella
Metabolic: Hypervitaminosii A, D, Prostaglandin therapy, scurvy
Trauma: battered child syndrome
Vascular: bone infarctions
Mnemonic for periosteal rxn
SCALP
scurvy
Caffey's disease
Accident, hypervitaminosis A
Leukemia, lues
Physiological, prostaglandin inhibitors
Deformed epiphyisis
Acquired: avascular necrosis, LCP disease, steroids
Trauma: osteochondritis dissecans
Infection
Hypothyroidism
Congenital: multipla epiphyseal dysplasia, myer's dysplasi, morquios syndrome
Enlarged epiphysis
Hemophilia
JRA
Chronic infectious arthritits
Healed LCP disease
Epiphyseal dysplasia hemimelia
Tranverse metaphyseal lines
Lucent lines (undermineralization)
Neonates: stress lines d/t fever, CHD, any severe disease
>2 years: neuroblastoma, mets, lymphoma, leukemia
Transverse metaphyseal lines
Dense lines
Neonated: growth recovery lines
>2 years: heavy metal poisoning, healing rickets
Widened growth plate (>1mm)
Rickets
Salter Harris I
Tumor: lymphoma, leukemia, neuroblastoma
Infection: osteomyelitis
Metaphyseal fragments
Battered child
Trauma
Blounts disease
Ostoemyelitis
Vertebra Plana
localized platyspondyly
Mets-neuroblastoma
EG
Leukemia, lymphoma
infection
trauma
Generalized platyspondyly
osteogenesis imperfecta
dwarfism
Morquios
Cushings syndrome
Fused Vertebrae
Isolated fusion
Klippil-Feil syndrome (C2-3 fusion, torticollis, short neck)
Posttraumatic
Large vertebral body or abnormal shape
Blood dyscrasias (expansion of red marrow) sickle cell, tahlaasemia
Atlantoaxial subluxation
Downs
Morquio's
JRA
Trauma
Disk space narrowing
Common: infection, block vertebra, scheuermann's disease, severe kyphosis or scoliosis
Uncommon: congenital, Cockayne, Kniest dysplasia, morquios, spondyloepiphyseal dysplsia
Acquired: inflammatory arthritis (rheumatoid, AS), herniated disk, neuropathic (syrinx), trauma
Enlarged disk space
Osteoporsis
Biconcave vertebra
Gaucher's disease
Platyspondyly
Sickle cell disease
Trauma
Intervertebral disk space calcification
Common: idopathic, post traumatic
Uncommon: pinal fusion, ochronosis, aarskog syndrome, cockaynes syndrome, homocystinuria, hypercalcemia, hyperparathyroidism, hypervitaminosis D, infection, paraplegia, juvenile chronic arthritis
Pediatric sacral abnormalities
Meningocele
Neurofibromatosis
Presecral teratoma
Agenesis
Radial ray defiiciency
Holt-oram syndrome
Polands syndrome
Fanconi's anemia
Thrombocytopeniaabsent radius syndrome
Polydactyly
Familial polydactly
Chondroectodermal dysplasia (ellis van creveld)
Trisomy 13,14,15
Laurence-moon-bardet-biedel syndrome
Abnormal 4th metacarpal
Short: turner's, growth arees (sickle cell, infections)
Long: macrodystrophia lipomatosa, neurofibromatosis
Delayed bone age
Systemic: hypothroidism, cyanotic heart disease, chronic pulmonary disease
HGH defiency: isolated GH defiency, cranipharyngioma, infections
Peripheral tissue nonresponsiveness: African pygmies, Turner's syndrome, Consitutional short stature
Hemihypretrohpy
intraabdominal tumors ( wilms)
Arteriovenous fistula
Lymphangioma
Isolated anomaly
Williams syndrome
aortic stenosis
peripheral pulmonic stenosis, diffuse coarctation of abdominal aort and stenosis of visceral branches
Multisytem abnormalities: retardation, dentation, elfin facies
Beckwith-wiedmann syndrome
Macroglossia
Vsceromeglay
gigantism
Omphalocele
Wilms tumor
Premature infants
hyaline membrane disease
NEC
germinal matrix hemorrhage
Periventricular leukoencepathy
PDA