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DMS 281 OB Pathology Review
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what is prune belly syndrome
agenesis of the abdominal wall musculature causing severe distention (greater than PUV)
what is urethral atresia
bladder distention in FEMALES
who and what is the key hole appearance associated with
males ONLY and PUV (posterior urethral valve obstruction)
what is UVJ associated with
dilated renal pelvis AND ureter (megaureter)
what is the most common reason for hydronephrosis
UPJ obstruction
what is the most common fetal anomaly
hydronephrosis
what measurement indicates hydronephrosis
>7mm AP dimension after 28 weeks
how would adult polycystic kidney disease appear on ultrasound (OB)
kidneys typically appear normal in utero and neonatal, with manifestation not occurring until 3rd or 4th decade of adulthood
how would multicystic dysplastic kidney disease appear on ultrasound
unilateral (usually BUT can be bilateral), renal tissue displaced by various sized cysts normal fluid level... IF BILATERAL: oligohydramnios and fatal
how would infantile polycystic kidney disease appear on ultrasound
bilaterally enlarged echogenic kidneys after 24 weeks, NO visible cysts, oligohydramnios, and may not be able to see bladder
TRUE OR FALSE: infantile polycystic kidney disease is always bilateral
TRUE
bilateral renal agenesis may result in:
severe oligohydramnios, small thorax, pulmonary hypoplasia, dolicocephaly
in unilateral renal agenesis, what will the size of remaining kidney most likely be
the size of the signl kidney may be larger to compensate
what is hydrops
collection of fluid in 2 or more spaces
what is meconium ileus
dilated bowel loops containing thick meconium (poop)
what is meconium ileus associated with
cystic fibrosis
what is hirschsprung's disease
innervation of the large intestine resulting in megacolon
which condition is duodenal atresia associated with
trisomy 21
what is duodenal atresia
malformation of the duodenum creating an obstruction of the passage of amniotic fluid
which condition is associated with the double bubble sign
duodenal atresia
what is a cleft palate associated with
small stomach and/or polyhydramnios from not swallowing amniotic fluid
when should suspicion for esophageal atresia arise
when the stomach is persistently not seen after 19 weeks (should be seen around 14-15 weeks)
what is the most common type of esophageal etresia
distal tracheoesophageal fistula
what is beckwith-weidemann syndrome characterized by
large organs
what is amniotic band syndrome
rupture of the amnion allowing fetal anatomy to become entrapped to the sticky chorion
what can amniotic band syndrome lead to
malformations and amputations of limbs
what is pentalogy of cantrell almost always associated with
limb reduction anomalies
what are the five anomalies of pentalogy of cantrell
omphalocele & ectopic heart (most common 2), defect in the lower sternum, anterior diaphragm, and diaphragmatic pericardium
what is useful when imaging hypospadius
color Doppler to look for urine flow
what is hypospadius
an abnormal opening of the penis on the under side rather than at the tip
what is gastroschisis
an opening typically to the right of the umbilical cord insertion in the layers of the abdominal wall allowing protrusion of the intestines, no covering!!!
what is an omphalocele
weakness of the abdominal musculature & skin resulting in a herniation of the abdominal contents into the base of the umbilical cord, covered by a membrane
which type of CCAM has a more favorable outcome
type 1 (large dominant cyst 3-10cm replaces lung tissue)
what is CCAM
abnormal overgrowth of bronchial tissue and lack of normal alveoli, typically in the lower lobes, there are 3 types
what does CCAM stand for
cystic adenomatoid malformation
what is BPS
a mass of nonfunctioning lung tissue that does not communicate with the bronchial tree, has a feeder vessel so color Doppler is important
what does BPS stand for
bronchopulmonary sequestration
what is a typical cause of pulmonary hypoplasia
oligohydramnios
what is a reduction in lung volume
pulmonary hypoplasia
what type of hydrocephalus is due to obstruction within the ventricular system often between the 3rd and 4th ventricle (stenosis of the aqueduct of sylvius)
non-communicating hydrocephalus
which type of hydrocephalus is due to overproduction OR under absorption of CSF
communicating hydrocephalus
what ventricle measurement is considered ventriculomegaly
dilation >10 mm (1cm)
what is a theorized cause of hydranencephaly
results from insult or bilateral occlusion of the fetal internal arteries OR from congenital infection
which condition involves a fluid filled head replacing the cerebral hemispheres
hydranencephaly
which condition results in 1 common large monoventricle and has 3 forms
holoprosencephaly
what is associated with the absence or abnormally shaped CSP
agenesis of corpus collosum
what is Arnold Chiari associated with
spina bifida
what is downward displacement of the 4th ventricle into the cervical canal resulting in an obliterated/small cisterna magna measurement and banana shaped cerebellum
Arnold Chiari Malformation
which condition involves a large 4th ventricle cyst seen in the posterior fossa replacing the cerebellum due to agenesis of the vermis, increases the cisterna magna measurement, and results in hydrocephalus of 3rd & lateral ventricles
Dandy Walker Malformation
which condition is associated with frog-like bulging eyes
anenecephaly
what is more common: anencephaly or acrania?
anencephaly is the most common neural tube defect whereas acrania is very rare
how is anencephaly different from acrania
anencephaly is the absence of the skull AND brain tissue (brain stem still present) whereas acrania is the absence of the skull WITH presence of brain tissue
what is a cystic hygroma associated with
Turner's Syndrome
what is a collection of lymphatic fluid typically located at the back of the neck due to obstruction of lymphatic channels
cystic hygroma
what is a proboscis associated with
holoprosencephaly
what is a soft tissue structure extending from the front of the face called
proboscis
which condition is associated with Beckwith-Wiedemann Syndrome
macroglossia
which condition is associated with Pierre-Robin Syndrome?
micrognathia
which condition is associated with an abnormally large head, 2-3 standard deviations above normal
macrocephaly
what is a known cause of microcephaly
zika virus
which condition is associated with an abnormally small head, 2-3 standard deviations below normal?
microcephaly