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58 Cards in this Set

  • Front
  • Back
what is it
what is it
circumvallate: abnormal shape to placenta, marginal fold of the chorion and projection of villous tissue beyound endge of chorion plate, valley between membranes and fetal surface of placenta
what is it
what is it
accessory, or succenturiate, lobe of the placenta, promotes bleeding
placenta
placenta
for review - no fold to membranes in circummarginate
what is it
what is it
false knot
placenta
placenta
amnion nodusum: associated with oligohydramnios
placenta
placenta
amnion nodusum: associated with oligohydramnios
placenta
placenta
squamous metaplasia - can look like amnion nodosum
placenta
placenta
acute chorioamnionitis
placenta
placenta
listeria - can see intervillous abscesses microscopically
acute villitis - what bugs
e coli, GBS
chronic active villitis - bugs (5)
non-syphylitic spirochetes, GNRs, Rickettsiae, HSV, VZV
placenta
placenta
meconium - patchy infiltrates on CXR (chemical pneumonitis) slimy and brown
on micro: amnion starts to degenerate, then you know it's real; can get skin and nail discoloration on child
placenta
placenta
for review
subamniotic hematoma - no consequence
chronic subchorionic plaques - no consequence

look in decidua for pre-eclampsia (decrease blood flow with placental infarcts, maternal atherosis- vacuolated and degeneration and smooth muscle persistence - after 29 weeks)
placenta
placenta
hematoma (intraparenchymal) - from fetal blood, in between villi
placenta
placenta
abruptio - indentation of placenta
placenta
placenta
CMV - torch
placenta
maternal floor infarction (massive perivillous fibrinoid deposition)
twins
twins
for review
monozygotic but divides <3 days dichorionic, diamniotic
monozygotic splits 3-8 days monochorionic, diamnionitic
>8 days monochorionic monoamnionitic (50% mortality)
if monochorionic - look for anatomoses, know you have a monozygotic twin
twin type
twin type
monozygotic
placenta
placenta
chorioma
placenta
placenta
chorioangiosis - criteria: >10 villi in clusters containing >10 capillaries per villus; associated with placenta hypoxia (see in Andes)
placenta
placenta
partial mole - one maternal, two paternal, can have fetal parts; dimorphic villi; trophoblastic inclusions
what is it
what is it
spina bifida - malformation; myelomenigocele
what is it
what is it
amniotic bands - disruption - amnion is sticky
what is it
what is it
deformation, club foot
what is it
what is it
potter sequence (sequence is group of abnormalities which occurred due to single condition)
fx include: oligohydramnios, low set ears, depressed nasal buds, club foot, contractures
b/c renal malformaiton - oligohydramnios- etc.
what syndrome: exophthalmos, macroglossia, giantism, craniofacial abnormalities, microcephaly, hemihypertrophy, omphalocele, neonatal hypoglycemia, organomegaly, cytomegaly of adrenal cortex, islet cell pancreas, predisposition to malignant tumors
beckwith-wiedemann
what syndrome
what syndrome
beckwith-wiedemann***
exophthalmos, macroglossia, giantism, craniofacial abnormalities, microcephaly, hemihypertrophy, omphalocele, neonatal hypoglycemia, organomegaly, cytomegaly of adrenal cortex, islet cell pancreas, predisposition to malignant tumors
cytogenetic abnormalities in beckwith-wiedemann
dysregulation of imprinted genes in 11p15
maligancies for which beckwith-wiedemann syndrome is associated
wilms, adrenocortical ca, hepatoblastoma, gonadoblastoma, brain stem glioma
what syndrome
what syndrome
alagille - AD, liver, heart and kidney affected
facial - recessive, saddle nose
what syndrome
what syndrome
patau, czome 13 (trisomy)
Palate (cleft), Proboscis, Punched out scalp, low set ears, polydactyl

four ps and and e
what syndrome
what syndrome
edwards, 18, rocker bottom feet, barrel chest, low set ears with pointed upper helix
sx of cri du chat
small for gestational age
laryngeal hypoplasia
MR
hypotonia
del 5p
sx of klinefelters
sx of klinefelters
for review - tall, aractodactyl
what is it
what is it, where found
cystic hygroma in turners
most common abnormalities in embryo
Neural tube
Cleft lip
Limb defects
fetal defects (just read)
Neural tube defects (spina bifida)
Amnion Rupture Sequence (amniotic bands)
Cervical Cystic Hygromas (turners)
Omphalocele (b-w syndrome)
Genitourinary *
Hydrops Fetalis (ABO incompatibility, etc)
Contractures and Pterygia
Cleft Lip and Palate (patau)
Congenital Heart Defects *
two common czomal abnormalities for CHD
22q11 and trisomy 21
what is it, what associated with
what is it, what associated with
coarctation aorta, turners, can survive a couple of days before closure of PDA if in right spot
what is it
what is it
tetralogy of fallot - anterior displacement of infundibular septum;
pulmonary infundibular stenosis (outflow obstruction)
overriding aorta
VSD
RV hypertrophy
if fifth - ASD
common factors causing asymmetric IUGR
Toxemia, chronic hypertension, narcotics,
alcohol, cigarettes, antimetabolite rx.,
dilantin
common birth trauma factors
Clavicular fracture, brachial plexus injury, etc.
Intracranial hemorrhage
Tear in falx, tentorium, or brain substance
squamous metaplasia vs
aminion nodusum
sm - insertion site
an - peripheral and picks off easily
maternal arteriole in decidua
loses smooth muscle
leading up to funitis (which one first)
vein before arteries (2)
candida in placenta
microabscesses on umbilical cord
associations: fetal thrombotic arteriopathy in placenta
protein c and s deficiency; thrombus in chorionic plate vessels and avascular villi - problem with fetal circulation
hemorrhage endovasculosis; venous stasis
problem in umbilical cord; hemorrhage in villi
chronic villitis
TORCH
placental malaria (granular pigment between villi)
recurrent pregnancy loss 3 causes
chronic villitis of unknown etiology (GVD-like)
massive chronic intervillitis - mononuclear infiltrate
maternal floor "infarction" - exaggerated perivillous fibrin
smith-lenle-opis
defect in cholesterol synthesis
prune belly syndrome
pcos?
lack of abdominal wall muscles
type of chd commonly found in trisomy 21
endocardial cushion defects
common associated with CHD, czomal d/o
e.g. del 22
single umbilical artery most commonly associated with
CHD
most common CHD (top 5)
tetrology of fallot
transposition of great arteries
coarctation of aorta
vsd
pda
VSD where most occur
most common - membranous