Fetal gastrointestinal/genitourinary with pathology registry review Flashcards

(46 cards)

1
Q

GI abnormalities

A

Most often result in polyhydramnios
-If GI obstruction/disturbance where fluid cannot be swallowed or absorbed normally, build up of fluid will take place
-Kidneys continue producing fluid even with GI obstruction

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2
Q

Stomach

A

Inferior to diaphragm
*should empty and fill every 30 mins

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3
Q

Fetal cord insert

A

Inferior to level of the kidneys, should be smooth with no herniations or mass

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4
Q

Bowel

A

Slightly more echogenic than liver

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5
Q

Esophageal atresia

A

Absence of a section of the esophagus
*associated with VACTERL and T18

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6
Q

Tracheoesophageal fistula

A

Esophagus and trachea form a connection

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7
Q

Sonographic appearance of esophageal atresia

A

No visualization of the stomach and polyhydramnios

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8
Q

Duodenal atresia

A

Fluid filled stomach and fluid filled proximal duodenum
-“double bubble”
-Polyhydramnios
*associated with T21

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9
Q

Anorectal atresia

A

Most common type of colonic atresia that leads to bowel obstruction

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10
Q

Sonographic appearance of anorectal atresia

A

Dilated loops of bowel
*look for VACTERL

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11
Q

Hirschsprung disease

A

Functional bowel obstruction caused by the absence of nerved within bowel wall

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12
Q

Sonographic appearance of hirshsprung disease

A

Dilated loops of bowel

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13
Q

Echogenic bowel

A

Bowel bright as bone
*associated with T21 and cystic fibrosis

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14
Q

Neuroblastoma

A

Adrenal gland tumor, mass superior to kidney
-MOST common malignant abdominal mass in neonates

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15
Q

Hepatomegaly

A

Most common abnormality of the liver
-Cause ac to be larger than expected GA
*associated with beckwith-wiedemann

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16
Q

Gastroschisis

A

-Herniation of bowel through an opening on RIGHT side of cord insertion
-Not covered by a membrane or skin
-Larger defects may include stomach and other abdominal organs
-Usually isolated finding
-Requires surgery
*ELEVATED AFP

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17
Q

Omphalocele

A

-Persistent herniation of bowel and possibly other organs into the BASE of the umbilical cord after 12 weeks
-Bowel and possibly liver
-ALWAYS midline and covered by membrane
-AFP possibly normal due to being covered by membrane
*STRONG association with T18, T13, pentalogy of cantrell

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18
Q

Fetal kidney formation

A

Form in pelvis and rise to renal fossa by week 9
*if doesn’t rise then = pelvic kidney

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19
Q

Fetal kidney functionality

A

-Fully functional at 10 weeks
-Produce urine at 12 weeks

20
Q

Fetal bladder

A

Seen by week 13 on US

21
Q

Fetal kidneys seen on US

22
Q

Amniotic fluid

A

Mostly made of fetal urine AFTER 16 weeks
-As long as one functioning kidney present, normal fluid levels present
*affected heavily by renal function

23
Q

Most common cause of oligohydramnios

A

Renal abnormalities

24
Q

Most common renal anomaly

A

Duplicate/double collecting system divided into upper and lower moiety/poles

25
Unilateral renal agenensis
-Failure of one kidney to form -Most common -Fluid and bladder will be normal since present kidney is functional
26
Bilateral renal agenesis
-Failure of BOTH kidneys to form -NO bladder and NO fluid *Potters syndrome
27
Sonographic signs of renal agenesis
-Adrenal gland is flattened and parallel to spine (usually on upper pole of kidney) -Absence of renal artery branches coming off the aorta in coronal view
28
Autosomal recessive polycystic kidney disease (ARPKD)
-Infantile -Bilateral enlarged, echogenic -NON functional = no fluid, no bladder -Associated with meckel-gruber -Oligo/anhydramnios *FATAL
29
Autosomal dominant polycystic disease (ADPKD)
-Adult version, doesn't affect until late adulthood -Bilateral enlarged, echogenic -FUNCTIONING -Normal bladder, normal fluid -Cyst develop as adults
30
Sonographic appearance for PKD
Bilaterally enlarged, echogenic kidneys. Cysts are not visualized (microscopic)= echogenic enlarged appearance
31
Multicystic dysplastic renal disease
Large cysts affecting entire kidney, kidney appears to fill entire abdomen -Affected kidney is NON functional -Unilateral = normal fluid/normal bladder -Bilateral= no fluid/ no bladder
32
Obstructive cystic dysplasia
Kidney becomes small and echogenic with peripheral renal cyst -Caused by early renal obstruction -Unilateral or bilateral -NON functional -Bilateral = oligohydramnios
33
Most common fetal abnormality
Hydronephrosis (AKA pelvocaliectasis, pelviectasis/pyelectasis, caliectasis -- depends on dilated area of kidney)
34
Urinary tract obstruction
Any obstruction to normal succession of urine flow will result in back up and cause dilation proximal to obstruction
35
Measurement of dilated pelvis
-In transverse and AP > 4mm in 2nd trimester = pyelectasis >7mm in 3rd trimester = pyelectasis
36
Location of ureteropelvic junction obstruction (UPJ)
Most common cause of hydro, pyelectasis only
37
Location of ureterovesicular junction obstruction (UVJ)
Least common cause of hydro, kidneys and ureter
38
Urethra obstruction
Bladder outlet obstruction, everything from bladder up is dilated
39
Bladder outlet obstruction/prune belly syndrome
Posterior urethral valve causes obstruction in male fetus -Massively dilated bladder -Key hole sign -Dilation of ureters and kidneys eventually occurs
40
Key hole sign in bladder
Dilated bladder (megacystis) and dilated posterior urethra
41
Triad of prune belly (eagle barret syndrome)
Absent abdominal musculature, undescended testis, urinary tract abnormalities
42
Bladder extrophy
Bladder located outside the pelvis, lower abdominal mass inferior to umbilicus -May be included with cloacal extropy and extropy of intestines and genitalia
43
Cloaca
Everything at the bottom including true pelvis genitalia
44
Clitoromegaly
Most common cause of ambiguous genitalia in females
45
Common causes of ambiguous genitalia in males
Micropenis, hypospadias, undescended testis
46
Hypospadias
Abnormal curvature of penis