Fetal Genitourinary system Flashcards

1
Q
  • Originate in pelvis and migrate superiorly
  • Identified as early as 12-14 weeks
  • Small amount of fluid in renal pelvis=normal finding
  • AP renal pelvis ≥ 10mm is abnormal
  • 2 renal arteries = rules out agenesis
A

Kidneys

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2
Q

Congenital absence of one or both kidneys

A

Renal agencies

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3
Q

Very common, occurring in 1:1000 births

A

Unilateral

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4
Q

Potters Syndrome
• Bilateral renal agenesis (BRA)
• Pulmonary HYPOplasia
• Facial Anomalies & small for dates
• Associated w/ other chromosomal abn, Cardio, Gastro, Skeletal, genitourinary
• S/S: OLIGO, non distended bladder “lying down adrenal glands”

A

Bilateral

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5
Q
  • Inherited disorder w/ BILATERAL renal cysts
  • Kidneys will fail
  • S/S: Large echogenic kidneys
A

Polycystic kidney disease

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6
Q

• Collecting tubules are blocked…forming cysts up to 6cm in size.
• MCDK- usually UNI but can be BILATERAL
• S/S: Multiple peripheral cysts w/ possible OLIGO
** Solid Renal masses are rare but u must try to find origin- Kidney vs. Adrenal

A

Multicystic Dysplastic kidney

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7
Q
  • malignant tumor in adrenal gland, appears as echogenic suprarenal mass
A

Nueroblastoma

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8
Q

LOWERPOLES are fused, assoc w/ genetic syndromes.

A

Horseshoe kidney

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9
Q
  • MC cause of neonatal hydronephrosis
  • Congenital obstruction of urine from renal pelvis to ureter
  • S/S: Dilated renal pelvis, possible OLIGO
A

Uteropelvic Junction Obstruction (UPJ)

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10
Q

• LEAST common cause of hydro
• Occurs @ 3 levels
1. Ureteral duplication w/ ectopic ureterocele
▪ Duplicate ureter in upper pole enters bladder abn location causing ureterocele
2. Congenital/Obstructive megaloureter
3. UVJ stenosis
*****Ureterocele round cyst-like structure within the bladder

A

Ureterovesical Obstruction (UVJ)

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11
Q

• M/C in male fetuses

A

Bladder outlet obstructions

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12
Q

(PUV) Congenital folds of urethra act as valves and obstruct flow
▪ Can cause damage to kidneys, ureter and bladder
▪ S/S: “KEY HOLE” appearance of bladder, bilateral hydro and OLIGO

A

Posterior urethra valves

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13
Q

Complete obstruction not compatible with life

A

Ureteral atresia

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14
Q

rare malformation where gastrointestinal and genitourinary tracts combine
single opening to perineum becomes obstructers and has poor prognosis `

A

Cloacal malformation

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15
Q

dilated urinary bladder cases atrophy of abdominal wall

  • most common cause is posterior uretherl valve
  • associated with pulmonary hypoplasia & OLIGO
A

prune belly syndrome

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