Urinary System Flashcards

1
Q

The urogenital system develops from what type of tissue?

During lateral folding, what ridges appear?

A
  • intermediate mesenchyme (dorsal body wall of embryo)
  • urogenital ridge (each side of dorsal aorta)
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2
Q

The nephrogenic cord will give rise to the …?

The gonadal ridge will give rise to the …?

A

nephrogenic cord = urinary system

gonadal ridge= genital system

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3
Q

What are the 3 sets of kidneys?

Which sets are functional and which are permenent?

A

pronephroi (never functional; appear@ week 4)

mesonephroi (appear@ week 4; functions briefly for 4 weeks)

metanephroi (begin developing@week 5; permanent kidney @ week 10);S1-S2

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4
Q

What persists after the pronephri degenerates?

What does this become?

A

pronepheric ducts persist

  • becomes the **Wolffian duct **(mesonephric duct)
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5
Q

The mesonephric ducts open into what structure?

The mesonephroi degenerate at the end of the first trimester, their tubules become what adult structure?

A
  • the cloaca (trigone of urinary bladder)
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6
Q

The primordia of permanent kidneys starts developing at what week?

They are functional by what week?

A
  • week 5

- week 8 (mesonephroi)

* urine is secreted into amniotic cavity

* fatus swallows 100s mL of amniotic fluid/day

*fetal waste eliminated by maternal kidneys

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7
Q

By what week are the kidneys in their final abdominal position?

  • what rotational change in position takes place?
A

week 9 (become fixed to suprarenal glands)

  • 90 degrees medially; hilum faces medially

(kidneys eventually become retroperitoneal)

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8
Q

How does the blood supply change in the ascending kidney?

How many different positions does it have?

A

renal arteries:

1st: branches of common iliac arteries
2nd: distal end of the aorta
3rd: new branches from aorta

(3 positions in total)

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9
Q

Accessory Renal Arteries

(Supernumerary renal arteries)

A
  • about 25% of adult kidneys have two to four renal arteries
  • usually arise from the aorta
  • accessory renal artery to inferior pole of kidney may cross anterior to

ureter + obstruct it = hydronephrosis (distension of renal pelvis + calices with urine)

  • if accessory artery is damaged/ligated kidney part supplied = ischemic
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10
Q

Unilateral Renal Agenesis

A
  • left kidney is usually absent
  • usually asymptomatic (other kidney = compensatory hypertrophy)
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11
Q

Bilateral Renal Agenesis

A

failure in development of the metanephric diverticula

- oligohydramnios (b/c little/no urine excreted into amniotic cavity)

  • incompatible with postnatal life b/c associated pulmonary hypoplasia**
  • ** new developments = potential survival with dialysis & early kidney transplant*

Characteristic facial appearance:

  • eyes widely separated
  • epicanthic folds (wrinkly skin)
  • ears are low-set
  • broad nose and flat
  • limb defects (lack of space to develop)
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12
Q

Ectopic Kidney

A

One or both kidneys in abnormal position

failure to alter position during embryo growth

  • in pelvis (pelvic kidney) or inferior part of the abdomen (lumbar kidney)

most common = pelvic

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13
Q

Horseshoe Kidney

A

poles of kidneys are fused; (usually inferior poles)

  • lies in the hypogastrium, anterior to the inferior lumbar vertebrae
  • usually asymptomatic
  • normal ascent is prevented b/c they are caught by the root of inferior mesenteric artery
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14
Q

Ureteropelvic Junction Obstruction (UPJ)

A

obstruction to urine flow from the renal pelvis to the proximal ureter

_**most common congenital obstruction of the urinary tract**_

  • severe uteropelvic atresia => multicystic dysplastic kidney with severely dilated calyces
  • kidney consists of grapelike, smooth-walled cysts of variable size; b/t cysts are dysplastic glomeruli + atrophic tubules
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15
Q

Childhood polycystic kidney disease (PCKD)

A
  • kidneys are huge + spongy and contain cysts caused by dilatation of collecting ducts + tubules that compromise kidney function
  • autosomal recessive disease (short arm of chromosome 6 (p6))
  • associated clinically w cysts of the liver, pancreas, + lungs
  • treatment: dialysis + kidney transplant
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16
Q

Wilms’ Tumor (WT)

A

_**most common renal malignancy of childhood**_

  • large, solitary, well-circumscribed mass; (on cut) soft, homogeneous, + tan-gray
  • recapitulates different stages of embryologic formation of kidney:

= 3 histologic areas: stromal, blastemal (tightly packed embryonic cells), tubular

17
Q

Duplications of the Urinary Tract

A

Cause: division of the metanephric diverticulum

  • degree of duplication depends on how extent the division was
  • Complete division = double kidney with bifid ureter or separate ureters

* supranumeracy kidneys*

18
Q

Ectopic Ureter

A

males: open into neck of bladder or into prostatic part of urethra

  • above external urethral sphincter = incontinence NOT common

females: open into bladder neck, urethra, vagina or vestibule of the vagina

  • below external urethral sphincter = incontinence IS common
19
Q

Ureterocele

(Simple vs. Ectopic)

A

simple ureterocele:

- distal end of ureter has cystlike protrusion into the submucosal layer of the urinary bladder

ectopic ureterocele:

  • cystlike protrusion into the submucosal layer of the urinary bladder associated with ectopic ureter + duplication
  • -* ureterocele is at the end of ureter from upper renal segment & is located inferior to other ureter opening
20
Q

What divides the cloaca into the urogenital sinus and rectal sinus?

How is the urogenital sinus further divided?

A

urorectal septum

urogenital sinus:

  • cranial vesicle = bladder
  • middle pelvic part = prostatic urethra (M)/ entire urethra (F)
  • caudal phallic part = primordium of penis or clitoris
21
Q

What are the tissue origins of the bladders layers?

What are the tissue origins of the Male & Female urethras?

A

BLADDER:

(M/F) epithelium = endoderm (vesicle part of urogenital sinus)

(M/F) other layers of its walls = splanchnic mesenchyme

URETHRA:

(most of M/ all of F) epithelium = endoderm (vesicle part of urogenital sinus)

(M/F) connective tissue + smooth m. = splanchnic mesenchyme

22
Q

How does the allentois contribute to the development of the bladder?

A
  • originally allentois is continuous with bladder
  • allentois constricts = urachus
  • urachas extendes from umbilicus –> apex of bladder
  • in adult, urachus = median umbilical ligament
  • (failure of urachus to constrict = urachal cyst or fistula)*
23
Q

Urachal cysts

A
  • originate from remnants of the epithelial lining of the urachus
  • NO connection b/t bladder & umbilicus
24
Q

Urachal Sinus

A

persistent inferior end of the urachus that dilates and opens into the bladder

25
Q

Urachal fistula

A

entire urachus remains patent , allowing urine to escape from its umbilical orifice

26
Q

Congenital Megacystis

A
  • large urinary bladder, may result from congenital disorder of the metanephric diverticulum; may associate w dilation of the renal pelvis

= absolute renal failure + **pulmonary hypoplasia; **lethal unless intrauterine treatment is performed

27
Q

Exstrophy of Bladder

A

- exposure + protrusion of mucosal posterior wall of bladder

- due to abdominal wall + anterior bladder wall failure

  • trigone of bladder + ureteric orifices are exposed
  • some cases = penis is divided in two parts
28
Q

Development of the Female Urethra:

A
  • lower portion of the urogenital sinus (endoderm)
  • develops endodermal outgrowths into surrounding mesoderm = urethral glands + paraurethral glands of Skene (homologous to prostate gland)
  • vestibule of vagina develops endodermal outgrowths = lesser and greater vestibular glands of Bartholin
29
Q

Development of the Male Urethra:

A
  • prostatic urethra, membranous urethra, bulbous urethra + proximal part of penile urethra = from lower portion of urogenital sinus (endoderm)
  • distal part of urethra (in glans of penis) = solid cord of ectodermal cells growing inward from tip of glans; joins rest of spongy urethra
30
Q

Development of the Suprarenal Glands:

A

cortex = mesenchyme; medulla = neural crest cells

- neural crest cells differentiate into chromaffin cells (stain yellow-brown)

- Week 6: cortex begins as aggregation of mesenchymal cells on each side of the embryo b/t root of dorsal mesentery + gonad

  • Cortex = very large during fetal period + at birth; grows smaller after birth
  • Cortex produces steroid precursors used by placenta for synthesis of estrogen

- At Birth = cortex + medulla (zona fasciculata + zona glomerulosa)

- End of year 3 = zona reticularis is visable

31
Q

Neuroblastoma (NB)

A
  • common extracranial neoplasm containing primitive neuroblasts (neural crest origin)
  • presents in children; found in extra-adrenal (60%) or within the adrenal medulla (40%)
  • metastasizes to bone marrow, bone, + lymph nodes.
  • -* common lab finding = increased urine vanillylmandelic acid (VMA) + metanephrine levels
32
Q

Pheochromocytoma (PH)

A
  • rare neoplasm; contains both epinephrine + norepinephrine
  • present in adults 40-60 years old; generally found in region of adrenal gland; may be found in extrasuprarenal sites
  • associated w persistent or paroxysmal hypertension, anxiety, tremor, profuse sweating, pallor, chest pain, and abdominal pain

- lab findings = increased urine vanillylmandelic acid (VMA) + metanephrine levels, inability to suppress catecholamines with clonidine, + hyperglycemia

  • Treatment: surgery or phenoxybenzamine (an a-adrenergic antagonist)
33
Q

Congenital Adrenal Hyperplasia (CAH)

(Female pseudointersexuality)

A
  • most common cause = mutations in genes for enzymes involved in adrenocortical steroid biosynthesis
  • excessive androgen production by suprarenal cortex = masculinization in females
  • Female pseudointersexuality = mild clitoral enlargement, complete labioscrotal fusion w a phalloid organ, or macrogenitosomia (in the male fetus)
  • cannot synthesized aldosterone = hyponatremia (“salt-wasting”), dehydration + hyperkalemia (hgh K+ levels)
  • Treatment = infusion of intravenous saline + long-term steroid hormone replacement (cortisol + mineral-corticoids)