Urinary System Quiz Flashcards

(40 cards)

1
Q

Urinary System Consists of:

A

Upper urinary tract & lower urinary tract (bladder and urethra).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Location and Number of each:

Kidneys
Ureters
Urinary bladder
Urethra

A
  • 2 Kidneys (upper)
  • 2 Ureters (upper)
  • Urinary bladder (lower)
  • Urethra (lower)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What can anomalies cause?

A

Anomalies can cause obstruction or stasis, create infections, impair renal function, and/or prompt stone formation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Are kidneys retroperitoneal?

A

yes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Which kidney sits lower than the other?

A

Right kidney sits lower than the left

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Which organs are vital for homeostasis?

A

Kidneys

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What do kidneys do?

A

detoxify the blood, maintain normal pH, iron, and salt levels in the blood.
also work to regulate blood pressure by producing the enzyme renin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is urine formed?

A

Urine is formed and excreted through filtration and reabsorption of blood which results in approximately 1-1.5L of urine per day

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is Nephron?

A

Functional unit of the kidney responsible for formation of urine (filtration). Bladder is the reservoir until excretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What Muscles are posterior and lateral to the kidneys?
know their locations

A

Psoas, Erector Spinae, Quadratus Lumborum, Latissimus Dorsi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

the process of urine formation in a nephron:

Step 1

A

The nephron’s cup-shaped Bowman’s Capsule surrounds a knot of blood capillaries called the glomerulus. Most of the blood filters into the glomerulus due to pressure from the circulatory system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Step 2

A

This fluid/blood is then passed through the nephron tubule, which has 4 main parts (proximal convoluted tubule, loop of Henle, distal convoluted tubule, and the collecting duct).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Step 3

A

In the proximal convoluted tubule, a considerable amount of reabsorption occurs. Small proteins, glucose, and ions are returned to the blood. About 75% of the filtrate is returned in this section of the nephron.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Step 4

A

In the loop of Henle - Salt is actively transported out of the filtrate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Step 5

A

In the distal convoluted tubule, urine is passed to the collecting duct where it is concentrated.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

and Lastly step 6

A

It then leaves the collecting duct into the pelvis of the kidney, which leads to the ureter and the bladder where it is stored.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Clinical Indications:

A

-Flank and/or back pain

-Signs or symptoms that may be referred from the kidney and/or bladder regions such as hematuria

-Abnormal laboratory values or abnormal findings on other imaging examinations suggestive of kidney and/or bladder pathology

-Follow-up of known or suspected abnormalities in the kidney and/or bladder

-Evaluation of suspected congenital abnormalities

-Abdominal trauma

18
Q

Kidney Protocol

A

Kid Long RT MED/LAT - Long sweep w images medial to lateral

Kid Long RT/LIVER - comparison (*LT = Kid Long LT/SPLEEN comparison)

Kid Trans RT S/I – Transverse sweep w images superior to inferior

*REPEAT on LT

19
Q

Renal Agenesis

A

Absence of kidney on one side (unilateral) large kidney on contralateral side.
Left kidney agenesis is more common. +Men. Bilateral agenesis often presents in utero with oligohydramnios and pulmonary hypoplasia, and is incompatible with life.

20
Q

Dromedary Hump

A

Local bulge of lateral border of the LEFT kidney

21
Q

Junctional Parenchymal Defect

A

Wedge-shaped hyperechoic defect, anterior, usually right.

22
Q

Hypertrophied Column of Bertin (HCB)

A

Layer of renal cortex is folded toward the center of kidney.

23
Q

Hypoplasia

A

Developed but small. Clinical significance depends on volume of output, hypertension generally accompanies this anomaly.

24
Q

Hyperplasia

A

Overdeveloped kidney (LARGE). Often associated with renal agenesis or hypoplasia of contralateral kidney.

25
Horseshoe Kidney
Most common fusion anomaly. Lower poles of the kidneys are joined across the midline by a band of soft tissue. +Men. Generally unimpaired – but if obstruction present, surgery possible
26
Crossed Ectopia
One kidney lies across the midline and is fused to the other kidney. Second most common fusion anomaly.
27
Ectopic Kidney
Having one kidney that is out of its normal position (from birth, failure to ascend).
28
Double Collecting System (aka Duplex Kidney)
Duplication of collecting system - may be complete (2 ureters) or incomplete (1 ureter).
29
Nephrolithiasis
Stones in the kidney. They are composed of calcium and salt. Kidneys are the second most common area for calculi in the body.
30
Causes of Nephrolithiasis
metabolic disorders (calcium), high calcium intake, and chronic UTI’s. Common in Men >30 years old.
31
Clinical Indications of Nephrolithiasis
acute back/flank pain that may radiate into the ipsilateral groin. Possible dysuria, hematuria, cloudy urine, fever, and/or chills.
32
Anatomical Image of Nephrolithiasis
Hyperechoic structure(s) with posterior shadowing.
33
Hydronephrosis
Obstructive disease of the urinary system – dilatation of calyces and renal pelvis with urine. Long term can cause atrophy and loss of renal function.
34
Cause of Hydronephrosis
calculus/stone
35
Symptoms of Hydronephrosis
flank pain and blood or pus in urine. May have abnormal labs if damage is present.
36
Autosomal Recessive Polycystic Kidney Disease (ARPKD)
Genetic condition, formation of innumerable tiny cysts. Four kinds: Perinatal, neonatal, infantile, and juvenile.
37
Symptoms of ARPKD
Portal hypertension (in severe cases), Renal insufficiency - shown via elevated BUN/Creatinine - decreased GFR.
38
Radiological Images of ARPKD
Enlarged echogenic kidneys. May see hepatic fibrosis and splenomegaly in severe cases
39
Symptoms of ADPKD
Chronic UTI’s, Stone Formation, Back Pain, Headache, Increasing Abdomen Size, High blood pressure, Renal Insufficiency. (50% diagnosed with renal hypertension) (50% will need dialysis or transplant due to renal failure). Increased Bun & Creatinine, Decreased GFR.
40
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
More common than ARPKD. Bilateral renal enlargement is due to the formation of many cysts of various sizes. The cysts gradually enlarge as the patient ages. Over time cysts will compress and destroy normal tissue.