Chapter 1: Evaluation of the urologic patient: History, physical examination, laboratory tests, imaging, and hematuria workup Flashcards

1
Q

Table 1.1
What are the 8 main components of the International Prostate Symptom Score (IPSS)?

A
  1. Incomplete Emptying
  2. Frequency
  3. Intermittency
  4. Urgency
  5. Weak Stream
  6. Straining
  7. Nocturia
  8. Quality of Life due to Urinary Symptoms
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2
Q

Table 1.1
What are the columns of the IPSS in terms of quantity?

A

Not at all
< 1 time in 5
Less than half the time
About half the time
More than half the time
Almost always

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3
Q

Table 1.1
How is nocturia graded on the IPSS?

A

None
1
2
3
4
=>5

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4
Q

Table 1.1
How is quality of life graded on the IPSS?

A

Delighted
Pleased
Mostly satisfied
Mixed-about equally satisfied and dissatisfied
Mostly dissatisfied
Unhappy
Terrible

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5
Q

Table 1.1
What is the question for Incomplete Emptying?

A

Over the past month, how often have you had a sensation of not emptying your bladder completely after you finished urinating?

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6
Q

Table 1.1
What is the question for Frequency?

A

Over the past month, how often have you had to urinate again less than 2 hours after you finished urinating?

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7
Q

Table 1.1
What is the question for Intermittency?

A

Over the past month, how often have you found you stopped and started again several times when you urinated?

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8
Q

Table 1.1
What is the question for Urgency?

A

Over the past month, how often have you found it difficult to postpone urination?

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9
Q

Table 1.1
What is the question for Weak Stream?

A

Over the past month, how often have you had a weak urinary stream?

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10
Q

Table 1.1
What is the question for Straining?

A

Over the past month, how often have you had to push or strain to begin urination?

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11
Q

Table 1.1
What is the question for nocturia?

A

Over the past month, how many times did you most typically get up to urinate from the time you went to bed at night until the time you got up in the morning?

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12
Q

Table 1.1
What is the question for quality of life?

A

If you were to spend the rest of your life with your urinary condition just the way it is now, how would you feel about that?

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13
Q

Memorize the 7 symptoms by creating a mnemonic sentence:

Incomplete Emptying (I)
Frequency (F)
Intermittency (I)
Urgency (U)
Weak Stream (W)
Straining (S)
Nocturia (N)

A

“I Feel It’s Urgent With Some Nocturnal trips.”

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14
Q

For the symptom frequency categories, remember the sequence 0-5:

A

Not at all (0)
Less than 1 time in 5 (1)
Less than half the time (2)
About half the time (3)
More than half the time (4)
Almost always (5)

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15
Q

For Nocturia, remember the sequence 0-5 with an additional category “None”:

A

None (0)
1 time (1)
2 times (2)
3 times (3)
4 times (4)
≥5 times (5)

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16
Q

For the quality of life due to urinary symptoms, memorize the 7 categories:

A

Delighted (0)
Pleased (1)
Mostly satisfied (2)
Mixed (3)
Mostly dissatisfied (4)
Unhappy (5)
Terrible (6)

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17
Q

Decreased libido
“Hippo Has Low Libido”

A

Antihypertensives: H
Hydrochlorothiazide: H

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18
Q

Erectile dysfunction
Mnemonic: “Pandas Prefer Ben’s Dysfunction”

A

Psychotropic drugs: P
Propranolol: P
Benzodiazepines: B

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19
Q

Ejaculatory dysfunction

Mnemonic: “Alligator Ponders Time Machine, Phenomenal Ants”

A

α-Adrenergic antagonists: A
Prazosin: P
Tamsulosin: T
α-Methyldopa: M
Psychotropic drugs: P
Phenothiazines: Ph
Antidepressants: A

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20
Q

Priapism

Mnemonic: “Aphrodite Has Thunderous Permanent Happiness”

A

Antipsychotics: A
Phenothiazines: Ph
Antidepressants: A
Trazodone: T
Antihypertensives: A
Hydralazine: H
Prazosin: P

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21
Q

Decreased spermatogenesis

Mnemonic: “Cats And Dogs Make Noisy Parties”

A

Chemotherapeutic agents: C
Alkylating agents: A
Drugs with abuse potential: D
Marijuana: M
Alcohol: A
Nicotine: N
Drugs affecting endocrine function: D
Antiandrogens: A
Prostaglandins: P

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22
Q

Incontinence or impaired voiding

Mnemonic: “Dancing Hippos Visit Overflowing Sinks”

A

Direct smooth muscle stimulants: D
Histamine: H
Vasopressin: V
Others: O
Furosemide: F
Valproic acid: V
Smooth muscle relaxants: S
Diazepam: D
Striated muscle relaxants: S
Baclofen: B

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23
Q

Urinary retention or obstructive voiding symptoms

Mnemonic: “An Odd Dolphin Flies, Catching Noisy Clouds, Laughing Alpha Llamas Dance”

A

Anticholinergic agents or musculotropic relaxants: A
Oxybutynin: O
Diazepam: D
Flavoxate: F
Calcium channel blockers: C
Nifedipine: N
Antiparkinsonian drugs: A
Carbidopa: C
Levodopa: L
α-Adrenergic agonists: α
Pseudoephedrine: P
Phenylephrine: Ph
Antihistamines: A
Loratadine: L
Diphenhydramine: D

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24
Q

Acute renal failure

“A Penguin Climbs An Amphitheater, Crying Out Near Pharaohs”

A

Antimicrobials: A
Aminoglycosides: A
Penicillins: P
Cephalosporins: C
Amphotericin: A
Chemotherapeutic drugs: C
Cisplatin: C
Others: O
Nonsteroidal anti-inflammatory drugs: N
Phenytoin: P

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25
Q

Gynecomastia

Mnemonic: “A Vivacious Camel Dances, Giggling Crows Mock Pheasants, Tricycles Aim Inward”

A

Antihypertensives: A
Verapamil: V
Cardiac drugs: C
Digoxin: D
Gastrointestinal drugs: G
Cimetidine: C
Metoclopramide: M
Psychotropic drugs: P
Phenothiazines: Ph
Tricyclic antidepressants: T
Amitriptyline: A
Imipramine: I

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26
Q
A

FIG. 1.1 Bimanual examination of the kidney.

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27
Q
A

FIG. 1.2 Examination of the inguinal canal.

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28
Q

Colorless: VOD

Imagine a glass of clear water.

A

(Very dilute urine, Overhydration)

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29
Q

Cloudy/milky: PPC

Picture a glass of milk.

A

(Phosphaturia, Pyuria, Chyluria)

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30
Q

Red: HHAAPP

Visualize a glass of red wine.

A

(Hematuria, Hemoglobinuria/myoglobinuria, Anthocyanin, Chronic lead and mercury poisoning, Phenolphthalein, Phenothiazines)

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31
Q

Orange: DPS

Think of a glass of orange juice.

A

(Dehydration, Phenazopyridine, Sulfasalazine)

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32
Q

Yellow: NRP

Envision a glass of lemonade.

A

(Normal, Phenacetin, Riboflavin)

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33
Q

Green-blue: BIAAMMMPRT

Imagine a glass of green smoothie.

A

Biliverdin, Indicanuria, Amitriptyline, Indigo carmine, Methylene blue, Phenols, Resorcinol, Triamterene

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34
Q

Brown: UPAACFMN

Picture a glass of iced coffee.

A

(Urobilinogen, Porphyria, Aloe, Chloroquine and primaquine, Furazolidone, Metronidazole, Nitrofurantoin)

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35
Q

Brown-black: AHMTCCMMMS

Visualize a glass of dark soda.

A

(Alcaptonuria, Hemorrhage, Melanin, Tyrosinosis, Cascara, Methocarbamol, Methyldopa, Sorbitol)

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36
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS
IgA nephropathy (Berger disease)

A

30

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37
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Mesangioproliferative GN

A

14

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38
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Focal segmental proliferative GN

A

13

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39
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Familial nephritis (e.g., Alport syndrome)

A

11

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40
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Membranous GN

A

7

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41
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Mesangiocapillary GN

A

6

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42
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Focal segmental sclerosis

A

4

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43
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Unclassifiable

A

4

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44
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Systemic lupus erythematosus

A

3

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45
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Postinfectious GN

A

2

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46
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Subacute bacterial endocarditis

A

2

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47
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Others

A

4

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48
Q

Glomerular Disorders in Patients With Glomerular Hematuria
DISORDER PATIENTS

Focal segmental disorders

A

Focal segmental proliferative GN (13 patients) and Focal segmental sclerosis (4 patients)

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49
Q

Top 3 most common glomerular disorders in patients with glomerular hematuria

A

“1. IgA nephropathy (Berger disease) - 30 patients, 2. Mesangioproliferative GN - 14 patients, 3. Focal segmental proliferative GN - 13 patients”

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50
Q

“Least common glomerular disorders in patients with glomerular hematuria”

A

“Systemic lupus erythematosus (3 patients), Postinfectious GN (2 patients), Subacute bacterial endocarditis (2 patients)”

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51
Q

What is glomerular hematuria?

A

Glomerular hematuria refers to the presence of blood in the urine that originates from the glomeruli, which are tiny, specialized structures in the kidneys. The primary function of glomeruli is to filter blood and form the initial filtrate that eventually becomes urine. In glomerular hematuria, red blood cells are able to pass through the glomerular filtration barrier, leading to blood in the urine.

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52
Q
A

FIG. 1.3 KUB demonstrating residual stone fragments (arrows) adjacent to a right ureteral stent 1 week after right extracorporeal shock wave lithotripsy.

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53
Q
A

FIG. 1.4 (A) Right retrograde pyelogram performed using an 8-Fr cone-tipped ureteral catheter and dilute contrast material. The ureter and intrarenal collecting system are normal. (B) Left retrograde pyelogram using an 8-Fr cone-tipped ureteral catheter. A filling defect in the left distal ureter (arrow) is a low-grade transitional cell carcinoma. The ureter demonstrates dilation, elongation, and tortuosity, the hallmarks of chronic obstruction.

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54
Q
A

FIG. 1.5 Loopogram in a patient with epispadius/exstrophy and ileal conduit urinary diversion. (A) Plain film prior to contrast administration. (B) After contrast administration via a catheter placed in the ileal conduit, free reflux of both ureterointestinal anastomoses is demonstrated. (C) A postdrain radiograph demonstrates persistent dilation of the proximal loop indicating mechanical obstruction of the conduit (arrows).

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55
Q
A

FIG. 1.6 Normal retrograde urethrogram demonstrating (A) the balloon technique for retrograde urethrography, (B) Brodney clamp (arrowhead) technique; note the bulbar urethral stricture (arrow), and (C) normal structures of the male urethra.

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56
Q
A

FIG. 1.7 A voiding cystourethrogram performed for the evaluation of recurrent urinary tract infection in this female patient. (A) An oblique film during voiding demonstrates thickening of the midureteral profile (arrows). (B) After interruption of voiding, a ureteral diverticulum is clearly visible extending posteriorly and to the left of the midline (arrows).

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57
Q
A

FIG. 1.8 (A) Technetium 99m-mercaptoacetyltriglycine ( 99mTc-MAG3) perfusion images demonstrate normal, prompt, symmetric blood flow to both kidneys. (B) Perfusion time-activity curves demonstrating essentially symmetric flow to both kidneys. Note the rising curve typical of 99mTc-MAG3 flow studies. Dynamic function images demonstrate good uptake of tracer by both kidneys and prompt visualization of the collecting systems. This renogram demonstrates prompt peaking of activity in both kidneys. The downslope represents prompt drainage of activity from the kidneys. Printout of quantitative data shows the differential renal function to be 47% on the left, 53% on the right. The normal half-life for drainage is less than 20 minutes when 99mTc-MAG3 is used. The half-life is 5 minutes on the left and 7 minutes on the right, consistent with both kidneys being unobstructed.

58
Q
A

FIG. 1.9 Normal Technetium 99m-mercaptoacetyltriglycine ( 99mTc-MAG3) renogram of a patient with history of hydronephrosis being evaluated for obstruction. In the upper portion of the figure, a series of 2-second–per–frame flow images demonstrate the movement of radiotracer from the site of injection, to the heart, aorta/renal arteries, and kidneys. A corresponding time-activity curve is shown. The white curve reflects activity in the aorta, and the purple and teal curves reflect radiotracer activity in the kidneys. Note the sharp upstroke of all three lines and that activity in the aorta precedes activity in the kidneys by several seconds. In the lower half of the figure, a series of 2-minute–per–frame images depicts radiotracer activity within the kidneys as it transitions bilaterally into the collecting systems and then drains down the ureters. In the corresponding time-activity curve, activity within the kidneys peaks at approximately 3 to 4 minutes and then washes out, reaching half-peak approximately 6 to 9 minutes later. The split function of the kidneys is within normal limits, measuring 46% on the left and 54% on the right (red rectangle). No evidence of obstruction is present, and no furosemide is administered.

59
Q
A

FIG. 1.10 99mTc-MAG3 renogram of a patient with right-sided renal obstruction. (A) In the 2-second–per–frame flow images at the top of the panel, the left kidney appears much better perfused than the right kidney. This is borne out in the time-activity curve in the upper half of the panel in which the teal curve representing the left kidney has a significantly sharper upstroke relative to the purple curve of the right kidney. The white curve of the aorta is irregular and unreliable because of the abnormal course of the aorta caused by the patient’s scoliosis. In the bottom half of the panel, the 2-minute–per–frame images demonstrate normal transit of radiotracer through the left kidney parenchyma and into the collecting system, with drainage to the bladder. This is shown by the teal curve of the left kidney on the time-activity curve. The right kidney, which appears smaller and has a central photopenic area corresponding to a dilated renal pelvis, demonstrates increasing uptake throughout the study with very slow transit into the collecting system. This is shown by the purple curve of the right kidney in the time-activity curve. A markedly abnormal split function is present, measuring 79% on the left and 21% on the right (red rectangle). (B) Given the obstructive pattern of the right kidney, 40 mg of intravenous furosemide was administered. The 1-minute–per–frame images in the upper portion of the panel demonstrate no significant clearing of radiotracer from the left renal collecting system after furosemide administration. This is also seen in the time-activity curve, where the teal curve representing the left kidney is nearly horizontal. The lack of response to furosemide is diagnostic of an obstructed collecting system.

60
Q
A

FIG. 1.11 In this simplified schematic diagram of ultrasound imaging, the ultrasound wave is produced by a pulse generator controlled by a master clock. The reflected waves received by the transducer are analyzed for amplitude and transit time within the body. The scan converter produces the familiar picture seen on the monitor. The actual image is a series of vertical lines that are continuously refreshed to produce the familiar real-time, gray-scale image.

61
Q
A

FIG. 1.12 Midsagittal plane of the kidney. Note the relative hypoechogenicity of the renal pyramids (P) compared with the cortex (C). The central band of echoes (B) is hyperechoic compared with the cortex. The midsagittal plane will have the greatest length measurement pole to pole. A perfectly sagittal plane will result in a horizontal long axis of the kidney.

62
Q
A

FIG. 1.13 (A) Transverse view of the bladder (BL) in this female patient demonstrates the uterus (U). (B) Sagittal view of the bladder shows the uterus posterior to the bladder.

63
Q
A

FIG. 1.14 Demonstration of normal bilateral intratesticular blood flow by color Doppler.

64
Q
A

FIG. 1.15 (A) In the transverse plane scanning from the dorsal surface of the midshaft of the penis, the corpora cavernosa (CC) are paired structures seen dorsally, whereas the corpus spongiosum (CS) is seen ventrally in the midline. A calcification (Ca ++) is seen between the two CC with posterior shadowing. (B) In the parasagittal plane, the CC is dorsal with the relatively hypoechoic CS seen ventrally. Within the CC, the cavernosal artery is shown with a Ca ++ in the wall of the artery and posterior shadowing.

65
Q
A

FIG. 1.16 Normal transperineal ultrasound of the female pelvis in the midsagittal plane. The anterior compartment comprises the bladder (BL) and urethra, apical compartment comprises the vagina and uterus (UT), posterior compartment is the rectum. Source: (Image courtesy Lewis Chan, MD.)

66
Q
A

FIG. 1.17 Computed tomography (CT) of the abdomen and pelvis demonstrating normal genitourinary anatomy. (A) The adrenal glands are indicated with arrows. The upper pole of the right and left kidneys is indicated with rk and lk, respectively. a, Aorta; li, liver; p, pancreas; s, spleen; v, inferior vena cava. (B) Scan through the upper pole of the kidneys. The left adrenal gland is indicated with an arrow. a, Aorta; c, colon; d, duodenum; li, liver; lk, left kidney; p, pancreas; rk, right kidney; v, inferior vena cava. (C) Scan through the hilum of the kidneys. The main renal veins are indicated with solid arrows, and the right main renal artery is indicated with an open arrow. a, Aorta; c, colon; d, duodenum; li, liver; lk, left kidney; p, pancreas; rk, right kidney; v, inferior vena cava. (D) Scan through the hilum of the kidneys slightly caudal to C. The left main renal vein is indicated with a solid straight arrow, and the left main renal artery is indicated with an open arrow. The hepatic flexure of the colon is indicated with a curved arrow. a, Aorta; c, colon; d, duodenum; li, liver; lk, left kidney; p, pancreas; rk, right kidney; v, inferior vena cava. (E) Scan through the mid to lower polar region of the kidneys. a, Aorta; ac, ascending colon; d, duodenum; dc, descending colon; lk, left kidney; p, pancreas; rk, right kidney; rp, renal pelvis; v, inferior vena cava. (F) CT scan obtained below the kidneys reveals filling of the upper ureters (arrows). The wall of the normal ureter is usually paper thin or not visible on CT. a, Aorta; ac, ascending colon; dc, descending colon; v, inferior vena cava. (G) Contrast filling of the midureters (arrows) on a scan obtained at the level of the iliac crest and below the aortic bifurcation. ac, Ascending colon; dc, descending colon; la, left common iliac artery; ra, right common iliac artery; v, inferior vena cava. (H) The distal ureters (arrows) course medial to the iliac vessels on a scan obtained below the promontory of the sacrum. b, Urinary bladder; la, left external iliac artery; lv, left external iliac vein; ra, right external iliac artery; rv, right external iliac vein. (I) Scan through the roof of the acetabulum reveals distal ureters (solid arrows) near the ureterovesical junction. The bladder (b) is filled with urine and partially opacified with contrast material. The normal seminal vesicle (open arrows) usually has a paired bow-tie structure with slightly lobulated contour. a, Right external iliac artery; r, rectum; v, right external iliac vein. (J) Scan at the level of the pubic symphysis (open arrow) reveals the prostate gland (solid arrow). a, Right external iliac artery; m, obturator internus muscle; r, rectum; v, right external iliac vein.

67
Q
A

FIG. 1.18 Computed tomography of the abdomen and pelvis in patient with an obstructing ureteral stone at the level of the ureterovesicle junction. (A) Level of the left upper pole. Mild renal enlargement, caliectasis, and perinephric stranding are apparent. (B) Level of the left renal hilum. Left pyelectasis with a dependent stone, mild peripelvic and perinephric stranding, and a retroaortic left renal vein. (C) Level of the left lower pole. Left caliectasis, proximal ureterectasis, and mild periureteral stranding are present. (D) Level of the aortic bifurcation. The dilated left ureter (arrow) has lower attenuation than do nearby vessels. (E) Level of the upper portion of the sacrum. A dilated left ureter (arrow) crosses anteromedial to the common iliac artery. (F) Level of the midsacrum. A dilated left ureter (arrow) is accompanied by periureteral stranding. (G) Level of the top of the acetabulum showing a dilated pelvic portion of the left ureter (arrow). (H) Level of the ureterovesical junction. The impacted stone with a “cuff” or “tissue rim” sign that represents the edematous wall of the ureter. Source: (Reprinted from Talner LB, O’Reilly PH, Wasserman NF. Specific causes of obstruction. In: Pollack HM, et al., eds: Clinical urography, 2nd ed. Philadelphia: Saunders, 2000.)

68
Q
A

FIG. 1.19 A 50-year-old man with a left side pheochromocytoma and select images from a 1.5T magnetic resonance imaging. (A) Heavily weighted T2 single-shot fast spin echo with an isointense signal (not bright). (B) Moderately weighted T2 fat-suppressed fast recovery fast spin echo with hyperintense signal (bright). (C) T1-weighted precontrast images. (D) T1-weighted postcontrast images with marked early enhancement.

69
Q

Q: What are the morphologic and imaging characteristics of incidental adrenal lesions (IAL)?

A

A: Size, shape, texture, unenhanced CT attenuation (HU), 15-minute CT washout (%), MRI signal characteristics, and nuclear medicine characteristics.

70
Q

Q: What are the characteristics of adrenal metastasis IAL?

A

A: Size: Variable
Shape: Variable
Texture: Heterogeneous when larger
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): RPW <40
MRI signal characteristics: High T2 signal
Nuclear medicine characteristics: Positive on PET images

71
Q

Q: What are the characteristics of adrenal cortical carcinoma IAL?

A

A: Size: >4 cm
Shape: Variable
Texture: Variable
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): RPW <40
MRI signal characteristics: Intermediate to high T2 signal
Nuclear medicine characteristics: Positive on PET images

72
Q

Q: What are the characteristics of pheochromocytoma IAL?

A

A: Size: Variable
Shape: Variable
Texture: Variable
Unenhanced CT attenuation (HU): >10, rarely <10
15-Minute CT washout (%): RPW <40
MRI signal characteristics: High T2 signal
Nuclear medicine characteristics: Positive on MIbG

73
Q

Q: What are the characteristics of cyst IAL?

A

A: Size: Variable
Shape: Smooth, round
Texture: Smooth
Unenhanced CT attenuation (HU): <10
15-Minute CT washout (%): Does not enhance
MRI signal characteristics: High T2 signal
Nuclear medicine characteristics: Negative

74
Q

Q: What are the characteristics of adenoma IAL?

A

A: Size: 1–4 cm
Shape: Smooth, round
Texture: Homogeneous
Unenhanced CT attenuation (HU): <10 in 70%
15-Minute CT washout (%): RPW >40; APW >60
MRI signal characteristics: SI dropoff on OP images
Nuclear medicine characteristics: Variable on PET images

75
Q

Q: What are the characteristics of myelolipoma IAL?

A

A: Size: 1–5 cm
Shape: Smooth, round
Texture: Variable with macroscopic fat
Unenhanced CT attenuation (HU): <0, often <-50
15-Minute CT washout (%): No data
MRI signal characteristics: High T1 signal, India ink, variable SI dropoff on OP images
Nuclear medicine characteristics: Negative on PET images

76
Q

Q: What are the characteristics of lymphoma IAL?

A

A: Size: Variable
Shape: Variable
Texture: Variable
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): RPW <40
MRI signal characteristics: Intermediate SI
Nuclear medicine characteristics: Variable positivity on PET images

77
Q

Q: What are the characteristics of hematoma IAL?

A

A: Size: Variable
Shape: Smooth
Texture: Variable
Unenhanced CT attenuation (HU): >10, sometimes >50
15-Minute CT washout (%): No data
MRI signal characteristics: Variable signal
Nuclear medicine characteristics: Negative

78
Q

Q: What are the characteristics of neuroblastoma IAL?

A

Size: Variable
Shape: Variable
Texture: Smooth, round
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): RPW <40
MRI signal characteristics: Variable if necrotic
Nuclear medicine characteristics: Positive

79
Q

Q: What are the characteristics of ganglioneuroma IAL?

A

A: Size: Variable
Shape: Variable
Texture: Variable
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): No data
MRI signal characteristics: Usually intermediate SI
Nuclear medicine characteristics: Usually negative

80
Q

Q: What are the characteristics of hemangioma IAL?

A

A: Size: Variable
Shape: Variable
Texture: Variable
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): No data
MRI signal characteristics: Usually intermediate SI
Nuclear medicine characteristics: Usually negative

81
Q

Q: What are the characteristics of granulomatous IAL?

A

A: Size: 1–5 cm
Shape: Smooth
Texture: Usually homogeneous
Unenhanced CT attenuation (HU): >10
15-Minute CT washout (%): No data
MRI signal characteristics: Usually intermediate SI
Nuclear medicine characteristics: Positive on PET images if active

82
Q

Urologic Side Effect: Decreased libido

A

Class of Drugs: Antihypertensives
Specific Examples: Hydrochlorothiazide

83
Q

Urologic Side Effect: Erectile dysfunction

A

Class of Drugs: Psychotropic drugs
Specific Examples: Propranolol, Benzodiazepines

84
Q

Urologic Side Effect: Ejaculatory dysfunction

A

Class of Drugs: alpha-Adrenergic antagonists
Specific Examples: Prazosin, Tamsulosin, alpha-Methyldopa, Psychotropic drugs, Phenothiazines,
Antidepressants

85
Q

Urologic Side Effect: Priapism

A

Class of Drugs: Antipsychotics
Specific Examples: Phenothiazines, Antidepressants, Trazodone, Antihypertensives, Hydralazine,
Prazosi

86
Q

Urologic Side Effect: Decreased spermatogenesis

A

Class of Drugs: Chemotherapeutic agents
Specific Examples: Alkylating agents, Drugs with abuse potential, Marijuana, Alcohol, Nicotine,
Drugs affecting endocrine function, Antiandrogens, Prostaglandins

87
Q

Urologic Side Effect: Incontinence or impaired voiding

A

Class of Drugs: Direct smooth muscle stimulants
Specific Examples: Histamine, Vasopressin, Others, Furosemide, Valproic acid, Smooth muscle
relaxants, Diazepam, Striated muscle relaxants, Baclofen

88
Q

Urologic Side Effect: Urinary retention or obstructive voiding symptoms

A

Class of Drugs: Anticholinergic agents or musculotropic relaxants
Specific Examples: Oxybutynin, Diazepam, Flavoxate, Calcium channel blockers, Nifedipine,
Antiparkinsonian drugs, Carbidopa, Levodopa, alpha-Adrenergic agonists, Pseudoephedrine,
Phenylephrine, Antihistamines, Loratadine, Diphenhydramine

89
Q

Urologic Side Effect: Acute renal failure

A

Class of Drugs: Antimicrobials
Specific Examples: Aminoglycosides, Penicillins, Cephalosporins, Amphotericin, Chemotherapeutic
drugs, Cisplatin, Others, Nonsteroidal anti-inflammatory drugs, Phenytoin

90
Q

Urologic Side Effect: Gynecomastia

A

Class of Drugs: Antihypertensives
Specific Examples: Verapamil, Cardiac drugs, Digoxin, Gastrointestinal drugs, Cimetidine,
Metoclopramide, Psychotropic drugs, Phenothiazines, Tricyclic antidepressants, Amitriptyline,
Imipramine

91
Q
A
92
Q

What is the definition of microhematuria?

A

Guideline 1: 3 or more RBC/HPF on a single, properly collected urine specimen (Note: This has to be RBC seen on a microscopic exam- macroscopic blood does not count- see guideline 2 below)

Guideline 2: Clinicians should not define microhematuria by positive dipstick testing alone. A positive urine dipstick of trace blood or greater should prompt formal microscopic examination of the urine.

93
Q

What should you pay particular attention to in the initial evaluation in a person with microhematuria?

A

Guideline 3:
Perform a history and physical examination to assess risk factors for GU malignancy, medical renal disease, and non-malignant GU causes of microhemturia
-Age
-Gender
-Smoking
-LUTs
-Prior pelvic radiation
-Prior cyclophosphamide/ifosfamide chemo
-Exposure to dyes/chemicals
-Indwelling foley
-Family history of UC or lynch syndrome

Guideline 5: In persons with findings suggestive of a non-malignant or gynecology etiology, these persons should be evaluated with appropriate physical examination techniques and tests to identify the etiology. (IE: do a pelvic exam in women)

94
Q

How do you evaluate a person on anticoagulants or anti platelet drugs with microhematuria?

A

Guideline 4: They should have the same evaluation as someone not on these drugs.

95
Q

If a person is identified as having an UTI or a gynecology or non-malignant GU cause of having microhematuria, are you done with evaluation?

A

Guideline 6/7: You must obtain a urinalysis with microscopic examination to ensure resolution of the hematuria. If it persists or you can’t identify the etiology, you should perform a risk-based assessment of the microhematuria.

*** The panel acknowledges that there are some non-malignant causes such as BPH, nephrolithiasis, vaginal atrophy or prolapse, in which the MH won’t completely resolve even with appropriate management. In these cases you must use judgement and careful shared decision making to decide to pursue MH evaluation.

96
Q

If a person is thought to have microhematuria secondary to medical renal disease are you done with evaluation?

A

Guideline 8: Refer these patients to nephrology. but still do a risk based urological evaluation.

97
Q

What are the low, intermediate and high risk categories of microhematuria?

A

Low risk (must meet all criteria): women age < 50, men age < 40, never smoker or < 10 pack years, 3-10 RBC/HPF on a single UA, no risk factors for GU malignancy

Intermediate risk (meet any one criteria): women age 50-59, men age 40-59, 10-30 pack years, 11-25 RBC/HPF on a single UA, repeat UA in a low risk patient with repeat 3-10 RBC/HPF, additional risk factors for UC.

High risk (meet any one criteria): Women or men >59 years, > 30 pack years, > 25 RBC/HPF, any gross hematuria

98
Q

How should you treat a low risk person with microhematuria?

A

Guideline 10: Clinicians should engage in shared decision making to decide between repeating UA within 6 months or proceeding with cystoscopy and renal bladder ultrasound.

99
Q

How should you treat a low risk patient who has a repeat microhematuria who elected not to undergo initial evaluation?

A

Guideline 11: You should reclassify these patients as intermediate or high risk and perform cystoscopy with upper tract imaging

100
Q

How should you work up an intermediate risk patient with microhematuria?

A

Guideline 12: Clinicians should perform cystoscopy and renal ultrasound

101
Q

How should you work up a high risk hematuria patient?

A

Guideline 13: Cystoscopy and upper tract imaging:
1st preference is multiphasic CT urography (if GFR >30 and no iodine allergy)
2nd preference is MR urography
3rd preference is retrograde pyelography with non-contrast axial imaging or renal ultrasound

Special exception: pregnant women get RUS with axial imaging after delivery

102
Q

What type of cystoscopy should you perform in a person with microhematuria?

A

Guideline 14: Clinicians should perform white light cystoscopy as part of the workup (blue light costs more money, time and has not been studied in this setting and may lead to unnecessary biopsies- it is NOT currently recommended)

103
Q

What may you do in someone with persistent microhematuria previously worked up by renal ultrasound?

A

Guideline 15: Perform additional imaging of the upper urinary tract

104
Q

What should you do in a intermediate risk patient with a family history of RCC or a known genetic renal tumor syndrome?

A

Guideline 16: You should get upper tract imaging

(known genetic renal tumor syndromes are: VHL, BHD, hereditary papillary RCC, hereditary leiomyomatosis RCC, and tuberous sclerosis)

105
Q

What is the role of urinary markers in the workup of microhematuria?

A

Guidelien 17: Do not use urine cytology or makers in the initial evaluation of microhematuria

Guideline 18: You may obtain urine cytology for patients with persistent microhematuria after a negative work up who have irritative voiding symptoms or risk factors for CIS

106
Q

After a negative microhematuria workup, how often should you repeat a urinalysis?

A

Guideline 19: Within 12 months

107
Q

After a negative microhematuria evaluation and negative subsequent urinalysis, what should you do?

A

Guideline 20: the UA should be repeated in 12 months after an initial negative evaluation. However, if the subsequent UA is negative, you can stop any further workup

108
Q

For persons with a prior negative microhematuria workup and persistent microhematuria, what is recommended?

A

Guideline 21: Shared decision making regarding need for additional workup

109
Q

For persons with a prior negative microhematuria workup and worsening microhematuria or gross hematuria or new symptoms, what is recommended?

A

Guideline 22: It is recommended that you have further workup though what this workup entails is not specified and it ultimately says this should be shared decision making based on patient preferences and physician judgement…..

110
Q

Characterization of gross hematuria depending on the phase and explain indication

A
  1. Initial–> urethral source 2. Terminal –> Trigone,neck prostate 3. Total hematuria –> Bladder and above
111
Q

causes of pigmenturia mimicking GH:

A
  1. Endogenous sources (Bilirubin, myoglobin, porphyrins) 2. Food (Beets, rhubarb) 3. Drugs (phenazopyridine) 4. simple dehydration
112
Q

AUA definition of microscopic hematuria

A

3 or more / HPF

113
Q

causes of false positives for MH, cause of false negative

A

first void urine and post sexual activity might cause false positive Dilute urine (<308 osm) -> might cause false negative

114
Q

The likelihood of identifying a malignancy has been found to be greater among patients with higher levels of MH _ RBC/HPF, GH, or risk factors for malignancy

A

>25 rbc/hpf

115
Q

Common Risk Factors for Urinary Tract Malignancy in Patients With Microscopic Hematuria

A
116
Q

Patients who develop hematuria who are taking anticoagulaton or antiplatelet medications should undergo _____.

A

patients who develop hematuria (microscopic or gross) who are taking anticoagulation or antiplatelet medications (e.g., warfarin, enoxaparin, heparin, aspirin, clopidogrel, nonsteroidal anti-inflammatory agents) should undergo a complete evaluation in the same manner as patients not taking such medications

117
Q

In women, the ACOGAU society recommend/does not recommend evaluation for asymptomatic MH for patients that has never smoked aged 33-50 who have <25 hpc. What is the rate of Urinary tract for this malignancy for this patients

A

does not recomment, <0.5%

118
Q

Blue light cystoscopy uses _____ or ____ instillation

AUA recommends for/against using blue-light cystoscopy for evaluation of MH

A

5-aminolevulinic acid ALA or Hexyl aminolevulinate (HAL)

Against

119
Q

the imaging of choice by the AUA for evaluation of asymptomatic MH

A

Multiphasic ct urogram

120
Q

36/F patient consulted for Asymptomatic MH,noted no infection, no menstruation,no urologic procedures, what is the next step for workup

A

Renal function testing, cystoscopy imaging CTU. COncurrent workup for proteinuria and red cell morphology to see if there is nephrological cause.

If negative for the following, the patient may follow-up at least one UA/Micro yearly for at least 2 years. If still with persistent MH, annual must be done. Repeat anatomic evaluation within 3-5 years if clinically indicated

121
Q

patients presenting with GH in the absence of antecedent ___ or____ should be evaluated with a ____ examination, ___ and ____

A

patients presenting with GH in the absence of antecedent trauma or culture-documented UTI should be evaluated with a urine cytologic examination, cystoscopy, and upper tract imaging, preferably CT urogram.

122
Q

_____________, a member of the ____ family, is the most common virus associated with hemorrhagic cystitis

A

BK virus, polyomavirus

123
Q

treatment for viral hemorrhagic cystitis is:___

A

primarily supportive, with hydration, diuresis, and bladder irrigation, although case reports of success with antiviral therapy exist

124
Q

Chemotherapeutic drugs that cause Hemorrhagic cystitis

Bladder toxicity results from renal excretion of the metabolite ___, which is produced by the liver and stimulates bladder mucosal sloughing and subsequent tissue edema/fibrosis

____, which binds to ___ and renders it inert, has been suggested for prophylaxis against cyclophosphamide-induced hemorrhagic cystitis

A

cyclophosphomide and iphosphamide

Bladder toxicity results from renal excretion of the metabolite acrolein, which is produced by the liver and stimulates bladder mucosal sloughing and subsequent tissue edema/fibrosis

2-Mercaptoethane sulfonate (mesna), which binds to acrolein and renders it inert, has been suggested for prophylaxis against cyclophosphamide-induced hemorrhagic cystitis

125
Q

what is the initial management for HC? next step if initial management for hemorrhagic cystitis is not effective:

A

Hyperbaric oxygen therapy

126
Q

this agent may be considered for first-line intravesical therapy among patients with hemorrhagic cystitis failing initial supportive measures, particularly among those without renal insufficiency.

A

Alum, aluminum ammonium sulfate or aluminum potassium sulfate) may be dissolved in sterile water (50 g alum in a 5-L bag of sterile water [1% alum solution]) and then used to irrigate the bladder at a rate of 200 to 300 mL/h.

127
Q

A lysine analogue, aminocaproic acid is a competitive inhibitor of activators of plasminogen, including urokinase, and thus interrupts fibrinolysis and the cascade that perpetuates hemorrhage

A

aminocaproic acid

Continuous bladder irrigation with 200 mg aminocaproic acid/L of 0.9% normal saline has been described, with irrigation continued for 24 hours after hematuria resolves.

128
Q

mechanism of HBOT

A

local tissue oxygen tension increases and thus oxygen extraction by tissues increases, thereby diminishing edema and promoting neovascularization, all of which are critical steps in the wound healing process

129
Q

BPH/Prostate Cancer represents the most common cause of prostate-related bleeding and has been cited as the most common cause of GH in men older than ___

A

BPH represents the most common cause of prostate-related bleeding and has been cited as the most common cause of GH in men older than 60

130
Q

The cause for BPH-related hematuria has been thought to be increased prostatic vascularity resulting from ____ in hyperplastic prostate tissue This noted increase in microvessel density has in turn been linked to higher levels of _____

A

The cause for BPH-related hematuria has been thought to be increased prostatic vascularity resulting from higher microvessel density in hyperplastic prostate tissue This noted increase in microvessel density has in turn been linked to higher levels of vascular endothelial growth factor (VEGF)

131
Q

Treatment with finasteride is associated with decreased ___, prostate ___ and __

A

Treatment with finasteride is associated with decreased VEGF expression (Pareek et al., 2003), prostate microvessel density (Pareek et al., 2003), and prostatic blood flow

132
Q

“Nutcracker syndrome” (i.e., renal vein entrapment syndrome) is defined as the compression of the left/right renal vein between the __ and the superior ___

tx for nutcracker syndrome

A

“Nutcracker syndrome” (i.e., renal vein entrapment syndrome) is defined as the compression of the left renal vein between the abdominal aorta posteriorly and the superior mesenteric artery anteriorly.

Left renal vein transposition, superior mesenteric artery transposition, and nephrectomy have been described as surgical approaches for management of this condition

133
Q

According to AUA guidelines, microhematuria sufficient to trigger a diagnostic evaluation is defined as:

a. a positive chemical test (urine dipstick) showing small, moderate, or large blood on one properly collected specimen.
b. a positive chemical test (urine dipstick) showing small, moderate, or large blood on at least two of three properly collected specimens.
c. a positive chemical test (urine dipstick) showing large blood on one properly collected specimen.
d. urine microscopy showing three or more red blood cells per high-powered field on one properly collected urine specimen.
e. urine microscopy showing three or more RBC/HPF on at least two of three properly collected urine specimens

A

. d. Urine microscopy showing three or more red blood cells per high-powered field on one properly collected urine specimen. The presence of three of more RBCs/HPF on a single urine microscopy is associated with malignancy in 2.3-5.5% of patients. Chemical tests for hematuria detect the peroxidase activity of erythrocytes using benzidine, and can render false results in the presence of dehydration, myoglobinuria, high doses of vitamin C, improper technique, and other factors. While higher levels of microhematuria (>25 RBCs/HPF) are known to be associated with higher rates of malignancy on evaluation, setting the threshold higher than three RBCs/HPF or requiring more than one positive urinalysis would lead to an unknown number of missed opportunities for diagnosis

134
Q

The likelihood of finding a malignancy in a patient with microhematuria is influenced by all of the following EXCEPT: a. age. b. gender. c. use of anticoagulants. d. tobacco use. e. degree of hematuria.

A

c. Use of anticoagulants. Increasing age, male gender, and tobacco use are risk factors for urologic cancers and specifically for urothelial carcinoma. In addition, while there is little data to distinguish among thresholds of two, three, four, or five RBCs/HPF, it is clear that a high level of microhematuria (>25 RBCs/HPF) is associated with a greater likelihood of malignancy. By contrast, patients using anticoagulant medications or antiplatelet medications have a similar risk of malignancy compared to those who do not use these medications. Therefore such patients should be evaluated comparably to those who do not use anticoagulants or anti-platelet agents

135
Q

According to AUA guidelines, the proper initial assessment of a 50- year-old patient with asymptomatic microhematuria includes:

a. blood pressure measurement, serum creatinine level, cystoscopy, and computed tomography (CT) urogram.
b. urine cytology, cystoscopy, and CT urogram. c. urine cytology, blue-light cystoscopy, and any upper tract imaging. d. urine cytology and renal/bladder ultrasound. e. no evaluation is necessary unless microhematuria is persistent/recurrent or hematuria is visible

A

a. Blood pressure measurement, serum creatinine level, cystoscopy, and computed tomography (CT) urogram. The AUA suggests that adult patients presenting with asymptomatic microhematuria should undergo evaluation to determine the cause. Blood pressure measurement and serum creatinine level may help identify patients who require concurrent nephrologic workup, and creatinine level also helps determine patient eligibility for contrast imaging. The evaluation of asymptomatic hematuria includes imaging (preferably with CT urogram), and cystoscopy in patients 35 and older and those under 35 with risk factors for malignancy

136
Q

In the evaluation of patients with microhematuria, cystoscopy may be safely avoided if: a. there are no associated symptoms in a patient of any age. b. the patient is under 35 years of age and without symptoms or risk factors for malignancy. c. the patient is taking aspirin or warfarin. d. the cytology is negative. e. the patient has a history of urinary tract infection and hematuria is still present after treatment

A

b. The patient is under 35 years of age and without symptoms or risk factors for malignancy. The AUA guidelines ( Fig. 16.1 ) call for use of cystoscopy for evaluation of hematuria in all patients 35 years of age and older (Recommendation). The risk of malignancy is very low in persons under 35 years of age, such that the potential benefits of cystoscopy may be outweighed by the very small risks associated with the procedure. Therefore it is an option to omit cystoscopy in patients under the age of 35, provided that the patient does not have risk factors for a urologic malignancy.

137
Q

Patients presenting with gross hematuria in the absence of recent trauma or concurrent infection who are on anticoagulation medications should be evaluated with: a. urinalysis, urine cytology, and cystoscopy only. b. CT urogram, with cystoscopy only if symptomatic. c. no evaluation necessary. d. assessment of anticoagulation status, and evaluation only if supra-therapeutic. e. urine cytology, cystoscopy, CT urogram.

A

e. Urine cytology, cystoscopy, CT urogram. Given the increased frequency with which clinically significant findings are associated with gross hematuria, the recommended evaluation in this setting is relatively uniform. That is, patients presenting with gross hematuria in the absence of antecedent trauma or culture-documented urinary tract infection should be evaluated with a urine cytology, cystoscopy, and upper tract imaging, preferably CT urogram. Importantly, patients who develop hematuria who are on anticoagulation medications should undergo a complete evaluation in the same manner as patients not taking such medications, as the prevalence of hematuria, as well as the likelihood of finding genitourinary cancers, among patients with hematuria on anticoagulation has been reported to be no different from patients not taking such medications.

138
Q

The metabolite of oxazaphosphorine chemotherapeutic agents which is responsible for hemorrhagic cystitis is: a. Mesna. b. Acrolein. c. Formalin. d. Gemcitabine. e. Methotrexate.

A

b

139
Q

Use of intravesical alum for hemorrhagic cystitis should be avoided in patients with: a. a history of malignancy. b. a history of detrusor instability. c. active gross hematuria. d. renal insufficiency. e. vesicoureteral reflux

A

d. Renal insufficiency. Alum may be considered for first-line intravesical therapy among patients with hemorrhagic cystitis ( Fig. 16.2 ) failing initial supportive measures. However, while cell penetration and therefore overall toxicity of this agent are low, systemic absorption may nevertheless occur and may result in aluminum toxicity, with consequent mental status changes, particularly among patients with renal insufficiency. Meanwhile, prior to intravesical administration of silver nitrate or of formalin, a cystogram should be obtained to evaluate for the presence of vesicoureteral reflux.

140
Q

A 35-year-old man presents with complaint of penile pain and immediate detumescence during intercourse. Physical examination notes blood at the urethral meatus. The next step should be: a. immediate operative exploration. b. CT scan of pelvis. c. retrograde urethrography. d. obtain serum coagulation parameters. e. conservative management with serial examinations.

A

Retrograde urethrography. The clinical scenario is consistent with an acute penile fracture. Blood at the meatus raises suspicion for concomitant urethral injury that requires investigation by retrograde urethrography prior to planned operative repair. Conservative management poses the risk of untreated urethral and corporal injury that can result in urethral stricture disease and erectile dysfunction. 11. b. Renal angiography.

141
Q

Alum may be used as a first-line intravesical therapy for hemorrhagic cystitis in patients ___ . Formalin is a highly effective form of intravesical therapy for hemorrhagic cystitis. A ____ should be obtained before therapy to ensure no ____

A
  1. Alum may be used as a first-line intravesical therapy for hemorrhagic cystitis in patients without renal dysfunction. 11. Formalin is a highly effective form of intravesical therapy for hemorrhagic cystitis. A cystogram should be obtained before therapy to ensure no vesicoureteral reflux.
142
Q
A