Chapter 12 Flashcards

1
Q

lab values for post renal azotemia

A

During early stage of obstruction, increased tubular pressure “forces” BUN into the blood (serum BUN:Cr ratio > 15); tubular function remains intact (FENa < 1% and urine osm > 500 mOsm/kg).

With long-standing obstruction, tubular damage ensues, resulting in decreased
reabsorption of BUN (serum BUN:Cr ratio < 15),

**THIS IS BECAUSE REABS OF BUN REQUIRES AN INTACT TUBULE

decreased reabsorption of sodium (FENa > 2%), and inability to concentrate urine (urine osm < 500 mOsm/kg).

***ALSO REQUIRES AN INTACT TUBULE

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2
Q

Injury and necrosis of tubular epithelial cells (Fig. 12.5); most common cause of acute renal failure aka…

A

intrarenal azotemia

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3
Q

most common causes of ATN

A

Causes include aminoglycosides (most common), heavy metals (e.g., lead),
myoglobinuria (e.g., from crush injury to muscle), ethylene glycol (associated with oxalate crystals in urine), radiocontrast dye, and urate (e.g., tumor lysis syndrome).

these are nephrotoxic

ischemia can also cause this

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4
Q

what is acute interstitial nephritis? what may it progress to?

A

A. Drug-induced hypersensitivity involving the interstitium and tubules results in acute renal failure (intrarenal azotemia)

B. Causes include NSAIDs, penicillin, and diuretics.

C. Presents as oliguria, fever, and rash days to weeks after starting a drug; eosinophils may be seen in urine.

D. Resolves with cessation of drug

E. May progress to renal papillary necrosis

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5
Q

as more water gets reabsorbed in prerenal azotemia….as does…

A

the BUN

that’s how you get a BUN to creatinine ratio greater than 15

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6
Q

PRERENAL AZOTEMIA OFTEN DEVELOPS INTO

A

ATN aka INTRARENAL AZOTEMIA

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7
Q

*WHY are these the lab values for INTRARENAL AZOTEMIA

decreased reabsorption of BUN (serum BUN:Cr ratio < 15), decreased reabsorption of sodium (FENa > 2%), and inability to concentrate urine (urine osm < 500 mOsm/kg)

????

A

Dysfunctional tubular epithelium!!!!! can’t reabs BUN and can’t really reabs sodium!!!

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8
Q

what are angiomyolipomas in the kidney? what are they associated with?

A

ANGIOMYOLIPOMA
A. Hamartoma comprised of blood vessels, smooth muscle, and adipose tissue
B. Increased frequency in tuberous sclerosis

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9
Q

what are renal cell carcinomas associated with?

A

Paraneoplastic syndromes!!!! (e.g., EPO, renin, PTHrP, or ACTH) may also be present.

Rarely may present with left-sided varicocele

Involvement of the left renal vein by carcinoma blocks drainage of the left spermatic vein leading to varicocele.

Right spermatic vein drains directly into the IVC; hence, right-sided varicocele is not seen.

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10
Q

what gene is renal cell carcinoma pathogenesis?

A

Pathogenesis involves loss of VHL (3p) tumor suppressor gene, which leads
to increased IGF-1 aka insulin like GF (promotes growth) and increased HIF transcription factor (increases VEGF and PDGF).

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11
Q

what are the two pathways to get RCC?

A

Tumors may be hereditary or sporadic.
1. Sporadic tumors classically arise in adult males (average age is 60 years) as a
single tumor in the upper pole of the kidney; major risk factor for sporadic
tumors is cigarette smoke.
2. Hereditary tumors arise in younger adults and are often bilateral.
i. Von Hippel-Lindau disease is an autosomal dominant disorder associated with inactivation of the VHL gene leading to increased risk for hemangioblastoma of the cerebellum and renal cell carcinoma.

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12
Q

what is VHL disease?

A

Von Hippel-Lindau disease is an autosomal dominant disorder associated with inactivation of the VHL gene leading to increased risk for hemangioblastoma of the cerebellum and renal cell carcinoma.

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13
Q

what is wilms tumor and how does it present?

A

Malignant kidney tumor comprised of blastema (immature kidney mesenchyme), primitive glomeruli and tubules, and stromal cells (Fig. 12.20)
1. Most common malignant renal tumor in children; average age is 3 years.
B. Presents as a large, unilateral flank mass with hematuria and hypertension (due to renin secretion)

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14
Q

what are the two strange syndromes that Wilms tumor is associated with?

A

Associated with WTI mutation, especially in syndromic cases

  1. WAGR syndrome-Wilms tumor, Aniridia, Genital abnormalities, and mental and motor Retardation
  2. Beckwith-Wiedemann syndrome-Wilms tumor, neonatal hypoglycemia, muscular hemihypertrophy, and organomegaly (including tongue)
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15
Q

what are the only three bladder cancers that i need to worry about?

A
  • urothelial cancer
  • squamous cell carcinoma
  • adenocarcinoma
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16
Q

risk factors of urothelial cell carcinoma

A

Malignant tumor arising from the urothelial lining of the renal pelvis, ureter, bladder, or urethra
1. Most common type of lower urinary tract cancer; usually arises in the bladder

B. Major risk factor is cigarette smoke; additional risk factors are naphthylamine, azo dyes, and long-term cyclophosphamide or phenacetin use.

17
Q

which urothelial cell carcinoma is worse- flat or papillary?

A

Arises via two distinct pathways (Fig. 12.21)

  1. Flat-develops as a high-grade flat tumor and then invades; associated with early p53 mutations
  2. Papillary-develops as a low-grade papillary tumor that progresses to a high- grade papillary tumor and then invades; not associated with early p53 mutations
18
Q

risk factors of squamous cell carcinoma

A

Risk factors include chronic cystitis (older woman), Schistosoma hematobium
infection (Egyptian male), and long-standing nephrolithiasis.

19
Q

risk factors of adenocarcinoma of the bladder

A

Malignant proliferation of glands, usually involving bladder
B. Arises from a urachal remnant (tumor develops at the dome of the bladder), cystitis glandularis, or exstrophy (congenital failure to form the caudal portion of the anterior abdominal and bladder walls)

20
Q

mmmmkay go look over nephritic and nephrotic!! that’s all you can do chica!! remember you are the luckiest girl in the whole world

A

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