Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
192 Cards in this Set
- Front
- Back
Why does the ureter not have a serosa?
|
Because it is retroperitoneal. Only Intraperitoneal structures have it.
|
|
Of a tumor invaded the lamina propria but not the muscularis, is it considered low or high stage?
|
Low
|
|
Name the cell layers of of the UTI tract from out to in.
|
Transitional epithelium, basement membrane, lamina propria, muscularis, adventitia
|
|
Tumor that has not invaded the basement membrane is called?
|
Carcinoma Insitu
|
|
What is another name for transitional epithelium?
|
Urothelium
|
|
T/F: Von Brunn Nests can give rise to neoplasia
|
True
|
|
T/F Von Brunn nests can only occur in the ureter.
|
False, also can occurs in bladder
|
|
What is the pathogenesis of double ureter
|
Double or split uretic bud
|
|
Congenital megaloureter is associated with what condtion?
|
Hirsprung (Megacolon) dz
|
|
What is the complication of congential megaloureter?
|
The ureter doesn't, this leads to dilation, which could cause hydronephrosis and renal failure.
|
|
What is the cause of ureteritis cystica? Can it become metaplastic?
|
Chronic inflammation? yes
|
|
A calculi can get stuck in what three places?
|
UPJ, Iliac vessals, bladder entrance----becaues the ureter is narrower at this sites.
|
|
Ergot Derivatives and b-blockers are the known drug causes for what ureteral disorder?
|
Sclerosing retroperitoneal fibrosis.
|
|
Sclerosing retroperitoneal fibrosis is caused by what other conditions?
|
Sclerosing cholangitis
Sclerosing mediastinitis Ridell's fibrosing thyroiditis Lymphoma AND idiopathic |
|
What is the complication of sclerosing mediastinitis?
|
Hydronephrosis due to obstruction of the ureter.
|
|
What is the most common neoplasm in the ureter?
|
TCC
|
|
What are the risk facts for TCC of the ureter.
|
Same as that of the bladder (smoking, etc)
|
|
what is the clinical significance of a transition cell carcinoma?
|
It causes obstruction
|
|
This condition can black venous drainage of the right spermatic vein cause right scrotal varicocele?
|
Sclerotic retroperitoneal fibrosis
|
|
Pt with this condition has feces draining out of the umbillicus.
|
Perisitent (Vitelline) Sinus
|
|
Pt with this condition has urine draining out of his umbillical
|
Persistant urachus sinus. (urachal cysts)
|
|
Having urachal cysts predisposes one to?
|
Adenocarcinoma of the bladder.
|
|
What is the most common acquired cause of bladder diverticula?
|
BPH
|
|
What are the complications of bladder diverticula?
|
Diverticulitis and calculi
|
|
Exostrophy of the bladder is related to what condition?
Predisposed to? and how? |
Epispadias
Adenocarcinoma because of glandular metaplasia due to inflammation. |
|
What is the most common cause of bladder adenocarcinoma?
|
Urachus remnant
|
|
What is the most common urinary pathogen?
Most common bacterial infection in elderly. Most common cause of sepsis in hospitalized pts? |
E. Coli
E. Coli E. Coli |
|
MC viral cause of hemorrhagic cystitis?
|
Adenovirus
|
|
Name 4 causes of acute cystitis.
|
E. Coli MC
Staphylococcus saprophyticus Adenovirus Acute urethral syndrome |
|
2nd cause of Acute cystitis in sexually active women, what bug?
|
Staph saprophyticus
|
|
What is the MCC of acute urethral syndrome?
|
Clamydia Trachomonus
also mycoplasma, ureaplasma, neisseria gonorrhea |
|
Acute urethral syndrome in women is analogous to what in men?
|
non-specific urethritis
|
|
T/F: acute and chronic cystitis usually present with fever?
|
False. fever usually means acute pyelonephritis
|
|
What are the signs of acute and chronic cystitis?
|
Dysuria, frenquency, urgency, nocturia, suprapubic pain, gross hematuria
|
|
Another name for interstitial cystitis? is it acute or chronic?
|
Hunner's ulcer
Chronic |
|
What is the histology of Hunner's ulcer.
|
Inflammation and fibrosis involving all layers of bladder with MAST CELLS.
|
|
What is the probable cause of Hunner's ulcer?
|
Autoimmune
|
|
Who of asymtomatic bacteriuria in women
|
Pregnant women, elderly women in nursing home, diabetic women
|
|
Pt comes in your with Hunner's ulcer, what do you do first?
|
Biopsy it, to rule out carcinoma
|
|
What are causes of sterile pyuria?
|
Clamydia, Renal tuberculosis, acute tubulointerstitial nephritis.
|
|
Malakoplakia is related to?
Who usually get it? |
Chronic E. Coli infectino of the bladder.
Immunosuppressed folks. |
|
What is the histology of malakoplakia?
|
Foamy macrophages filled with mineralized secretions. Michalis Guttman bodies
|
|
Do cystitis cystic and glandularis have Von Brunn Nests
|
YES they do
|
|
Transitional cell papilloma: is it benign or malignant? Common or rare. How does it look?
|
Rare benign tumor. Some consider it a low grade transitional cell carcinoma. It looks like a wart.
|
|
What are the causes of transitional cell carcinoma?
|
Smoking
Aniline dyes Cyclophosphamide Schistosoma Hematobium LONG TERM ANALGESIC USE |
|
What chromosomal event is related to transitional cell carcinoma?
|
Deletion of chromosome 9
|
|
TCC is more common in?
|
Male
|
|
Three causes of adenocarcinoma of the bladder?
|
Urachal remnant (MCC)
Cytitis glandularis Exostrophy of the bladder |
|
what is the most common sarcoma in children? Where is it most common in boys? girls?.
|
Embryonal rhabdomyosarcoma (sarcoma botryoides).
Urinary system-urethra=boys. Vagina=girls |
|
A boy with a grape like mass protruding from urethral orifice, what is it?
|
Embryonal rhabdomyosarcoma
|
|
In the TNM staging system, what do TIS, T1, T2 mean.
|
TIS = Carcinoma In Situ
T1 = in lamina propria T2 = in muscularis |
|
Most common sites of bladder transitional cell carcinoma?
|
Lateral or posterior wall at the base of the bladder.
|
|
Do TCC tumors that have the A, B, H antigens have better or worse prognosis?
|
Better
|
|
What are the complications of bladder that invade the bladder?
|
Hydronephrosis, post-renal azotemia, death by renal failure
|
|
Squamous cell carcinoma of bladder is caused by. How is the histology?
|
Schistosoma Haematobium - chronic inflammation
Egg with nipple on end. Egg is surrounded by Eosinophils that try to kill it w/ type II hypersensitivity --> chronic inflammation --> squamous metaplasia |
|
Invasive cervical or prostate carcinoma common invade what? and so what is the cause of death?
|
Bladder.
Obstruction-> hydronephrosis-->renal failure |
|
Three symptoms of Reiters syndrome in men.
A common component of which is? |
Urethritis
Conjunctivitis (sterile) HLA-B27 arthritis Chlamydia urethritis |
|
What is the mos common carcinoma of urethra?
Who gets it? Usually involve? |
Squamous cell carcinoma.
Older patients External meatus |
|
Urethral Caruncle dominant in male or female?
|
female.
|
|
Causes of urinary tract obstructions:
|
Congenital anomalies (posterior urethral valves, strictures)
Stones, Tumors, inflammations, sloughed papilla, blood clots, pregnancy, uterine prolapse, functional disorders |
|
E. Coli causes cystitis in women and what in men?
|
Protatitis
|
|
Stones are more common in males or females?
|
Males
|
|
Most common type of stones. what are the common risk factors?
|
Calcium phoshate or calcium oxylate.
Hypercalciumia, hyperphosphatemia, and high pH |
|
What are "triple stones" made of? what are the other names?
Are they formed at high or low pH |
Magnesium ammonium phosphate.
Struvite, staghorn. 2nd most common stone. high pH (NOT LOW) |
|
Uric acid stones and cystic stone, which is more common
|
Uric acid (6%)
Cystine is only 1-2 % |
|
Is BPH a risk factor for carcinoma?
|
NO
|
|
How does BPH affect the bladder?
|
Obstruct --> hypertrophy
|
|
In cystocele, the bladder is pulled into the vagina by?
|
The prolapsing uterus due to the weekend pelvic floor.
This creates a pouch that collects residual urine --> problems |
|
What congenital abnormality of the kind is related to Turner Syndrome
|
Renal agenesis
|
|
Unilateral renal agenesis is more common in male or females? Which side is more frequent? It is a predisposition for what?
|
Males.
Left side Vesicoureteral reflux |
|
Horseshoe kidney more in male or females?
|
Male
|
|
What is the most common cause of Acute Renal Failure.
What are the other causes? |
Acute tubular necrosis.
Post renal obstruction (ex BPH), Vascular dz (malignant HTN,RPGN, DIC, Urate Nephropathy. |
|
Name to main causes of ATN
|
Ischemic and Nephrotoxic
|
|
What is the pathogenesis of ischemic ATN.
|
1. Hypoxia damages endothelial cells --> decrease vasodilators (NO2, PGI2), increase vasoconstrictors (endothelin)--> Vasoconstriction of afferent arterioles --> decrease GFR.
1. Ischemia also kills tubules cells, it sloughs and obstruct (make pigmented tubular cell casts)-> cast obstruct lumen, dec GFR, push fluid into interstitium --> oliguria |
|
What is the most common site of tubular damnage in ischemic ATN?
|
The straight segment of prox tubule and medullary segment of thick ascending limb. The BM is affected so tubular cells can't regenerate.
|
|
Name the causes of nephrotoxic ATN. (MCC?)
|
Aminoglycosides (most common)
Radiocontrasts Heavy metals (lead, mercury) |
|
Which ATN is reversible, why?
|
Nephrotoxic ATN, because the basement membrane is still intact.
|
|
Where is the damage in nephrotoxic ATN?
|
Proximal tubular cells
|
|
Clinical findings of ATN
|
Oliguria, in most cases
Pigmented renal tubular cell casts Hyperkalemia, increased anion gap metabolic acidosis Hypokalemia (diuresis phase) and infection are common problems |
|
What are three stages of ATN?
|
Initial stage (first 36 hrs), Oliuria, Diuretic
|
|
Causes on tubulointerstitial nephritis (TIN). Most common cause?
|
Acute pyelonephritis
Drugs Infection SLE, lead poisoning, urate nephropathy, multiple myeloma |
|
Most common cause of acute pyelonephritis. It is more common in
|
Ascending infections.
Female (short urethra) |
|
What are the risk factors for acute pyelonephritis
|
Urinary tract obstruction (reflux),
Medullar sponge dz, DM, Sickle cell dz/trait |
|
Pathogenesis of acute pyelonephritis caused by reflux (ascending inf)
|
The intravesicular region is not compressed during micturition --> Reflux of urine into bladder
|
|
What is the gross and microscopic histlogy of acute pyelonephritis?
|
Gray and white areas of abscess formation in cortex and medulla, micro abscess in tubular lumens and interstitium
|
|
Lab findings of acute pyelonephritis?
|
WBC casts (key finding)
Pyuria, bacteriuria (usually E. coli), hematuria |
|
Acute pyelonephritis can lead to these complications:
|
Chronic pyelonephritis
Perinephric abscess Renal papillar necrosis |
|
Two causes of chronic pyelonephritis (CPN)
|
VUR starting in young girls
Urinary tract obstruction (BPH etc) |
|
Gross finding of obstructive CPN? Reflux type?
|
Dilation of calyces
Diffuse thinning of cortical tissue Cortical Scar Over blunt calyx |
|
What is thyroidization?
|
Tubular atrophy in CPN
|
|
Drug Induced tubulointerstitial nephritis (TIN) is associated with what drugs?
|
Pennicillins, Rifampin, Sulfonamides, NSAIDS, Diuretic
|
|
Pathogenesis for drug induced TIN. Is it reversible?
How is the BUN/Cr ratio? |
Combination of type I and type IV hypersensitivity
Occurs ∼2 weeks after beginning a drug. Yes it is reversible BUN/Cr < 15 (renal) |
|
What is the most predictive lab finding in drug induced TIN?
|
Eosinophilia, and eosinophiluria ===> it's an allergic reaction.
|
|
What is the most common cause of drug induced TIN?
|
Analgesic nephropathy
|
|
Is analgesic nephropathy more common in males or females?
It occurs in what other patients? |
Females.
People with chronic pain who takes lots of analgesic |
|
Pathogenesis of analgesic nephropathy.
|
Chronic pain-> use of acetaminophen + aspirin for more than 3 yrs.
Acetaminophen - free radical damnage to tubular cells in medulla. Aspirin decreases PGI2 --> decrease O2 supply to medulla. |
|
Complications of analgesic nephropathy.
|
Renal papillar necrosis (colicky pain, ring defect where papilla used to be)
HTN-> Chronic renal failure Transitional Cell carcinoma of the renal pelvis and bladder |
|
How does urate nephropathy affect kidney?
Who gets it? |
Deposition of urate crystals in tubule and interstitium
Leukemia pt (acute), gout (chronic), lead poisoning |
|
How does lead poisoning lead to urate nephropathy? (indirect effect)
What does the direct effect of lead cause? |
Lead decrease secretion of uric acid in kidney. In direct effect.
Tubulointersitial nephritis |
|
How multiple myeloma cause renal dz.
|
1. Bence Jones protein produce tubular casts, light chains are toxic to tubular epithelium. Cast obstruct lumen and start a foreign body giant cell reaction.--> renal failure
2. Nephrocalcinosis (hypercalcemia) - Metastatic calcification of the basement membrane of collecting tubules 3. Light chains make amyloid --> amylodosis (nephrotic syndrome) |
|
Most common cause of Chronic Renal failure (decending)
|
Diabete mellitus
HTN Glomerulonephritis (PRGN, FSGN) Cystic renal diz (children and adult) |
|
Prescence of glycated squamous epitheliam in the trigone on a female's bladder is normal or abdnormal?
|
It is normal, not metaplastic
|
|
Doubl ureters drain through different orifices into the bladder T/F
|
False
|
|
Ureteral junction usually occurs in children or adults? More common in boys/girls? which side?
|
Children.
Common in boys, left side. |
|
Most common cause of hydronephrosis in infants and children
|
Ureteropelvic junction obstruction.
|
|
UPJ obstruction in adults is more common males/females? Often unilateral or bilateral?
|
Females,
Unilateral |
|
Fibroepithelial polyps and leomyoma are common benign tumor in the?
|
ureter, but may occur in renal pelvis, bladder, and urethra
|
|
Suprapubic pain, dysuria, frequency, hematuria w/ no evidence of infection in female, what is the dx
|
Hunner's Ulcer (Intersitial cystitis)
|
|
Most common bladder malignant sarcoma in children.
In adult? |
Embryono rhabdomyosarcoma..
Leomyosarcoma |
|
Most common benign mesenchymal tumor in children is?
|
Leomyoma
|
|
Polypid cystitis is most common caused by?
This looks like what kind of tumor histologically and grossly? |
Catheters.
Looks like papillary urothelial carcinoma |
|
Cystitis cystic et glandularis that have extensive intestinal metaplasia have high hisk for developing adenocarcinoma T/F
|
False.
|
|
Carcinoma insitu is high or low grade?
|
High
|
|
Urothelial papilloma
Urothelial neoplasm of low malignant potential Papillary urothelial carcinoma- low grade Papillary urothelial carcinoma - high grade. Which is least malignant? highest? |
Urothelial papilloma
Papillary urothelial carcinoma-high grade |
|
Urothelial tumors have a tendency to develop new tumors even after excision. T/F
|
True
|
|
Cystic renal dysplasia is caused by
|
abnormal metanephric differentiation.
-persistence of abnormal structure -cartilage -undifferentiated mesenchym -immature collecting tubules -abnormal lobar organizations |
|
AD polycystic kidney is bilateral or unilateral?
PKD1 and PKD2 are on which chromosomes? |
Bilateral
PKD1=16, PKD2=4 |
|
Polycystin-1 (PKD1) is involved in?
Polycystin-2 (PKD2) involves in |
Cell to cell-matrix interactions.
It is an integral membrane protein and acts as a Ca+ cation channel. |
|
Why do the cysts in ADPKD look irregular?
|
The cysts come from tubules from throughout the nephrons so they have variable lining epithelia
|
|
Are the polycysts liver in (ADPKD) asymtomatic or asymptomatic?
|
usually asymptomatic
|
|
How do ADPKD end up dying?
|
about 40% of adult patients die of coronary or hypertensive heart disease, 25% of
infection, 15% of a ruptured berry aneurysm or hypertensive intracerebral hemorrhage |
|
AR PKD is linked to what gene on what chromosome?
What is the gene product? and what does it do? |
PKHD1 on chromosome 6
Fibrocystin-may be a cell surface receptor in the collecting biliary differentiation |
|
AR PKD children who survive infancy end up with what condition?
|
Liver fibrosis
|
|
in ARPKD, how are the cyst oriented?
|
Dilated elongated channels are present at right angles to the cortical surface,
completely replacing the medulla and cortex |
|
In Medulary Sponge Kidney, the cysts arise from?
Are renal function normal or abnormal? |
The collecting ducts in the medulla.
Normal renal function. |
|
Nephronophthisis-Medullary Cystic Disease Complex have onset during adulthood or childhood
|
Childhood
|
|
In Nephronophthisis-Medullary Cystic Disease Complex, where are the cysts commonly located?
|
at the corticomedullary junction
|
|
In Nephronophthisis-Medullary Cystic Disease Complex, what is the cause for the "eventual" renal insufficiency
|
Cortical tubulointerstitial damage (some call it hereditary tubulointerstitial nephritis)
|
|
What are the 4 variants from nephronophthisis-Medullary Cystic Complex? Which is most common?
|
1)Sporadic nonfamilial(20%)
2)familial juvenile nephronopthisis (40-50) 3)Renal Retina Dysplasia (15%)- AR 4) Adult onset medullary cystic disease (AD) 4) |
|
What is the most common genetic cause of end stage renal dz in children and young adults?
|
Nephronophthisis-Medullary Cystic Disease Complex
|
|
What are the 5 related genes in Nephronophthisis-Medullary Cystic Disease Complex
|
NPH1, 2, %3 = autosomal recessive juvenile form
MCKD1, &2 = autosomal dominant, identified as causing medullary cystic disease that is characterized by progression to endstage kidney disease in adult life |
|
A children or adolescents with otherwise unexplained chronic renal failure, a positive family history, and chronic tubulointerstitial nephritis on biopsy comes in, what you should consider in your differentials?
|
Nephronophthisis-Medullary Cystic Complex
|
|
How does Nephronophthisis-Medullary Cystic Complex look grossly?
|
Kidney with cysts in the medulla at the Corticomedullary Junction, no cysts on the cortex. Glomerular structure is preserved.
|
|
The cysts in acquired (dialysis) cystic dz usually contain what?
Are they asymtomatic or symtomatic? |
Clear fluid and CALCIUM OXALATE.
Most are symtomatic |
|
Acquired (dialysis) cystic dz patients are predisposed to what?
|
Renal Cell Carcinoma of the cyst walls
|
|
Patients with tuberous sclerosis, a disease characterized by lesions of the cerebral cortex that produce epilepsy and mental retardation as well
as a variety of skin abnormalities are predisposed to what benign tumor of the kidney? |
Angiomyolipoma (vessel,smooth muscle, fat)
|
|
Name 3 benign tumor of the kidney.
|
Renal fibroma or hamartoma
Angiomyolipoma Oncocytoma |
|
Hypernephroma is the same as
|
renal cell carcinoma
|
|
Renal cell carcinoma arise from?
What is the most common risk factor? |
Tubular epithelium.
Tobacco smoking. Others are obesity, HTN, estrogen therapy, asbestos, petroleum, heavy metals. |
|
Renal cell carcinoma are related to what protooncotene? (not 100%)
|
VHL
|
|
Most common type of renal cell carcinoma.
What is the chromosomal event here? |
Clear cell carcinoma (70-80%)
Loss of short arm of chromosome 3. |
|
The 4 types of renal cell carcinoma.
Which is the hereditary form? TRisomy 7 |
Clear Cell carcinoma-3p deletion
Papillary carcinoma - related to trisomy 16,17, Y..Related to MET gene Chromophobe renal carcinoma-prominent cell membrane, pale eosinophillic w/ halo around nucleas. Multiple chromosome loss and hypoploidy Collecting duct (bellini duct) carcinoma- least common |
|
most common type of renal cancer in patients who develop dialysis-associated cystic disease
|
Papillary carcinoma
|
|
What tumor likes to invade vena cava and end up in the right said of the heart?
|
Renal cell carcinoma
|
|
These tumor cells have a rounded or polygonal shape and abundant clear or granular cytoplasm;
|
Clear cell carcinoma
|
|
Three diagnostic features for renal cell carcinoma.
Which is most reliabl? |
Costovertebral pain, hematuria, flank mass
Hematuria |
|
T/F: renal cell carcinoma tend to metatasize widely before they give rise to any local symptoms
|
True
|
|
Which bug has protein II
|
Neisseria gonorrhea
|
|
You see psommoma bodies in?
|
Papillary Carcinoma (Trisomy 7 related)
|
|
do chromophobe renal carcinoma have good or bad prognosis?
|
goood
|
|
Kidneys in nephronophthesis are small or large?
Describe the basement membranes. |
small
thickened in prox and dist tubules with interstitial fibrosis |
|
In diminished renal reserve, how are GFR, BUN, Crt.
Symtopmatic? |
GFR=50%, BUN,crt normal. Asymptomatic.
Can develop azotemia w/ more insult. |
|
GFR in renal insufficiency
|
20-50%
|
|
cystic renal dyplasia is associated with what conditions?
|
UPJ obstruction, ureteral agenesis.
|
|
If a patient comes in with multicystic kidney unilaterally. Is it PKD? what is it?
|
It's Polycystic dysplasia
|
|
ocular motor abnormalities, retinitis pigmentosa, liver fibrosis, and cerebellar abnormalities are associated with?
|
Nephronopthisis complex
|
|
Morphology of acute pyelonephritis
|
patchy intersititial suppurative inflammation
|
|
Pus the in pelvis, calyces, and ureter is known as?
|
Pyonephrosis
|
|
Aristolochic acid?
|
Chinese erbal nephropathy
|
|
Carbonic anhydrase inhibitor acts where?
|
Proximal Convoluted Tubules
|
|
When do you use a loop diuretic?
|
Emergency or Chrx edematous states (CHF, renal failure)
Also for quick fix of hypercalcemia |
|
Why does furosamide require intact kidney?
This is why you don't have furosamid with NSAIDS |
so it can produce appropriate prostiglandins to keep the kidney from ischemia and produce it's vasodialation effect to help CHF.
|
|
Hobnail pattern?
|
collecting duct carcinoma
|
|
Patient on ergot deriv and b blocker and has lymphoma, what is the predisposition?
|
Sclerosing Retroperitoneal Fibrosis
|
|
Oncocytoma is often mistaken for?
|
Chromophobe renal carcinoma
|
|
What is ormond dz?
|
Sclerosing retroperitoneal fibrosis
|
|
T/F all adenomas need treatment until benignity is confirmed?
|
true
|
|
Ultrastructure of oncocytoma.
|
Large eosinophil cell filled with mitochondria
|
|
Renal cell carcinomas come from what cell? This is the reason why it is called Renal adenocarcinoma
|
Tubular epithelium
|
|
Clear cell carcinomas are 95% sporadic (true/f)
|
True
|
|
The VHL gene encodes a protein that is part of a
ubiquitin ligase complex involved in targeting other proteins for degradation. |
That was just a fac tto know
|
|
Papillary carcinoma (familial) is on what chromosome? and what gene is turned on?
|
Chromome 7, MET (protooncogene) is turned on
|
|
Chromophobe carcinoma- chromosomes? diploidy?
|
Many chromosomal losses and extremely hypodiploidy
|
|
Renal cell carcinoma mostly affect which pole of the kiddey?
|
Upper pole
|
|
Mech of nonbacterial thrombotic endocarditis.
Risk factor? What pt get it? |
depo of small fibrin, platelets and other blood componenets on leaflet of cardiac valves-vegetations are sterile, no organism
Endocardial trauma -Catheter debilitated pts (cancer or sepsis) |
|
pathophysiology?
|
frequently occurs w/ venous thrombosis or pulnonary embolism--> suggest common orgin w/ hyperoagulable state w/ systemic activation of blood coag such as DIC
may be related to underlying dz--cancer (mucinous adenocarcinomas of pancreas) Procoagulant effect could be part of Trousseau syndrome |
|
Morphology?
Clinical signif? |
Sterile-nondestructive, small lesion occur singly or multiply along line of closure of leaflets
can produce emboli and resultant infarcts in brain, heart |
|
Mech of infective endocarditis?
What bacteria? |
colonization of bugs on heart valves--> thrombotic vegetation-->valve desctruction
50-56% = Streptococcus Viridans 10-20% = Staph aureus (IV USERS) Remain = HACEK (haemophilus, actinobacillus, cardiobacterium, Eikenella, Kingella) **in oral cavity |
|
Condition the predisposed to infective endocarditis?
|
-seeding of blood w/ microbes
-valve deformities (myxomatous valve, degenerative calcific valvular stenosis, bicuspid aortic valve, artificial valve) -neutropenia, immunodef, malignancy, diabetes, alcohol & IV use. |
|
Pathophys for acute endocardititis?
Subacute endocarditis? What does danger of the septic emboli? |
destructive tumultous infection, us. of a previously normal heart valve --50% death in days even w/ antibiotics
organism of low virulence cause infection in previously abnormal heart (go away in wks or month) it can go up and infarct the brain |
|
What valves are most commonly affected?
Which valves are more affected in IV users? How is fungal endocarditis different? |
Aortic and mitral
Right heart valves Larger vegetation than bact infection |
|
What do you see in subacute case?
What is the DUKE critia for dx infective endocarditis? |
Granulation tissue at the base (chronicity)--> fibrosis, calcification
Presence of microbe| valvular lesion| pos blood culture| echocardiogram| new valv regurge| predisposing heart lesion| fever| Vascular lesions (microemboli)| immuno phenomenon |
|
What is the immunologic phenomenon?
|
Glomerulonephritis due to immune complex trapping in kidney.
Subcutaneous nodules in pulp of digits (osler nodes) Retinal hemorrhage (Roth spots) |
|
What are the clinical finds other than microemboli?
What is Janeway lesions? ***Give prophylactic antibiotic to people with cardiac problem or artificial valve before surgica (dental) procedures |
petechia; red streaks in nail bed of digits (splinter or subungual hemorrhages);
erythematous or hemorrhage nontender lesion on plams or soles |
|
Libman Sacks endocarditis is assc with?
Which valves affected? Morphology? |
SLE (antiphospholipid)
Mitral and tricuspid vlave w/ small sterile vegetations -small, single or multiple, sterile granular pink vegetations -lesion can be on undersurface of AV, on valve endocardium, on cords or walls of atria and ventricle -Histo=finely granular, fibrinous eosinophillic material that may contain hematoxylin bodies |
|
Which valves are involved in carcinoid Heart dz?
Caused by? Why is it right sided? **If the tumor is outside of the portal system you can get right sided sydrome...if in the hepatic portal, you won't see because liver neutralize serotonin first. |
Right heart valve and endocardium
Carcinoid tumors (pancreas?) Serotonin and bradykinin are inactivated during by monoamine oxidase in lung --> no change to go to left side (check/ with pt..descrepency here) |
|
WHen do you see left sided carcinoid?
What lab values to check for? What are all the bioactive prodcts? |
pulmonary carcinoid patent foramen ovale
Serotonin, urinary excretion of 5-hydroxyindoleacetic acid (serotonin metab)--> severity of RH lesion Serotonin, kallikrein, bradykinin, histamine, prostaglandin, tachykinins |
|
What are the complications of artificial valves?
|
Thromoboembolic complications - obstuction of prosthesis by thrombus (MAJOR problem)--give anti coag med
Infective endocarditis- rare (step epidermitis, staph aureus) Structural deteriorate - uncommon cause of mechanical valve failure ; MAJOR cause for bioprothetic valve |
|
What is cardiomyopathies?
Familial/genetic relation? How to dx? |
Dz who cause is intrinsic to the myocardium
Yes, 20-35% Endomyocardial biopsy |
|
Cardiomyopathies are assc with?
What is myxedema heart? |
-infections- coxsacchie B, chlamydia, rickettsia
-Toxins: EtOH, cobalt, catecholamines, CO, lithium, hydrocarbons, arsenic, cyclophosphamide Metabolic discorders: Hyperthyroid = tachycardia Hypothyroid - long circulation Hemochromatosis -flabby enlarge, dilated due to myofiber swelling w/ loss of striations --accmpn by mucopolysaccharide rich edema fluid |
|
More asscs?
Autosomal dominant famility transthyretin amyloidosis? |
-Neuromuscular disease = Friedreich ataxia, muscular dystrophy
-Storage disorders: hunter hurler sx, glycogen storage dz, Fabry dz, amyloidosis -Leukemia, carcinoimatosis, sarcoidosis, radiation induced 4% of african have isoleucine substituted for valine at pos 122 |
|
Young athletes are susceptible to what?
|
Hypertrophy cardiomyopathy
|