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Vascular diseases of Kidney1.Hypertensive Renal Disease: Nephrosclerosis-Benign
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1. Kidney
2. Vascular diseases of Kidney
1.Hypertensive Renal Disease:
Nephrosclerosis-Benign & Malignant
2.Thrombotic Microangiopathies:
Childhood & Adult Hemolytic-Uremic Syndrome (HUS)
Adult (female) Thrombotic Thrombocytopenic Purpura (TTP)
Autoimmune Diseases
Toxemia of pregnancy
Severe bacterial infections.
3.Renal Artery Stenosis (RAS):
Atherosclerotic or Fibromuscular dysplasia
reversible hypertension
4.Renal Infarcts:
Embolic or Thrombotic.
3. 1. Hypertension
Most renal diseases cause HTN
HTN has marked effects on the kidneys
Benign Nephrosclerosis= hyaline arteriosclerosis
Most are at risk for developing malignant hypertension
Malignant Nephrosclerosis= Hyperplastic arteriolosclerosis
Fibrinoid necrosis of arterioles
Thrombotic Microangiopathy (Necrotizing Glomerulitis)
? renal blood flow therefore, ? renin -angiotensin system ? ?BP ? hypertension.
Clinical:
Neurological =Disoriented ? coma
Eyes = Papilledema
Renal = proteinuria, Hematuria & RF
4. Benign Nephrosclerosis Fine leathery granularity,
5. Benign Nephrosclerosis Hyaline change in small blood vessels
6. Malignant Nephrosclerosis Hyperplastic arteriolosclerosis (onion-skinning)
Blood vessels have collagen deposits making the onion skinning appearance
Notice how lumen gets very small
7. 2. Thrombotic Microangiopathies
Common findings:
Thrombosis in small vessels
Microangiopathic hemolytic anemia (MHA)
Thrombocytopenia
Pathogenesis:
Endothelial injury ? platelet aggregation? thrombosis
Vasoconstriction ? ischemia ? necrosis
A) Childhood Hemolytic Uremic Syndrome (HUS)
E. coli (infected Hamburgers)
Clinical: renal failure is prominent
Intestinal bleeding, oliguria, Hematuria, MHA, HTN
B) TTP = young females with High mortality
8. Fibrin Thrombi (Childhood HUS) Caused by DIC, HUS (E. coli 0157H7)
9. 3. RENAL ARTERY STENOSIS (RAS)
10. Fibromuscular Dysplasia Fibromuscular dysplasia
11. 4. Renal infarcts
Branches of Renal artery - End arteries.
MCC= MI and thromboembolism from Atrial Fibrillation
Clinical:
Asymptomatic or
Large unilateral -May cause HTN
Extensive bilateral -May cause RF
12. Renal Infarcts
13. Renal Infarcts
14. Kidney
15. Tubulo – Interstitial diseases
1. Acute Tubular Necrosis (ATN)
2. Pyelonephritis (PN)
Acute
Chronic
3. Acute drug-induced Interstitial Nephritis
4. Analgesic Abuse Nephropathy
5. Metabolic Tubulointerstitial Disease
Urate
Hypercalcemia
Multiple Myeloma
16. 1. Acute Tubular Necrosis (ATN)
Most serious but reversible kidney disease,
Causes= next slide
Pathology= destruction of tubular epithelial cells ?Acute suppression of renal function, urinary output <400 ml/day
ATN ?ARF by mechanisms
Tubular cell injury? Tubulo glomerular feed back
Tubular obstruction by Hyaline or pigmented granular casts (Tamm-Horsfall proteins secreted by tubular epithelium)
Back-leak of tubular fluid into the interstitial space (due to death of tubular cells)
The outcome of all the above three is ?GFR (oliguria)
Clinical Course= Three phases
Initial phase= (first 36 hrs.), Dominated by the cause
Maintenance phase= Oliguria & acute uremia
Salt & water retention
Hyperkalemia and metabolic acidosis.
Rx – fluid & Electrolyte balance, dialysis
Recovery phase=Polyuria & electrolyte loss
Hypokalemia (give lots of fluids + K+ sparing diuretics)
?risk of infections
BUN & creatinine levels return to normal
17. ATN- Causes
18. ATN Necrotic & Regenerating tubular epithelial cells
19. 2. Pyelonephritis (PN)= Bacterial infection of kidney
Causes? chronic urinary tract infection
Routes of bacterial entry into kidneys
1.Ascending Infection (MCC)
by vesico-ureteral reflux (VUR)
2. Hematogenous Infection (septicemia)
Helped by lower UT obstruction
Pathology = Inflammation - renal parenchyma & pelvis
Clinical= asymptomatic or cause severe flank pain & fever
Lab= Bacteria, leukocytes & Casts
High risk pts= DM, pregnancy & UT obstruction
Complications = Necrotizing papillitis or papillary necrosis
(papillary necrosis is seen in 4 conditions????)
( CT scan - best investigation)
Pathologic types = Acute PN, Chronic PN
20. Acute Pyelonephritis = Neutrophilic exudate within tubules and renal substance
kidney is almost unrecognizable
Complications= papillary necrosis, Perinephric abscesses, Pyonephrosis, Scarring (Chronic Pyelonephritis)
Chronic Pyelonephritis (CPN) = Chronic tubulointerstitial inflammation
Characterized by= CRF & HTN
Pathology = corticomedullary scars overlying dilated blunted calyces.
Forms of CPN
1 Reflux nephropathy-associated type
MCC of CPN
MCC of reflux= Congenital intra-renal reflux With superimposed bacterial infection (E. coli).
2.Obstructive type
predisposes to recurrent bacterial infections (E. coli)
Course= Glomeruli undergo ischemic atrophy, total sclerosis with fine leathery granularity, shrunken.
Finally Glomeruli disappears
21. Acute Pyelonephritis Neutrophilic exudate within tubules and renal substance – kidney is almost unrecognizable
22. Chronic Pyelonephritis (CPN)
23. Chronic Pyelonephritis (CPN)
24. 3 . Acute drug-induced interstitial nephritis
Manifests 2-40 days after the start of Rx (methicillin, ampicillin, rifampicin, thiazides, NSAID, cimetidine, .... )
Clinical= Presents with fever, skin rash, hematuria, proteinuria, sterile pyuria, Eosinophilia= (allergic, parasitic and Drug reactions), azotemia, and acute RF
Pathology = Eosinophils and mononuclear infiltrates & Patchy tubular necrosis
Withdrawal of drug ? recovery
4. Analgesic Abuse Nephropathy = Chronic tubulointerstitial nephritis with papillary necrosis
Caused by= Habitual intake of large doses
Acetaminophen (Tylenol) ? directly damages cells
Aspirin -vasoconstriction ? ischemia
Pathology = papillary necrosis ( other causes???)
Clinical= Presents with Polyuria, Nocturia, HTN, headache, GI symptoms, anemia, may develop UTI, may develop CRF
Complications= ? risk for TCC (Transitional cell Carcinoma) - renal pelvis
25. Drug-induced interstitial nephritis
26. Analgesic Abuse Nephropathy Papillary necrosis
27. Analgesic Abuse Nephropathy Can slough off and obstruct urinary tract
28. 5. Metabolic Tubulointerstitial Disease
Urate Nephropathy: form of:
Acute RF (with cancer chemotherapy).
Chronic RF (with gout & chronic lead poisoning).
Hypercalcemia: cause RF by:
Nephrolithiasis (causing UT obstruction).
Nephrocalcinosis (causing renal atrophy).
Multiple Myeloma:
Acute or chronic RF
result of Bence - Jones & Tamm-Horsfall proteinuria,
Hypercalcemia & Nephrotoxic drugs
Cast nephropathy
Amyloid deposits- Light-chain nephropathy -AL
29. MULTIPLE MYELOMA (plasma cells) Note tubular casts
30. Kidney
31. OBSTRUCTIVE UROPATHY (HYDRONEPHROSIS)
Characterized by:
Unrelieved UT obstruction
Leads to renal atrophy, with dilatation of the renal pelvis and calyses ? “Hydronephrosis” – all widened due to obstruction and distension in pelvis.
Still have glomerular filtration ? increase in urine load ? distension
If Bilateral ? CRF
32. HYDRONEPHROSIS Causes are:
Congenital anomalies
(vesicoureteral reflux, urethral valves, meatal stenosis)
Urinary calculi
Benign prostatic hypertrophy
Tumors
Pregnancy
Neurogenic bladder
Inflammatory strictures (including retroperitoneal fibromatosis).
33. HYDRONEPHROSIS “Hydronephrosis” – all widened due to obstruction and distension in pelvis
34. Kidney