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Tubulointerstitial Diseases of the Kidney

Tubulointerstitial Diseases of the Kidney. Pelvis, Cortex, medulla, calyces Renal Artery. 1700 L of blood filtered  180 L of G lomerul filtrate  1.5 L of urine / day. Diseases affecting tubules & interstitium:.

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Tubulointerstitial Diseases of the Kidney

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  1. Tubulointerstitial Diseases of the Kidney

  2. Pelvis, Cortex, medulla, calyces • Renal Artery

  3. 1700 L of blood filtered  180 L of Glomerul filtrate  1.5 L of urine / day.

  4. Diseases affecting tubules & interstitium: 1-Ischemic or toxic tubular injury leading to acute tubular necrosis (ATN) and Acute Renal Failure (ARF) 2-Inflammatory reactions of tubules and interstitium (tubulointerstitial nephritis) • Infections (Acute & Chronic pyelonephritis...) • Toxins (Drugs, analgesic nephritis, Heavy metals, lead, cadmium) • Physical Factors (Chronic urinary tract obstruction, radiation nephritis) • Neoplasms (Multiple myeloma) • Immunologic reactions (Transplant rejection, Sjögren Syndrome) • Metabolic diseases (Urate & oxalate nephropathy, nephrocalcinosis, hypokalemic nephropathy...) • Vascular diseases • Miscellaneous (Balkan nephropathy, idiopathic interstitial nephritis...)

  5. ACUTE TUBULAR NECROSIS ATN; acute renal failure, renal shutdown ATN is a clinicopathologic entity characterized by destruction of tubular epithelial cells and clinically by acute supression of renal functions. It is the most common cause of renal failure. Acute supression of renal function and urine flow falling within 24 hours to less than 400 ml.

  6. Causes of ATN: 1-Organic vascular obstruction. 2-Severe glomerular disease 3-Acute tubulointerstitial nephritis. 4-Massive infection 5-DIC 6-Urinary obstruction by tumors, BPH, or blood-cloths

  7. Ischemic ATN • Hypovolemic shock, • massive hemorrhage, • septic shock, • burns, • prolonged surgical operations. • New transplants, • Contrast media (radiology), • Non-steroidal anti-inflammatory agents, • ACE-inhibitor drugs.

  8. Nephrotoxic ATN • Renal poisons (nephrotoxins) • heavy metals (mercury), • toxic chemicals (carbon tetrachloride, ethylene glycol), • drugs (cisplatin) • poisons (Amanita phalloides). • Viral hemorrhagic fevers • often cause temporary renal shutdown. • Heme proteins (Pigment nephropathy) • Myoglobin (rhabdomyolysis) • Hemoglobin (hemolysis)

  9. (Pigment nephropathy) Massive hemolysis (red cell stroma plugs the tubules) • ABO mismatch, • falciparum malaria, • Snake bite. • Massive rhabdomyolysis (myoglobin and other muscle debris plugs the tubules) • crush injury, • lightning, • cocaine, • torture

  10. The pathophysiology of ATN is complex • Ischemia and nephrotoxins directly damage tubules (Free radical and endothelin as mediators). • Systemic hypotension and severe poisoning also cause intrarenal vasoconstriction, which compounds ischemic damage and lowers GFR (Glomerular Filtration Rate). • Damaged tubules become obstructed by casts and crud, which further lowers GFR. • Direct glomerular damage may occur (especially in DIC) • Tubular backleak contributes to oliguria.

  11. Clinical Aspectsof ATN • The most common cause of acute renal failure • “Dirty” brown casts in urine • Oliguria anuria polyuria • Azotemia • Acidosis, K • Fluid retention • Recovery 1-2 weeks

  12. The histology (reflects the pathophysiology): • Ischemic ATN: • A few necrotic cells or denuded basement membrane, • Dilated tubules • Interstitial edema • Regeneration of proximal tubular cells (basophilic cytoplasm, active nuclei, maybe even a mitosis or two). • Electron micrographs show disruption of the brush borders. • Nephrotoxic ATN: • frank necrosis (usually limited to the proximal tubules) • without rupture of basement membranes.

  13. ATN

  14. Other causes of acute renal shutdown, other than ATN: • Renal causes • atheroembolization (very common) • drug hypersensitivity (very common) • hepatorenal syndrome (very common) • severe rapidly-progressive glomerulonephritis • vasculopathies (polyarteritis nodosa, malignant hypertension, scleroderma, hemolytic-uremic syndrome) • severe pyelonephritis (especially with papillary necrosis) • DIC-diffuse renal cortical necrosis • acute urate nephropathy • Prerenal causes • dehydration, • shock, • congestive heart failure. • Postrenal causes • urinary tract obstruction (tumors, blood clots, prostate trouble).

  15. HEPATORENAL SYNDROME • Kidney failure that develops in patients with liver failure, without anatomic changes in the kidney • except perhaps bile-staining of hyaline casts • Common cause: administration of high-powered diuretics (Lasix) to a cirrhotic. • Liver failure from any cause produces hypotension, and "hepatorenal syndrome" may also have a component of "shock kidney" (acute tubular necrosis).

  16. UPPER URINARY TRACT INFECTIONS

  17. An extremely common, serious problem in clinical medicine. • Causes: • Ascending infection (80%) • E. coli and other gram-negatives, swimming upstream from bladder infections, common • Hematogenous infection • especially staph. and Tbc., uncommon

  18. Acute pyelonephritis • Predisposing conditions • bacterial virulence • patient's sex and age (up to 40, females predominant; over 40, males predominant) • urinary obstruction and/or stasis (Prostatic hyperplasia) • vesicoureteral reflux (malformed or damaged ureterovesical "valve") • mechanical factors (iatrogenic instrumentation, "honeymoon cystitis"); pregnancy (ureteral dilatation due to hormones) • asymptomatic bacteriuria (small % of females of any age) • pre-existing renal diseases (especially kidney stones) • diabetes mellitus • not being circumcised (little boys; impressive risk) • public bathroom • not drinking enough water.

  19. Histological: • PMNL's infiltrate the interstitium and tubules (even 1-2 PMNLs in tubules), • Abscesses with tissue destruction. • Clinical: • fever, • pain at costovertebral angle, • PMN's and white cell casts in the urine. • Papillary necrosis is a dreaded complication of pyelonephritis that occurs mostly in diabetics. • Beethoven had papillary necrosis for some reason?

  20. Acute pyelonephritis

  21. Other forms of Acute interstitial nephritis • Autoimmune dieseases • anti-TBM antibody • Polyomavirus infection • in the immunosuppressed • especially kidney transplant patients • decoy cells (with huge basophilic inclusions)

  22. Polyomavirus infection

  23. Chronic pyelonephritis and reflux nephropathy • Pyelonephritis always produces some renal scarring around the calyces and pelvis and among the tubules. • Destruction of renal tissue and fibrosis • Cortical scars • Loss of papillae • Ectasia of calices • Hydronephrosis.  Irregularly shrunken small kidney.

  24. Microscopically: • Patchy process with periglomerular fibrosis (outside Bowman's capsule) • Interstitial scarring • Scar retraction produces dilatation of cast-filled tubules, or "thyroidization").

  25. Chronic pyelonephritis

  26. End-stage kidney

  27. The clinical picture varies: • acute recurrent pyelonephritis • probably the patient has a urinary tract malformation • insidious onset of renal insufficiency and hypertension • Note that chronic pyelonephritis is an extremely important cause of morbidity and mortality in the wheelchair-bound.

  28. Xanthogranulomatous pyelonephritis • a special, common type of chronic pyelonephritis • older women who have had several episodes of acute pyelonephritis. • Lipid-laden macrophages form large yellow nodules that look very much like renal cell carcinoma, both grossly and microscopically. • Causes: • Proteus infection • a stone • Located mostly around the pelvis • the process tends to spread, and it can grow out around the kidney and may erode into the area around the kidney • produce fistulas to the groin, back, or gut.

  29. CHRONIC INTERSTITIAL NEPHRITIS • CIN is scarring of the kidney from some process that is primarily interstitial • not some glomerular or vascular disease • Causes: • Lupus (peritubular immune deposits) • Sjögren's syndrome (often include an acute or chronic interstitial nephritis) • AIDS • Granulomatous CIN is due to drugs or sarcoid.

  30. (DRUG INDUCED RENALDISEASES) • Acute tubulointerstitial nephritis (allergic) • Analgesic nepropathy (phenacetin) • Acute tubular necrosis(toxic).

  31. 1. Acute tubulointerstitial nephritis • Hypersensitivity • Within a month after drug exposure, the victim develops fever, skin rash eosinophilia, hematuria, proteinuria, sterile pyuria and eosinophiliuria. Withdrawal of drugs makes things better. • Histology: • edema, and interstitial mononuclear cell infiltration, • eosinophils and neutrophils may be found. • Causes: • Methicillin (best-known), Sulfa drugs, rifampin, cyclosporine, penicillin, furosemide ("Lasix"), thiazides.

  32. 2. Analgesic nephritis • Analgesic abuse nephropathy • Phenacetin-containing combinations for pain. • Chronic interstitial inflammation is characteristic, and many patients develop papillary necrosis. • Transitional cell carcinoma of renal pelvis may also result from patients who overdid phenacetin (10% of abusers).

  33. Analgesic nephropathy

  34. Classic non-steroidal anti-inflammatory agents • This very useful class of drugs (arthritis, menstrual cramps, etc.) is also today's most common cause of renal shutdown in outpatients. • The prognosis is generally excellent when the drug is withdrawn. • Examples: • Fenprofen nephropathy: a combination of minimal-change glomerulopathy ("foot process disease") histology with nephritic and/or nephrotic syndrome, plus marked chronic interstitial nephritis.

  35. 3. Acute tubular necrosis(toxic) Poisons (Nephrotoxic agents) • Lead, • Cadmium (the Japanese pollution nightmare) • Bismuth (interstitial nephritis, acid-fast "Cowdry A" inclusions in the proximal tubules, Fanconi syndrome), • Amanita phalloides, • Carbon tetrachloride (fatty change).

  36. METABOLIC TUBULAR INJURY • Hypercalcemia • uric acid stones • Hypercalciuria • Nephrocalcinosis • Calcium stones. • Hyperuricemia (gout) • urate nephropathy

  37. HYPERCALCEMIC NEPHROPATHY • Extensive metastatic calcification of the kidney tubules (nephrocalcinosis) • chronic inflammation or obstruction • because the ascending limb of Henle's loop is damaged first, one early problem is inability to concentrate urine. • Even in the absence of tubular calcification, hypercalcemia produces a prerenal azotemia by causing constriction of the small renal arteries.

  38. Primary (increased intestinal absorption of Calcium) Idiopathic (common) Milk-alkali syndrome Vitamin D excess Sarcoidosis Secondary (release of Calcium from bones) Renal osteodystrophy Hyperparathyroidism Osteolytic metastases (e.g. breast cancer) Paraneoplastic syndromes (PTrP) CAUSES ofHYPERCALCEMIA & HYPERCALCIURIA

  39. Nephrocalcinosis

  40. HYPOKALEMIC NEPHROPATHY • When serum potassium is low, the kidney cannot concentrate urine. • Coarse vacuolization of tubular cells, dilatation of intercellular spaces.

  41. PLASMA CELL MYELOMA KIDNEY • Precipitation of Bence-Jones protein within the tubules causing renal shutdown. • Patients experience the acute or insidious onset of renal failure. • Amorphous pink casts, often surrounded by a foreign-body reaction with multinucleated giant cells. • Light-chain nephropathy can also include tubular casts. • Plasma cell myeloma patients often get amyloidosis B.

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