Renal Tubular Disease
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Contents |
More Specific Terms
- acute tubular necrosis (ATN)
- medullary sponge kidney disease
- pyelonephritis
- renal tubular acidosis (RTA)
- renal tubulointerstitial disease
Etiology
- hereditary disorders (see hereditary renal tubular defects)
- acquired disorders
Pathology
- patterns of renal tubular injury [1]
- tubular proteinuria < 1.5-2 g/day
- proximal tubule dysfunction
- distal tubule dysfunction
- hyperchloremic acidosis*
- hyperkalemia or hypokalemia
- salt wasting
- medullary concentration dysfunction
- nephrogenic diabetes insipidus with decreased urine concentrating ability
- transport dysfunction of renal tubular injury [2]
- reduced GFR*
- obliteration of vasculature
- obstruction of renal tubules
- impaired proximal tubular reabsorption of glucose, amino acids, phosphate & bicarbonate
- reduced ammonia production
- inability to acidify collecting duct fluid (distal renal tubular acidosis)
- proximal tubular bicarbonate wasting
- tubular or low-molecular weight proteinuria*
- defect is proximal tubular protein reabsorption
- K+ secretory defects
- aldosterone resistance
- salt wasting
- distal tubular damage
- failure of Na+ reabsorption
- * common
Laboratory
- urine sediment)
- urine protein (tubular proteinuria)
- aminoaciduria
- glycosuria
- serum chemistries
More General Terms
Additional Terms
References
- Mayo Internal Medicine Board Review, 1998-99, Prakash UBS (ed) Lippincott-Raven, Philadelphia, 1998
- Harrison's Principles of Internal Medicine, 13th ed. Isselbacher et al (eds), McGraw-Hill Inc. NY, 1994, pg 1314, 1324
