Professional Documents
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BSMLS-3-Y1-3
1. Differentiate among renal diseases of glomerular, tubular, interstitial, and vascular origin.
Glomerular Disorders Immunologic issues are the main cause of most glomerular diseases.
including the kidney, the entire body. Immune complexes, such as immunoglobulin A (IgA),
circulate in the bloodstream and are deposited on the glomerular membranes because of
immunologic responses and elevated serum immunoglobulin levels. Tubular Disorders Renal
tubule-related conditions include those in which When tubules are physically damaged or when
the complex activities of the tubules are impacted by a metabolic or genetic problem, tubular
function is interrupted. Interstitial Disorders Considering the proximity of the renal diseases
affecting the renal interstitial and tubules the tubules are also impacted by the interstitial, leading
to the illness referred to as tubulointerstitial sickness. In most cases, these illnesses are
accompanied by inflammation and infections.
2. Describe the processes by which immunologic damage is caused to the glomerular
basement membrane.
A kidney-harming medicine or an infection are both potential causes of glomerular disease. In
other instances, a whole-body illness like diabetes or lupus may be at blame. The glomerulus may
expand (inflame), become inflamed (inflammation), or become sclerotic (sclerosis).
3. Describe the characteristic clinical symptoms, etiology, and urinalysis findings in acute
post-streptococcal and rapidly progressive glomerulonephritis, Goodpasture syndrome,
Wegener granulomatosis, and Henoch-Schönlein purpura.
Acute post-streptococcal
Etiology - Deposition of immune complexes, formed in conjunction with group A Streptococcus
infection, on the glomerular membranes
Clinical Course - Rapid onset of hematuria and edema, permanent renal damage seldom occurs
Urinalysis findings - Results are always abnormal. Hematuria and proteinuria are present in all
cases. Urine sediment has red blood cells, red blood cell casts, white blood cells, granular casts,
and, rarely, white blood cell casts
Rapidly progressive glomerulonephritis
Etiology - Deposition of immune complexes from systemic immune disorders on the
glomerular membrane
Clinical Course - Rapid onset with glomerular damage and possible progression to end-stage
renal failure
Urinalysis findings - Rapidly progressive glomerulonephritis (RPGN) is defined by the
identification of an active urinary sediment on urinalysis, including hematuria (especially with
dysmorphic red cells), red cell casts, and proteinuria (>500 mg/d) in the setting of a rising
blood urea nitrogen and serum creatinine.
Goodpasture syndrome
Etiology - Attachment of a cytotoxic antibody formed during viral respiratory infections to
glomerular and alveolar basement membranes
Clinical Course - Hemoptysis and dyspnea followed by hematuria
Urinalysis findings - are characteristic of acute glomerulonephritis, usually demonstrating low-
grade proteinuria, gross or microscopic hematuria, and red blood cell casts. On the complete
blood cell count, anemia may be observed secondary to iron deficiency caused by
intrapulmonary bleeding.
Wegener granulomatosis
GARCIA HANNA CASANDRA L.
BSMLS-3-Y1-3