AIM • KMU Exam Practice
KMU Past Paper Practice
Glomerular Diseases and Nephrotic–Nephritic Syndromes
4th Year MBBS • 20 A-type Single Best Answer MCQs • Pathology, Medicine & Pediatrics
MCQ 1
Question:
A 61-year-old man with systemic amyloidosis develops progressive ankle edema and heavy proteinuria. Renal function is initially preserved. Which pathological process most directly explains his urinary protein loss?
Options:
Selective inflammation of renal tubules
Proliferation of parietal epithelial cells
Extracellular protein deposition distorting the filtration barrier
Acute obstruction of glomerular capillary loops
Primary loss of collecting-duct water permeability
Correct Answer: Extracellular protein deposition distorting the filtration barrier
Explanation: Amyloid deposition within glomeruli disrupts the filtration barrier, allowing substantial plasma protein loss and producing a secondary nephrotic syndrome.
MCQ 2
Question:
A 54-year-old woman with long-standing diabetes mellitus has normal serum creatinine during routine follow-up. Which renal abnormality is expected to become clinically detectable earliest as diabetic glomerular injury develops?
Options:
Increasing urinary albumin excretion
Persistent red-cell cast formation
Rapid development of severe azotemia
Marked reduction in serum complement
Diffuse crescent formation in glomeruli
Correct Answer: Increasing urinary albumin excretion
Explanation: Increasing urinary albumin loss is an early clinically detectable manifestation of diabetic glomerular damage and may precede a measurable decline in filtration.
MCQ 3
Question:
A renal biopsy from a patient with persistent proteinuria shows sclerosis involving part of the tuft in several glomeruli, while many other glomeruli appear unaffected. Which interpretation of this distribution is most accurate?
Options:
All glomeruli have complete tuft involvement
Only the mesangium is affected diffusely
The lesion is limited to tubular segments
Every glomerulus has partial capillary injury
Some glomeruli are affected and only part of each involved tuft is scarred
Correct Answer: Some glomeruli are affected and only part of each involved tuft is scarred
Explanation: “Focal” means only some glomeruli are involved, while “segmental” means sclerosis affects only part of an affected glomerular tuft.
MCQ 4
Question:
A pathology report describes a membranoproliferative pattern of glomerular injury. The treating physician requests further etiological evaluation rather than considering the biopsy label a complete diagnosis. Which statement best explains this approach?
Options:
The pattern occurs only after streptococcal infection
The pattern can result from different immune-complex or complement-mediated mechanisms
The pattern represents isolated podocyte dysfunction
The pattern is confined to diabetic nephropathy
The pattern indicates a purely tubular disorder
Correct Answer: The pattern can result from different immune-complex or complement-mediated mechanisms
Explanation: MPGN is a morphological pattern rather than one single disease, so identifying the underlying immune-complex or complement mechanism is important.
MCQ 5
Question:
A 27-year-old man with acute glomerulonephritis develops facial edema and hypertension. His serum albumin is only mildly reduced. Which mechanism best explains the edema and raised blood pressure?
Options:
Marked hepatic albumin suppression
Loss of plasma lipoproteins into urine
Increased renal glucose reabsorption
Renal sodium and water retention from reduced filtration
Reduced production of inflammatory mediators
Correct Answer: Renal sodium and water retention from reduced filtration
Explanation: In nephritic disease, reduced GFR promotes sodium and water retention, causing extracellular volume expansion, edema and hypertension.
MCQ 6
Question:
A glomerular biopsy from a patient with active inflammatory glomerulonephritis shows numerous neutrophils and monocytes within capillary loops. How do these cells contribute to glomerular injury?
Options:
They increase synthesis of plasma albumin
They release enzymes and oxidants that damage capillary walls
They reduce mesangial matrix production
They restore podocyte slit diaphragms
They increase tubular protein reabsorption
Correct Answer: They release enzymes and oxidants that damage capillary walls
Explanation: Activated inflammatory cells release proteolytic enzymes, oxidants and other mediators that amplify immune-mediated glomerular capillary injury.
MCQ 7
Question:
A 21-year-old man with recurrent glomerular hematuria undergoes biopsy. Immunoglobulin-containing deposits are concentrated in the mesangium. Which tissue response is most likely to accompany this deposit location?
Options:
Complete disappearance of glomerular cells
Selective necrosis of collecting ducts
Isolated thickening of renal arteries
Loss of all glomerular endothelial fenestrations
Mesangial-cell proliferation with increased matrix
Correct Answer: Mesangial-cell proliferation with increased matrix
Explanation: Mesangial immune deposits activate mesangial cells, producing proliferation and increased extracellular matrix within the glomerulus.
MCQ 8
Question:
A patient with poorly controlled diabetes develops progressive mesangial expansion and glomerular basement-membrane thickening. Which combination best explains the development of these structural changes?
Options:
Non-enzymatic glycation with chronic glomerular hemodynamic stress
Acute bacterial invasion with neutrophil destruction
Isolated IgA deposition with complement preservation
Sudden loss of all functioning podocytes
Transient reduction of renal plasma flow alone
Correct Answer: Non-enzymatic glycation with chronic glomerular hemodynamic stress
Explanation: Chronic hyperglycemia alters matrix proteins through glycation, while glomerular hemodynamic stress promotes further matrix production and sclerosis.
MCQ 9
Question:
A 30-year-old woman with systemic lupus erythematosus develops hematuria, proteinuria and edema. Her renal biopsy demonstrates immune deposits at more than one glomerular site. Why can this systemic disease produce either nephritic, nephrotic or mixed renal presentations?
Options:
It selectively injures only renal tubular cells
It produces a fixed lesion in every patient
Immune deposits can affect different glomerular compartments and patterns of injury
It causes protein loss without glomerular structural damage
Its renal effects are limited to collecting ducts
Correct Answer: Immune deposits can affect different glomerular compartments and patterns of injury
Explanation: Lupus can produce immune-complex deposition in different glomerular locations, creating variable inflammatory and permeability defects and therefore different clinical syndromes.
MCQ 10
Question:
An 8-year-old child develops dark urine, facial swelling and reduced urine output after a recent streptococcal infection. If renal tissue were examined during the acute illness, which light-microscopic pattern would best fit the disease process?
Options:
Normal glomeruli without cellular change
Focal segmental areas of sclerosis only
Diffuse nodular mesangial sclerosis
Diffuse glomerular hypercellularity with inflammatory-cell infiltration
Isolated tubular epithelial necrosis
Correct Answer: Diffuse glomerular hypercellularity with inflammatory-cell infiltration
Explanation: APSGN produces a diffuse proliferative glomerulonephritis with increased glomerular cellularity and inflammatory-cell infiltration.
MCQ 11
Question:
A child presents with acute post-streptococcal glomerulonephritis after the preceding throat infection has already resolved. Which management approach best reflects the pathogenesis of the renal disease?
Options:
Provide supportive renal care and treat any persisting streptococcal infection
Treat the kidney as a site of continuing bacterial invasion
Use prolonged antimicrobial therapy as the sole renal treatment
Increase sodium intake to improve renal perfusion
Begin routine anticoagulation for all affected children
Correct Answer: Provide supportive renal care and treat any persisting streptococcal infection
Explanation: The nephritis is immune mediated rather than due to direct renal infection, so management is mainly supportive while any ongoing streptococcal infection is appropriately treated.
MCQ 12
Question:
The parents of a 9-year-old child recovering from uncomplicated acute post-streptococcal glomerulonephritis ask about the expected renal outcome. Which statement is most appropriate?
Options:
Most children progress rapidly to end-stage renal disease
Persistent nephrotic syndrome is the expected outcome
Long-term dialysis is routinely required
Progressive FSGS commonly follows the acute episode
Most children recover renal function well
Correct Answer: Most children recover renal function well
Explanation: The renal prognosis of uncomplicated APSGN in children is generally favorable, although severe acute complications still require careful monitoring.
MCQ 13
Question:
A 6-year-old child with marked nephrotic edema becomes lethargic and develops tachycardia with cool extremities. Despite generalized swelling, which complication should be considered?
Options:
Acute complement excess
Intravascular volume depletion
Primary erythrocytosis
Excess glomerular filtration
Isolated tubular alkalosis
Correct Answer: Intravascular volume depletion
Explanation: Severe nephrotic edema can coexist with reduced effective circulating volume because fluid has shifted from the vascular compartment into interstitial tissues.
MCQ 14
Question:
An 8-year-old child with initially steroid-sensitive nephrotic syndrome develops repeated relapses requiring several courses of corticosteroids and begins to show treatment-related toxicity. Which management principle is most appropriate?
Options:
Stop follow-up because the kidneys are permanently protected
Treat future relapses only with increased dietary protein
Arrange specialist review for steroid-sparing or alternative immunomodulatory therapy
Assume each relapse represents acute bacterial glomerulonephritis
Proceed directly to long-term renal replacement therapy
Correct Answer: Arrange specialist review for steroid-sparing or alternative immunomodulatory therapy
Explanation: Frequent relapses, steroid dependence or significant steroid toxicity warrant specialist reassessment and consideration of alternative immunomodulatory treatment.
MCQ 15
Question:
A 39-year-old man with nephrotic syndrome has marked hyperlipidemia despite no previous lipid disorder. Which physiological response most directly contributes to this abnormality?
Options:
Reduced filtration of circulating lipids
Decreased renal production of erythropoietin
Reduced hepatic synthesis of plasma proteins
Increased hepatic lipoprotein synthesis
Increased glomerular erythrocyte permeability
Correct Answer: Increased hepatic lipoprotein synthesis
Explanation: In nephrotic syndrome, the liver responds to plasma protein loss by increasing synthesis of proteins and lipoproteins, contributing to hyperlipidemia.
MCQ 16
Question:
A 57-year-old woman presents with nephrotic syndrome. Biopsy demonstrates a membranous pattern. Her physician reviews her history for systemic autoimmune disease, chronic infection, drug exposure and malignancy. What is the main reason for this additional assessment?
Options:
Membranous disease is caused only by diabetes mellitus
Systemic conditions affect only the renal tubules
The biopsy pattern excludes secondary disease
Secondary causes produce only a nephritic syndrome
A membranous pattern may occur secondary to systemic disease or exposure
Correct Answer: A membranous pattern may occur secondary to systemic disease or exposure
Explanation: Membranous nephropathy may be primary or secondary, so relevant systemic diseases, infections, drugs and malignancy should be considered.
MCQ 17
Question:
A 46-year-old patient with severe nephritic syndrome develops worsening renal failure and pulmonary edema despite appropriate medical treatment. A major electrolyte disturbance also develops. Which management principle should now be considered?
Options:
Renal replacement therapy for severe complications of renal failure
Routine corticosteroids without determining the cause
Increased dietary sodium and fluid intake
Observation alone until the creatinine normalizes
Lipid-lowering treatment as the immediate priority
Correct Answer: Renal replacement therapy for severe complications of renal failure
Explanation: Refractory fluid overload or major electrolyte disturbances in severe acute renal failure are indications to consider renal replacement therapy.
MCQ 18
Question:
A renal biopsy from a patient with rapidly deteriorating renal function shows crescents in many glomeruli. The clinical team is asked to interpret the pathological significance before further cause-directed testing. Which interpretation is most accurate?
Options:
Crescents identify one specific infectious disease
Crescents are characteristic of uncomplicated nephrotic syndrome
Crescents indicate severe glomerular injury but do not define a single cause
Crescents demonstrate isolated tubular obstruction
Crescents confirm diabetic nephropathy
Correct Answer: Crescents indicate severe glomerular injury but do not define a single cause
Explanation: Crescent formation is a morphological marker of severe capillary-wall injury; the underlying immune or inflammatory cause must still be determined.
MCQ 19
Question:
A 10-year-old child develops an acute nephritic syndrome after a recently documented streptococcal skin infection. Which additional investigation would most directly support the suspected preceding infectious trigger?
Options:
Serum lipid profile alone
Appropriate serological evidence of recent streptococcal infection
Urinary ketone measurement
Serum calcium measurement
Bleeding-time assessment
Correct Answer: Appropriate serological evidence of recent streptococcal infection
Explanation: In suspected APSGN, evidence of a preceding streptococcal infection supports the etiological link when interpreted with the clinical and renal findings.
MCQ 20
Question:
A 44-year-old patient with nephrotic syndrome has heavy proteinuria and hyperlipidemia. Urine microscopy also demonstrates lipid-containing material. Which process best explains the appearance of lipids in the urine?
Options:
Destruction of erythrocytes within Bowman space
Reduced hepatic synthesis of circulating lipids
Bacterial production of lipids inside renal tubules
Passage of circulating lipoproteins through an abnormal filtration barrier
Failure of glomeruli to filter plasma water
Correct Answer: Passage of circulating lipoproteins through an abnormal filtration barrier
Explanation: Severe glomerular permeability dysfunction allows lipoprotein-containing material to enter the filtrate, producing the characteristic lipiduria of nephrotic syndrome.