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PA27.8-17 | Renal Pathology II: Tubulointerstitial, Vascular & Neoplastic — Practice Quiz

Practice 14 questions · Untimed · Unlimited attempts

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Q1 PA27.8 1 pt

Which of the following best classifies the cause of acute tubular necrosis (ATN) in a patient who develops oliguria 48 hours after an emergency laparotomy for ruptured aortic aneurysm with prolonged intraoperative hypotension?

A Ischaemic ATN due to prolonged renal hypoperfusion
B Nephrotoxic ATN due to surgical anaesthetic agents
C Obstructive uropathy from post-surgical clot
D Acute interstitial nephritis from prophylactic antibiotics

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Q2 PA27.8 1 pt

A urine microscopy from a patient with oliguric ATN shows coarsely granular 'muddy-brown' casts. These casts form primarily from:

A Aggregated white blood cells shed from inflamed tubules
B Precipitated uric acid crystals within tubular lumina
C Fatty droplets from lipid-laden proximal tubular cells
D Desquamated necrotic tubular epithelial cells and their debris

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Q3 PA27.9 1 pt

A 35-year-old woman presents with high fever, rigors, right loin pain, and dysuria for 3 days. Urine culture grows Escherichia coli >10⁵ CFU/mL. Urine microscopy is most likely to show:

A Red cell casts
B White cell (pus) casts
C Muddy-brown granular casts
D Waxy casts with broad diameter

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Q4 PA27.9 1 pt

A 58-year-old diabetic man with recurrent urinary tract infections develops sudden severe right flank pain and haematuria. CT shows a wedge-shaped, hypo-enhancing area at the right renal papilla. The most likely complication is:

A Renal cortical abscess (carbuncle)
B Xanthogranulomatous pyelonephritis
C Papillary necrosis
D Perinephric haematoma

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Q5 PA27.10 1 pt

Chronic pyelonephritis (reflux nephropathy) produces a characteristic gross appearance of the kidney. Which feature best distinguishes it from hypertensive nephrosclerosis?

A Diffusely granular cortical surface affecting both kidneys symmetrically
B Multiple bilateral cortical cysts replacing normal parenchyma
C Smooth bilateral atrophy with a finely granular surface
D Coarse, irregular, asymmetric corticomedullary scars overlying blunted calyces

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Q6 PA27.11 1 pt

A 68-year-old man with a 30-year history of poorly controlled hypertension has progressive CKD. Renal biopsy shows concentric lamination of the arteriolar wall producing an 'onion-skin' appearance with luminal obliteration. This lesion is characteristic of:

A Malignant hypertension with hyperplastic arteriolosclerosis
B Benign nephrosclerosis with hyaline arteriolosclerosis
C Renal artery atherosclerosis causing renovascular hypertension
D Thrombotic microangiopathy with fibrin thrombi

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Q7 PA27.12 1 pt

A 7-year-old girl develops bloody diarrhoea after eating undercooked beef. Five days later she develops oliguria, haematuria, and thrombocytopenia. Her blood film shows fragmented red cells (schistocytes). ADAMTS13 levels are normal. The pathogenesis of her renal injury is best explained by:

A Autoimmune ADAMTS13 deficiency causing ultra-large vWF multimers
B Antineutrophil cytoplasmic antibody (ANCA)-mediated vasculitis
C Shiga toxin–mediated endothelial injury activating the complement and coagulation cascades
D Immune complex deposition causing membranoproliferative GN

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Q8 PA27.13 1 pt

A 45-year-old man is found to have bilateral flank masses on routine examination. Imaging reveals bilaterally enlarged kidneys with multiple cysts replacing the parenchyma. His father died of a subarachnoid haemorrhage at age 50. The gene most likely mutated in this patient encodes:

A PKD2 (polycystin-2) on chromosome 4
B VHL (von Hippel–Lindau) on chromosome 3p
C WT1 (Wilms tumour suppressor) on chromosome 11
D PKD1 (polycystin-1) on chromosome 16

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Q9 PA27.14 1 pt

A 55-year-old obese man presents with left flank pain. Plain X-ray of the abdomen shows a radiolucent filling defect in the left renal pelvis. Urinalysis reveals a pH of 5.0. Stone composition is most likely:

A Uric acid — radiolucent, associated with persistently acidic urine
B Calcium oxalate — radiopaque, envelope-shaped crystals
C Struvite (magnesium ammonium phosphate) — staghorn configuration
D Cystine — radiopaque due to sulphur content

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Q10 PA27.15 1 pt

A 70-year-old man with benign prostatic hyperplasia presents with bilateral hydronephrosis and rising creatinine. The primary mechanism of progressive renal damage in chronic hydronephrosis is:

A Ascending bacterial infection leading to chronic pyelonephritis
B Increased intratubular pressure causing tubular atrophy and interstitial fibrosis
C Immune complex–mediated glomerular injury from urinary stasis
D Direct pressure necrosis of the renal papillae by the calculus

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Q11 PA27.17 1 pt

A 60-year-old smoker presents with painless gross haematuria. Cystoscopy reveals a papillary lesion in the bladder trigone. Urinary cytology shows atypical cells. The most important occupational carcinogen associated with this malignancy is:

A Asbestos fibres
B Vinyl chloride monomer
C Aromatic amines (β-naphthylamine, benzidine)
D Radon gas

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Q12 PA27.16 1 pt

CLINICAL VIGNETTE: A 62-year-old man presents with a 2-month history of left flank pain, visible haematuria, and a palpable left abdominal mass. CT scan shows a 9 cm heterogeneous left renal mass with involvement of the left renal vein and a pulmonary nodule ('cannonball metastasis'). Serum calcium is 12.5 mg/dL. The tumour most likely arises from and is driven by:

A Collecting duct epithelium; driven by chromosome 1p deletion
B Urothelial cells of the renal pelvis; driven by aromatic amine exposure
C Metanephric mesenchyme; driven by WT1 deletion on chromosome 11p
D Proximal tubular epithelium; driven by VHL tumour suppressor loss on 3p25

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Q13 PA27.16 1 pt

CLINICAL VIGNETTE: A 3-year-old girl presents with a large abdominal mass discovered incidentally by her mother during bathing. Ultrasound shows a well-encapsulated right renal mass. Histology reveals blastemal cells, stromal spindle cells, and poorly formed glomeruloid tubular structures. This triphasic pattern is diagnostic of:

A Clear cell renal cell carcinoma
B Wilms tumour (nephroblastoma)
C Renal angiomyolipoma (hamartoma)
D Mesoblastic nephroma

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Q14 PA27.11 1 pt

CLINICAL VIGNETTE: A 50-year-old woman with uncontrolled hypertension and microangiopathic haemolytic anaemia undergoes renal biopsy. Pathology shows fibrinoid necrosis of afferent arterioles with intraluminal fibrin-platelet thrombi in glomerular capillaries, alongside the onion-skin lesion in interlobular arteries. These findings together are most consistent with:

A Benign nephrosclerosis from long-standing mild hypertension
B Renal artery stenosis from fibromuscular dysplasia
C Malignant hypertension causing thrombotic microangiopathy (TMA)
D Chronic pyelonephritis with reflux nephropathy

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