AIM β’ KMU EXAM PRACTICE
KMU Past Paper Practice
Topic 6 β Cystic and Congenital Renal Disorders: Polycystic Kidney Disease, PUJ Obstruction and Urinary Tract Anomalies
4th Year MBBS β’ 20 A-type Single Best Answer MCQs β’ Integrated Pathology, Medicine, Urology and Obstetrics & Gynaecology
Curriculum scope follows the supplied Topic 6 brief. :contentReference[oaicite:0]{index=0}
MCQ 1
Question:
A 62-year-old woman undergoes ultrasonography for nonspecific abdominal discomfort. A single, thin-walled renal cyst with clear fluid and no solid component is found. Renal function is normal and there is no family history of renal disease. Which classification best fits this lesion?
Options:
Autosomal dominant cystic disease
Developmental cystic dysplasia
Simple renal cyst
Autosomal recessive cystic disease
Acquired cystic kidney disease
Correct Answer: Simple renal cyst
Explanation: An isolated thin-walled cyst in an older adult with preserved renal function and no inherited pattern is most consistent with a simple renal cyst.
MCQ 2
Question:
A 58-year-old man with longstanding advanced renal failure has been receiving dialysis. Imaging now demonstrates numerous bilateral renal cysts. His kidneys had previously become small and there is no family history of cystic renal disease. Which disorder best explains the new imaging finding?
Options:
Autosomal dominant polycystic kidney disease
Autosomal recessive polycystic kidney disease
Multicystic dysplastic kidney
Medullary sponge kidney
Acquired cystic kidney disease
Correct Answer: Acquired cystic kidney disease
Explanation: Multiple cysts developing in the setting of longstanding advanced renal failure without an inherited pattern indicate acquired cystic kidney disease.
MCQ 3
Question:
A 49-year-old woman with ADPKD undergoes abdominal imaging because of increasing abdominal fullness. In addition to enlarged cystic kidneys, multiple cysts are seen in the liver while liver function remains preserved. Which interpretation is most appropriate?
Options:
The hepatic cysts are a recognized extrarenal manifestation of ADPKD
The hepatic cysts indicate conversion to ARPKD
The hepatic cysts confirm congenital hepatic fibrosis
The hepatic cysts indicate metastatic renal disease
The hepatic cysts are caused by PUJ obstruction
Correct Answer: The hepatic cysts are a recognized extrarenal manifestation of ADPKD
Explanation: ADPKD is a systemic cystic disorder; hepatic cysts are a well-recognized extrarenal manifestation and do not imply hepatic failure.
MCQ 4
Question:
A young adult whose father has ADPKD is being assessed as a potential living kidney donor. Ultrasonography is equivocal, but establishing whether the patient carries the familial disorder is important before donation. Which additional investigation is most appropriate?
Options:
Renal biopsy
Urine cytology
Voiding cystourethrography
Targeted genetic testing
Diuretic renography
Correct Answer: Targeted genetic testing
Explanation: Genetic testing is useful when imaging is equivocal and establishing a definite diagnosis has major implications, such as evaluation of a potential kidney donor.
MCQ 5
Question:
A 44-year-old man with established ADPKD develops recurrent episodes of severe colicky loin pain. Imaging identifies a ureteric calculus. Which feature of ADPKD most plausibly contributes to this complication?
Options:
Congenital absence of the collecting system
Abnormal urinary drainage with stone-promoting factors
Diffuse destruction of the ureteric epithelium
Failure of the kidneys to rotate normally
Persistent obstruction of the posterior urethra
Correct Answer: Abnormal urinary drainage with stone-promoting factors
Explanation: Distortion of renal architecture and urinary drainage, together with metabolic factors, increases the risk of nephrolithiasis in ADPKD.
MCQ 6
Question:
A 21-year-old man has intermittent left loin pain that becomes particularly severe after drinking a large volume of fluid. Ultrasound shows marked renal pelvic dilatation with a nondilated ureter. Which mechanism best explains the worsening pain after increased fluid intake?
Options:
Increased bladder pressure produces ureteric reflux
Renal cysts rupture as urine output rises
Higher urine flow produces urethral spasm
Increased filtration directly inflames the renal pelvis
Rapid pelvic distension occurs behind a fixed outflow obstruction
Correct Answer: Rapid pelvic distension occurs behind a fixed outflow obstruction
Explanation: Increased urine production rapidly distends the obstructed renal pelvis in PUJ obstruction, producing intermittent flank pain despite a nondilated distal ureter.
MCQ 7
Question:
A young adult with intermittent flank pain has imaging evidence of PUJ obstruction. Cross-sectional imaging shows a lower-pole renal vessel crossing the junction and compressing the urinary outflow tract. How should this cause be classified?
Options:
Acquired intraluminal obstruction
Inflammatory ureteric obstruction
Congenital extrinsic anatomical obstruction
Functional bladder outlet obstruction
Developmental urethral obstruction
Correct Answer: Congenital extrinsic anatomical obstruction
Explanation: A crossing lower-pole vessel can externally compress the PUJ and represents an anatomical extrinsic factor contributing to congenital PUJ obstruction.
MCQ 8
Question:
A 46-year-old man develops progressive hydronephrosis several months after treatment for an impacted stone near the pelviureteric junction. Imaging shows a short narrowed segment at the previous site of instrumentation. Which mechanism is most likely?
Options:
Acquired scar-related narrowing
Autosomal dominant cyst formation
Failure of renal ascent
Posterior urethral valve formation
Lower-pole fusion of the kidneys
Correct Answer: Acquired scar-related narrowing
Explanation: Previous stones or instrumentation can produce fibrosis and secondary narrowing at the PUJ, creating an acquired rather than congenital obstruction.
MCQ 9
Question:
A patient with suspected PUJ obstruction has hydronephrosis on ultrasound and recurrent renal colic. The urologist wants an investigation that can better define the urinary tract anatomy and simultaneously identify a possible calculus. Which study is most useful?
Options:
Urine cytology
Micturating cystourethrogram
Renal biopsy
CT urography
Serum creatinine measurement
Correct Answer: CT urography
Explanation: CT urography provides detailed anatomical information and can detect calculi or other structural causes contributing to upper urinary tract obstruction.
MCQ 10
Question:
A 29-year-old man is found to have a horseshoe kidney during investigation of recurrent urinary infections and renal stones. Renal function is preserved. Which feature of this anomaly best explains these complications?
Options:
Absence of functioning renal tubules
Abnormal position and drainage causing urinary stasis
Failure of the posterior urethra to canalize
Diffuse renal cyst formation after birth
Increased glomerular filtration from renal fusion
Correct Answer: Abnormal position and drainage causing urinary stasis
Explanation: Horseshoe kidneys have altered position and drainage, predisposing to urinary stasis, PUJ obstruction, infection and stone formation.
MCQ 11
Question:
A woman with a pelvic ectopic kidney has recurrent urinary infections despite normal overall renal function. Which anatomical consequence of renal ectopia most plausibly predisposes her to infection?
Options:
Loss of all renal concentrating ability
Abnormal ureteric course with impaired urinary drainage
Autosomal recessive inheritance of the ectopic kidney
Obstruction by posterior urethral valves
Bilateral absence of the collecting system
Correct Answer: Abnormal ureteric course with impaired urinary drainage
Explanation: An ectopic kidney can have an abnormal ureteric course and drainage pattern, promoting urinary stasis and recurrent infection despite preserved filtration.
MCQ 12
Question:
Imaging in a child shows two ureters arising from one kidney. The two channels join together before entering the urinary bladder through a single terminal ureter. Which description best fits this anomaly?
Options:
Renal malrotation
Complete ureteric duplication
Pelvic renal ectopia
Incomplete collecting-system duplication
Posterior urethral duplication
Correct Answer: Incomplete collecting-system duplication
Explanation: In incomplete duplication, two ureteric channels arise proximally but unite before entering the bladder; complete duplication retains two separate distal insertions.
MCQ 13
Question:
A child develops a tender midline swelling between the umbilicus and bladder. Imaging shows a closed cystic cavity along the embryological urachal tract without communication with either the bladder or umbilicus. Which anomaly is most likely?
Options:
Bladder exstrophy
Posterior urethral valve
Patent urachus
Urethral atresia
Urachal cyst
Correct Answer: Urachal cyst
Explanation: Persistence of the central portion of the urachus with closure at both ends produces a urachal cyst along the bladder-to-umbilicus tract.
MCQ 14
Question:
A premature male infant with severe posterior urethral valves has bilateral hydronephrosis and cannot be adequately decompressed through the urethra. A temporary method of low-pressure bladder drainage is required before later definitive management. Which procedure is most appropriate?
Options:
Vesicostomy
Pyeloplasty
Endopyelotomy
Partial nephrectomy
Ureteric reimplantation
Correct Answer: Vesicostomy
Explanation: Vesicostomy can provide temporary low-pressure urinary diversion when adequate urethral decompression or immediate valve ablation is not feasible.
MCQ 15
Question:
A boy with suspected congenital bladder outlet obstruction undergoes voiding cystourethrography. The study shows a dilated posterior urethra, a thick-walled bladder and bilateral vesicoureteric reflux. Which physiological disturbance best explains these findings?
Options:
Reduced renal plasma flow from renal artery stenosis
Loss of bladder sensory innervation
High intravesical pressure from persistent outlet obstruction
Failure of renal ascent during embryogenesis
Excessive urine production from collecting ducts
Correct Answer: High intravesical pressure from persistent outlet obstruction
Explanation: Posterior urethral valves create a high-pressure bladder, causing muscular hypertrophy and transmitting pressure backward to the ureters and kidneys.
MCQ 16
Question:
A 12-week pregnant woman has no urinary symptoms, but a properly collected urine culture shows significant bacterial growth. She feels well and asks whether treatment can be postponed because she has no dysuria or fever. What is the most appropriate management principle?
Options:
Observe unless flank pain develops
Delay treatment until the third trimester
Treat only if microscopic hematuria appears
Treat with an appropriate pregnancy-safe antimicrobial
Refer directly for surgical urinary drainage
Correct Answer: Treat with an appropriate pregnancy-safe antimicrobial
Explanation: Asymptomatic bacteriuria in pregnancy warrants treatment because untreated bacteriuria can ascend and cause clinically important maternal and pregnancy complications.
MCQ 17
Question:
A 24-week pregnant woman reports dysuria, urinary frequency and suprapubic discomfort. She is afebrile, has no vomiting and has no costovertebral angle tenderness. Urinalysis supports a lower urinary infection. Which management approach is most appropriate?
Options:
Obtain urine culture and give an appropriate oral antimicrobial
Admit for immediate surgical decompression of both kidneys
Withhold treatment until fever or flank pain develops
Treat as pyelonephritis with prolonged intravenous therapy
Perform renal biopsy before starting treatment
Correct Answer: Obtain urine culture and give an appropriate oral antimicrobial
Explanation: The absence of systemic features supports acute cystitis rather than pyelonephritis; pregnancy requires microbiological assessment and appropriate antimicrobial treatment.
MCQ 18
Question:
A 28-week pregnant woman presents with fever, vomiting, flank pain and marked costovertebral angle tenderness. A colleague suggests oral nitrofurantoin because it is commonly used for lower urinary infection. Why is this choice unsuitable for the current illness?
Options:
It causes immediate ureteric obstruction
It prevents urine culture from becoming positive
It increases renal cyst formation during pregnancy
It has no antibacterial activity in urine
It does not achieve adequate renal tissue levels for pyelonephritis
Correct Answer: It does not achieve adequate renal tissue levels for pyelonephritis
Explanation: Nitrofurantoin concentrates in urine and is useful for lower UTI, but inadequate renal parenchymal penetration makes it unsuitable for acute pyelonephritis.
MCQ 19
Question:
A 30-week pregnant woman is admitted with acute pyelonephritis. During observation she develops regular painful uterine contractions. Which pregnancy complication is most directly associated with this infection?
Options:
Fetal renal fusion
Preterm labor
Posterior urethral valve formation
Autosomal dominant renal cyst formation
Maternal renal agenesis
Correct Answer: Preterm labor
Explanation: Acute pyelonephritis during pregnancy can provoke uterine activity and is associated with important pregnancy complications including preterm labor.
MCQ 20
Question:
A 27-week pregnant woman with pyelonephritis is febrile, vomiting and tachycardic, with low blood pressure and marked flank tenderness. She cannot tolerate oral fluids. Which management principle is most appropriate?
Options:
Observe at home until the urine culture is repeated
Use symptomatic treatment without antimicrobials
Provide hospital care with parenteral antimicrobials and supportive therapy
Perform immediate bilateral pyeloplasty
Delay treatment until uterine contractions develop
Correct Answer: Provide hospital care with parenteral antimicrobials and supportive therapy
Explanation: Systemically ill pregnant patients with acute pyelonephritis require prompt hospital management, parenteral antimicrobial therapy, hydration and close maternal-fetal monitoring.