Nephrology — MCQs
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Which of the following is most commonly affected in Ormond's disease?
Which of the following biomarkers is not typically involved in the diagnosis of acute kidney injury?
What is the most common renal manifestation associated with leprosy?
Among the following, which is the most characteristic urinary finding in chronic renal failure (CRF)?
Most common cause of hypernatremia.
Chronic hemodialysis in ESRD patient is done
A 48-year-old man presents with complaints of facial puffiness, frothy urine, and hypertension. He gives a history of infection with hepatitis B. Urine examination reveals microscopic hematuria. The histopathological image of the kidney biopsy shows a spike and dome pattern. What is the diagnosis of this condition?
A 40-year-old man with a known case of hypertension presented with multiple episodes of hematuria and loin pain. His elder brother passed away due to a stroke at the age of 40. What is the probable diagnosis based on the clinical presentation?
What is the most likely cause of metabolic acidosis in a patient with a pH of 7.2, HCO3- levels of 10 or 12, and pCO2 of 35 mmHg?
A 51-year-old person came with a complaint of hematuria. On examination, he was normotensive and had pedal edema. Investigations revealed the patient had no glucosuria and had a creatinine value of 9mg%. Renal biopsy is as shown below. Which of the following investigations should be done to identify the etiology of the disease?
Nephrology Indian Medical PG Practice Questions and MCQs
Question 771: Which of the following is most commonly affected in Ormond's disease?
- A. Aorta
- B. IVC
- C. Ureter (Correct Answer)
- D. Gonadal vessels
Explanation: Ureter - Ormond's disease, also known as **retroperitoneal fibrosis (RPF)**, is characterized by the development of a dense fibrous tissue mass in the retroperitoneum, most commonly encasing and compressing the **ureters**. - This compression can lead to **ureteral obstruction** and subsequent **hydronephrosis**. Aorta - While the aorta can be involved in retroperitoneal fibrosis, it is typically encased rather than directly affected in a way that causes primary aortic disease. - The **fibrotic process** can adhere to and surround the great vessels, but the ureters are more prone to symptomatic compression. IVC - The **inferior vena cava (IVC)** can also be compressed or encased by the fibrotic tissue in Ormond's disease. - However, **ureteral involvement** leading to obstruction is a more common and clinically significant presentation than primary IVC compression. Gonadal vessels - Although **gonadal vessels** course through the retroperitoneum, they are less commonly the primary structures affected or severely compromised by the fibrotic process compared to the ureters. - Their involvement is usually secondary to widespread retroperitoneal fibrosis rather than being the most commonly affected site.
Question 772: Which of the following biomarkers is not typically involved in the diagnosis of acute kidney injury?
- A. Cystatin C
- B. NGAL
- C. KIM 1
- D. Micro RNA 122 (Correct Answer)
Explanation: Micro RNA 122 - **MicroRNA-122** is primarily a biomarker for **liver injury** [1] and not typically used in the diagnosis of **acute kidney injury (AKI)**. - Its expression is highly enriched in the liver and is released into circulation upon **hepatocyte damage**. *NGAL* - **Neutrophil gelatinase-associated lipocalin (NGAL)** is an early biomarker for **AKI**, found in both urine and plasma. - It rapidly increases in response to **renal tubular damage**, making it useful for early detection. *KIM 1* - **Kidney injury molecule-1 (KIM-1)** is a transmembrane protein expressed at very low levels in healthy kidneys but significantly upregulated in the **proximal tubular epithelial cells** during **AKI** [2]. - Its presence in urine is a strong indicator of **renal tubular injury**. *Cystatin C* - **Cystatin C** is a **glomerular filtration rate (GFR)** marker that increases in the blood earlier than creatinine in cases of **AKI**. - It is unaffected by muscle mass, age, or sex, making it a more reliable indicator of **renal function decline** in certain populations.
Question 773: What is the most common renal manifestation associated with leprosy?
- A. Acute glomerulonephritis
- B. Membranoproliferative glomerulonephritis
- C. Membranous glomerulonephritis (Correct Answer)
- D. Mesangioproliferative glomerulonephritis
Explanation: ***Membranous glomerulonephritis*** - **Membranous glomerulonephritis** is the most frequently reported renal lesion in leprosy, often associated with a **lepromatous form** of the disease. [2] - This is due to the deposition of **immune complexes** containing *Mycobacterium leprae* antigens in the glomerular basement membrane. [2] *Acute glomerulonephritis* - While possible in some infections, **acute glomerulonephritis** is not specifically or most commonly linked to leprosy. - It’s often characterized by **abrupt onset** of hematuria, proteinuria, and renal dysfunction. [1] *Membranoproliferative glomerulonephritis* - **Membranoproliferative glomerulonephritis** is a less common renal manifestation in leprosy. - It results from immune complex deposition causing mesangial and endothelial cell proliferation, often associated with other chronic infections but less so with leprosy specifically. [3] *Mesangioproliferative glomerulonephritis* - **Mesangioproliferative glomerulonephritis** involves proliferation of mesangial cells and can be seen in various conditions. - However, it is not the dominant or most common renal finding in patients with leprosy, which primarily involves subepithelial immune complex deposition.
Question 774: Among the following, which is the most characteristic urinary finding in chronic renal failure (CRF)?
- A. Elevated blood urea
- B. Bleeding diathesis
- C. Broad casts in urine (Correct Answer)
- D. Proteinuria
Explanation: ***Broad casts in urine*** [3] - **Broad casts** are pathognomonic for **chronic renal failure (CRF)** and signify irreversible nephron loss because they are formed in dilated tubules that have undergone compensatory hypertrophy. - They are composed of cellular debris and Tamm-Horsfall protein and indicate severe and long-standing renal parenchymal damage. *Elevated blood urea* - While elevated blood urea, or **azotemia**, is characteristic of CRF, it is a blood chemistry finding, not a urinary finding [3], [4]. - It reflects impaired glomerular filtration and accumulation of nitrogenous waste products. *Bleeding diathesis* - **Bleeding diathesis** is a common complication of CRF due to uremia-induced platelet dysfunction, but it is a systemic clinical manifestation, not a urinary finding [1]. - It manifests as easy bruising, epistaxis, or prolonged bleeding. *Proteinuria* - **Proteinuria** is a common finding in many forms of kidney disease, including CRF, but it is not the most *characteristic* finding specifically for the **chronicity** and severity of CRF [2]. - Its presence indicates glomerular or tubular injury, but broad casts offer more specific evidence of advanced, irreversible damage.
Question 775: Most common cause of hypernatremia.
- A. Carcinoid syndrome
- B. Adipsic diabetes insipidus
- C. Sweating
- D. Renal losses (Correct Answer)
Explanation: ***Renal losses*** - **Renal losses** are a very common cause of hypernatremia, particularly when the kidneys cannot adequately reabsorb water, leading to increased free water excretion. [1] - This can be seen in conditions like **diabetes insipidus (central or nephrogenic)**, where there is either a deficiency of ADH or renal unresponsiveness to ADH, resulting in dilute urine and high serum sodium. [1] *Adipsic diabetes insipidus* - **Adipsic diabetes insipidus** is a rare form of central diabetes insipidus characterized by impaired thirst sensation. [2] - While it directly leads to profound hypernatremia, its **rarity** makes it an uncommon overall cause compared to other etiologies. *Carcinoid syndrome* - **Carcinoid syndrome** is caused by tumors that release excessive amounts of vasoactive substances, like serotonin. - It is primarily associated with symptoms like flushing, diarrhea, and bronchospasm, and **does not directly cause hypernatremia**. *Sweating* - **Sweating** causes loss of hypotonic fluid (more water than electrolytes), which can lead to hypernatremia if not adequately replaced. - While a contributing factor, severe hypernatremia specifically due to sweating alone is **less common** than that caused by renal free water losses, especially in the context of impaired thirst or access to water.
Question 776: Chronic hemodialysis in ESRD patient is done
- A. Once per week
- B. Twice per week
- C. Thrice per week (Correct Answer)
- D. Daily
Explanation: ***Thrice per week*** - **Standard chronic hemodialysis** for **end-stage renal disease (ESRD)** patients is typically performed **three times per week** to adequately remove waste products and excess fluid. - This frequency is established to maintain a balance between effective treatment and the patient's quality of life, allowing for sufficient recovery time between sessions. *Once per week* - This frequency is generally **insufficient** for adequate solute and fluid removal in most ESRD patients, leading to **uremic symptoms** and complications. - Would likely result in **poor patient outcomes** due to accumulation of toxins and fluid overload. *Twice per week* - While sometimes considered for patients with **significant residual renal function** or those transitioning to another modality, it is **often inadequate** for long-term maintenance in most ESRD patients. - May lead to **suboptimal dialysis adequacy** and requires close monitoring for signs of under-dialysis. *Daily* - **Daily hemodialysis** (short daily or nocturnal daily) is an optimized regimen that can offer **better clearance** and **blood pressure control** [1] but is **not the standard chronic regimen**. - It imposes a **higher burden** on the patient's time and resources, and is typically reserved for specific clinical situations where standard thrice-weekly treatment is insufficient.
Question 777: A 48-year-old man presents with complaints of facial puffiness, frothy urine, and hypertension. He gives a history of infection with hepatitis B. Urine examination reveals microscopic hematuria. The histopathological image of the kidney biopsy shows a spike and dome pattern. What is the diagnosis of this condition?
- A. Minimal change disease
- B. Membranous nephropathy (Correct Answer)
- C. FSGS
- D. Post-streptococcal glomerulonephritis (PSGN)
Explanation: ***Membranous nephropathy*** - The **spike and dome pattern** seen in the biopsy is characteristic of membranous nephropathy [1,5], which also explains the patient's **facial puffiness** and frothy urine due to nephrotic syndrome [2,4]. - The association with **hepatitis B** infection further supports this diagnosis, as HBV can lead to a secondary form of membranous nephropathy [4]. *Minimal change disease* - Typically presents with **edema** and **proteinuria**, but does not show a spike and dome pattern on biopsy [3]. - It is often associated with **children** and responds well to steroids, unlike the findings here [3]. *FSGS* - Presents with **nephrotic syndrome** and may show varying degrees of scarring on biopsy, but lacks the characteristic spike and dome appearance [3,5]. - FSGS can also be secondary to other conditions but is not typically linked with hepatitis B. *PSGN-associated disease* - Post-streptococcal glomerulonephritis (PSGN) usually results in **hematuria** and **hypertension** following a streptococcal infection, not hepatitis B [2]. - The histopathological findings would more likely show **proliferative changes** rather than a spike and dome pattern [2]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, p. 921. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, p. 915. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, pp. 927-928. [4] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, pp. 919-921. [5] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Diseases Of The Urinary And Male Genital Tracts, pp. 531-532.
Question 778: A 40-year-old man with a known case of hypertension presented with multiple episodes of hematuria and loin pain. His elder brother passed away due to a stroke at the age of 40. What is the probable diagnosis based on the clinical presentation?
- A. Renal cell carcinoma
- B. Tuberculosis of the kidney
- C. Autosomal recessive polycystic kidney disease
- D. Autosomal dominant polycystic kidney disease (Correct Answer)
Explanation: ***Autosomal dominant polycystic kidney disease*** - The patient's presentation with **pain**, **hematuria**, and **hypertension** is typical for **ADPKD**. The family history of a brother dying of a **stroke** at a young age suggests a genetic predisposition to vascular abnormalities, common in ADPKD. - **Cerebral aneurysms**, which can lead to stroke, are a known extranal manifestation of ADPKD, and early onset stroke in a sibling strengthens the diagnosis despite it not being the defining feature of ADPKD itself. *Renal cell carcinoma* - While **hematuria**, **loin pain**, and **hypertension** can be symptoms of renal cell carcinoma, the bilateral nature of the cysts seen in the image and the family history of **early stroke** make ADPKD a more probable diagnosis. - Renal cell carcinoma usually presents as a **unilateral** solid mass, not diffuse cystic changes in both kidneys. *Tuberculosis of the kidney* - Renal tuberculosis would present with symptoms like sterile pyuria, dysuria, and flank pain, but less commonly with the dramatic cystic changes and family history of stroke seen here. - The imaging would typically show cavitary lesions or hydronephrosis rather than widespread bilateral cysts. *Autosomal recessive polycystic kidney disease* - **ARPKD** typically presents in **infancy or childhood** with severe renal failure and liver involvement. - The patient's age (40 years) makes ARPKD highly unlikely, as individuals with this condition rarely survive into adulthood without significant medical intervention.
Question 779: What is the most likely cause of metabolic acidosis in a patient with a pH of 7.2, HCO3- levels of 10 or 12, and pCO2 of 35 mmHg?
- A. Increased potassium excretion by the kidneys
- B. Increased hydrogen ion excretion by the kidneys
- C. Loss of bicarbonate by the kidneys (Correct Answer)
- D. Increased carbon dioxide expiration by the lungs
Explanation: ***Loss of bicarbonate by the kidneys*** - A pH of 7.2 (acidosis) and low **HCO3- (10-12 mEq/L)**, with a near-normal **pCO2 (35 mmHg)**, indicates an uncompensated **metabolic acidosis** [1], [3]. - Renal tubular acidosis (RTA), particularly **Type 2 RTA**, is characterized by impaired bicarbonate reabsorption by the proximal renal tubules, leading to excessive loss of bicarbonate in the urine, resulting in metabolic acidosis [2]. *Increased potassium excretion by the kidneys* - While certain renal conditions can lead to **potassium wasting**, this directly contributes to **hypokalemia**, not primarily to the observed metabolic acidosis. - While some **RTAs (Type 1 and Type 2) are associated with hypokalemia**, the direct cause of acidosis is bicarbonate loss or impaired acid excretion [2]. *Increased hydrogen ion excretion by the kidneys* - **Increased hydrogen ion excretion** would typically help correct acidosis, not cause it. - This process is crucial for acid-base balance, and its effective functioning would lead to **alkalosis** or normalization of pH, not acidosis. *Increased carbon dioxide expiration by the lungs* - **Increased CO2 expiration** would lead to a decrease in **pCO2**, which is a **respiratory alkalosis** or a compensatory mechanism for metabolic acidosis, not the cause of the acidosis itself [1]. - The given pCO2 of 35 mmHg is within or near the normal range, indicating the lungs are either not compensating fully or not the primary cause of the acidosis.
Question 780: A 51-year-old person came with a complaint of hematuria. On examination, he was normotensive and had pedal edema. Investigations revealed the patient had no glucosuria and had a creatinine value of 9mg%. Renal biopsy is as shown below. Which of the following investigations should be done to identify the etiology of the disease?
- A. ANA
- B. ANTI GBM antibodies (Correct Answer)
- C. HIV RNA
- D. Urine immunoelectrophoresis
Explanation: ***ANTI GBM antibodies*** - The presence of hematuria and renal failure suggests a possible **glomerulonephritis**, where **anti-GBM (Glomerular Basement Membrane) antibodies** would help confirm conditions like Goodpasture syndrome [2]. - This test specifically identifies **anti-GBM disease** [1,2], which is crucial in guiding management for this patient with suspected renal pathology [3]. *ANA* - **Antinuclear antibody (ANA)** testing is typically used for autoimmune diseases like **Systemic Lupus Erythematosus** but is less specific for glomerular diseases. - In this context, ANA would not specifically help in identifying the **etiology of renal failure** associated with hematuria. *Urine immunoelectrophoresis* - This test is primarily useful for detecting **light chains** in conditions like **multiple myeloma** and may not be relevant to general hematuria or renal failure. - It is not a direct test for **glomerular disease etiology** related to hematuria and edema. *HIV RNA* - While **HIV** can lead to renal complications, including **HIV-associated nephropathy**, this test is not the first line for etiological determination in this specific presentation. - Negative **HIV serology** doesn't rule out renal disease caused by other factors, making this test less relevant here. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Diseases Of The Urinary And Male Genital Tracts, pp. 526-527. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Diseases Of The Urinary And Male Genital Tracts, pp. 537-538. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, pp. 918-919.
Practice by Chapter
Acute Kidney Injury
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Chronic Kidney Disease
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Glomerular Diseases
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Tubulointerstitial Diseases
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Nephrotic and Nephritic Syndromes
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Urinary Tract Infections
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Renal Replacement Therapy
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Fluid and Electrolyte Disorders
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Acid-Base Disorders
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Kidney in Systemic Diseases
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Kidney Stones and Obstructive Uropathy
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Hypertension in Kidney Disease
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