Anatomy
1 questionsPodocytes are seen in -
NEET-PG 2012 - Anatomy NEET-PG Practice Questions and MCQs
Question 341: Podocytes are seen in -
- A. Bowman's capsule (Correct Answer)
- B. Proximal convoluted tubule
- C. Distal convoluted tubule
- D. Collecting tubule of the kidney
Explanation: **Bowman's capsule** - **Podocytes** are specialized epithelial cells that form the **visceral layer** of Bowman's capsule. They have foot processes (pedicels) that interdigitate to form slit diaphragms, which are crucial for the **filtration barrier** of the glomerulus [1]. - These cells facilitate the selective passage of water and small solutes from the blood into Bowman's space, while preventing the filtration of large proteins and blood cells. *Proximal convoluted tubule* - The **proximal convoluted tubule** is primarily involved in the **reabsorption** of essential nutrients, ions, and water from the filtrate back into the bloodstream [1]. - Its cells are characterized by a **brush border** (microvilli) and numerous mitochondria, indicating high metabolic activity, and are not podocytes [1]. *Distal convoluted tubule* - The **distal convoluted tubule** plays a role in fine-tuning the reabsorption of ions and water, under the influence of hormones like **aldosterone** and **ADH**. - Its cells lack the specialized foot processes and filtration function characteristic of podocytes. *Collecting tubule of the kidney* - The **collecting tubule** (or collecting duct) is involved in regulating water reabsorption and acid-base balance, responding to **ADH** to concentrate urine. - Its epithelial cells are principal cells and intercalated cells, which are different in structure and function from podocytes.
Biochemistry
1 questionsWhat is the most sensitive biochemical marker for a 7-day old myocardial infarction?
NEET-PG 2012 - Biochemistry NEET-PG Practice Questions and MCQs
Question 341: What is the most sensitive biochemical marker for a 7-day old myocardial infarction?
- A. CPK MB
- B. LDH
- C. Myoglobin
- D. Troponin I/T (Correct Answer)
Explanation: ***Troponin I/T*** - **Cardiac troponins (I and T)** are highly sensitive and specific biomarkers for **myocardial injury**. - While they rise quickly after an MI, they also remain elevated for an extended period, typically **7 to 10-14 days**, making them ideal for detecting a 7-day-old event. *CPK MB* - **Creatine phosphokinase MB (CPK-MB)** is a well-known cardiac marker, but its elevation is more transient, usually returning to normal within **2-3 days** post-MI. - Therefore, it would likely be undetectable or near baseline 7 days after the event, making it insensitive for this duration. *LDH* - **Lactate dehydrogenase (LDH)** used to be used as a cardiac marker, but it is **non-specific** and found in various tissues. - While it can remain elevated for an extended period after an MI (up to 10-14 days), its lack of specificity makes other markers, particularly troponins, much more reliable for confirming myocardial damage. *Myoglobin* - **Myoglobin** is one of the earliest markers to rise after myocardial injury, but it is also **rapidly cleared** from the bloodstream, usually within 24 hours. - Due to its short half-life, myoglobin would not be elevated 7 days after an MI, making it unsuitable for detecting such a remote event.
Internal Medicine
4 questionsWhat is the term for the collapse of a lung?
Which condition is commonly associated with Disseminated Intravascular Coagulation (D.I.C.)?
All of the following provide protection against malaria except which of the following?
What is the frequency of renal involvement in Henoch-Schönlein purpura (HSP)?
NEET-PG 2012 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 341: What is the term for the collapse of a lung?
- A. Emphysema
- B. Atelectasis (Correct Answer)
- C. Bronchitis
- D. Bronchiectasis
Explanation: ***Atelectasis*** - **Atelectasis** is the technical term for the **collapse of a lung** or a part of a lung, leading to reduced or absent gas exchange. - It can be caused by **obstruction of the airway** (e.g., mucus plug, foreign body) or external compression on the lung [1]. *Emphysema* - **Emphysema** is a chronic lung disease characterized by the **destruction of the alveoli**, leading to permanent enlargement of airspaces [2]. - It results in reduced elastic recoil of the lungs and is a type of **COPD (chronic obstructive pulmonary disease)** [2]. *Bronchiectasis* - **Bronchiectasis** is a chronic condition where the airways (bronchi) become **abnormally widened** and scarred. - This widening leads to a buildup of mucus, making the lungs vulnerable to **recurrent infections**. *Bronchitis* - **Bronchitis** is an inflammation of the lining of the bronchial tubes, which carry air to and from your lungs. - It typically causes a **cough** with mucus production and can be acute or chronic.
Question 342: Which condition is commonly associated with Disseminated Intravascular Coagulation (D.I.C.)?
- A. Acute myelomonocytic leukemia
- B. Chronic myeloid leukemia
- C. Autoimmune hemolytic anemia
- D. Acute promyelocytic leukemia (Correct Answer)
Explanation: ***Acute promyelocytic leukemia*** - **Disseminated Intravascular Coagulation (D.I.C.)** is commonly associated with acute promyelocytic leukemia due to the release of **tissue factor** from promyelocytes [1]. - Patients typically present with **severe bleeding** and coagulopathy [1], driven by the rapid proliferation of these abnormal cells. *Acute myelomonocytic leukemia* - While this type of leukemia presents with myelomonocytic features, it is less frequently associated with **D.I.C.** compared to acute promyelocytic leukemia. - This condition is often characterized by **monocytic infiltration** but does not typically cause the severe coagulopathy associated with D.I.C. *Autoimmune hemolytic anemia* - This condition causes **hemolysis** due to antibodies but is mainly associated with **anemia**, not a coagulation disorder like D.I.C. - **D.I.C.** involves widespread **consumption coagulopathy** [1], which is not a feature of autoimmune hemolytic anemia. *CMC* - CMC refers to **Chronic Myeloid Leukemia**, which does not commonly lead to **D.I.C.** and presents primarily with splenomegaly and **chronic symptoms**. - The coagulation profile in CMC tends to be stable, with no link to the acute coagulopathy seen in D.I.C.
Question 343: All of the following provide protection against malaria except which of the following?
- A. PNH (Correct Answer)
- B. Sickle cell anemia
- C. Hereditary spherocytosis
- D. Duffy blood group
Explanation: ***PNH*** - Paroxysmal Nocturnal Hemoglobinuria (PNH) does not provide any **protection against malaria**; it is an acquired bone marrow disorder. - While it leads to increased hemolysis and thrombosis, it does not affect **malaria susceptibility** directly. *Duffy blood group* - The Duffy blood group has specific antigens that are a **receptor for Plasmodium vivax**, making individuals with a Duffy-negative phenotype resistant to this type of malaria. - Therefore, Duffy blood group status can indeed serve as a protective factor against certain malaria strains. *Hereditary spherocytosis* - This condition results in **spherical red blood cells** [1], causing hemolytic anemia, but it does not confer protection against malaria. - People with hereditary spherocytosis do not have a lower prevalence of malaria and may still be susceptible to infection. *Sickle cell anemia* - Individuals with sickle cell anemia often exhibit **increased resistance to malaria**, especially against Plasmodium falciparum [2]. - The sickling of red blood cells under low oxygen conditions creates an unfavorable environment for the malarial parasites to thrive [2, 3].
Question 344: What is the frequency of renal involvement in Henoch-Schönlein purpura (HSP)?
- A. 25-35%
- B. 60-80%
- C. 40-60% (Correct Answer)
- D. 5-10%
Explanation: ***40-60%*** - Renal involvement in Henoch-Schönlein purpura (HSP) is common, affecting approximately **40-60% of patients**. - Renal complications can range from microscopic hematuria to proteinuria, and in some cases, **progressive glomerulonephritis** leading to renal failure. *25-35%* - This percentage underestimates the actual frequency of **renal complications** in HSP. - While mild symptoms might fall within this range, a broader spectrum of renal manifestations is observed. *60-80%* - This percentage overestimates the reported frequency of **renal involvement** in HSP. - Although it is common, a majority of patients do not develop renal symptoms. *5-10%* - This range is too low for the frequency of **renal involvement** in HSP. - Even though it's benign in many cases, some form of renal pathology like hematuria is quite frequent.
Pathology
4 questionsWhich tumor marker is most commonly associated with lung and breast carcinoma?
Vegetations in Libman-Sacks endocarditis are:
Medial calcification is seen in -
What is the most common cause of nephritic syndrome in adults, excluding IgA nephropathy?
NEET-PG 2012 - Pathology NEET-PG Practice Questions and MCQs
Question 341: Which tumor marker is most commonly associated with lung and breast carcinoma?
- A. CEA (Correct Answer)
- B. hCG
- C. AFP
- D. CA-15-3
Explanation: ***CEA*** - **Carcinoembryonic antigen (CEA)** is a tumor marker commonly associated with **lung** and **breast cancers** [1]. - Elevated levels of CEA are often observed in **various malignancies**, making it useful for monitoring treatment response and recurrence. *CA-15-3* - While **CA-15-3** is a breast cancer marker, it is less specific than CEA and often used primarily for **monitoring** but not for initial diagnosis. - It is primarily elevated in **breast carcinoma**, not typically associated with **lung cancer**. *11CG* - This ppears to be incorrectly referenced and may not exist as a recognized tumor marker for lung or breast cancer. - There are no clinical associations with lung or breast cancer, making it irrelevant in this context. *AFP* - **Alpha-fetoprotein (AFP)** is primarily associated with **liver** and **germ cell tumors**, not commonly associated with lung or breast cancers [1]. - Elevated AFP levels do not correlate with lung or breast carcinomas, distinguishing it from CEA's relevance. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Neoplasia, p. 346.
Question 342: Vegetations in Libman-Sacks endocarditis are:
- A. Large and fragile
- B. Small warty along the line of closure of valve
- C. Small or medium sized on either or both sides of valve (Correct Answer)
- D. Small bland vegetations
Explanation: ***Small or medium sized on either or both sides of valve*** - **Libman-Sacks endocarditis** typically presents with vegetations that are **small to medium in size**, found on either aspect of the valve leaflets [1][2][3]. - These vegetations are **sterile**, non-infectious, and often associated with systemic lupus erythematosus (SLE) [2][3]. *Large and fragile* - Vegetations in Libman-Sacks endocarditis are not typically **large**; they are small or medium [1]. - The term **fragile** is misleading, as the vegetations are not characterized by fragility but by being sturdy yet non-infectious. *Small warty along the line of closure of valve* - While the vegetations are small, they are **not warty** and do not primarily form along the line of closure, which is common in infective endocarditis [1]. - Libman-Sacks vegetations can be found on either side of the valve, unlike warty vegetations [1]. *Small bland vegetations* - Vegetations in Libman-Sacks endocarditis are bland but not solely described as **small and bland**; their presence on either or both sides of the valve is critical [1]. - This option fails to capture the significance of their size and localization in the endocardial lesions associated with SLE. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Heart, p. 568. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of the Immune System, pp. 232-233. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Heart, p. 570.
Question 343: Medial calcification is seen in -
- A. Atherosclerosis
- B. Arteriolosclerosis
- C. Dissecting aneurysm
- D. Monckeberg's sclerosis (Correct Answer)
Explanation: ***Monckeberg's sclerosis*** - This condition is characterized by **calcific deposits** within the **tunica media** of muscular arteries. - It typically does not occlude the vessel lumen and is often asymptomatic, though severe calcification can lead to vessel rigidity. *Atherosclerosis* - Involves the formation of **atheromatous plaques** in the **tunica intima** of large and medium-sized arteries. - These plaques consist of lipids, inflammatory cells, smooth muscle cells, and fibrous connective tissue, leading to luminal narrowing and hardening of arteries. *Arteriolosclerosis* - Refers to the thickening and hardening of the walls of **arterioles** (small arteries). - It is often associated with hypertension and diabetes, affecting resistance vessels but typically not involving extensive medial calcification. *Dissecting aneurysm* - This condition involves a **tear in the tunica intima** of an artery, allowing blood to enter and dissect between the layers of the arterial wall. - It is a life-threatening condition primarily affecting the aorta and is characterized by a false lumen, not medial calcification.
Question 344: What is the most common cause of nephritic syndrome in adults, excluding IgA nephropathy?
- A. FSGS
- B. Membranous glomerulonephritis
- C. Membranoproliferative glomerulonephritis (Correct Answer)
- D. Post-infectious glomerulonephritis
Explanation: ***None*** - Nephritic syndrome in adults is often caused by various conditions, but there is **no single most common cause** that universally applies. - The true prevalence can vary by population, but conditions like **IgA nephropathy** or **post-infectious glomerulonephritis** [1] are frequently encountered rather than one specific disease. *Membranoproliferative glomerulonephritis* - This condition can cause a **nephritic syndrome** [1], but it is not the most common cause in adults, often seen in association with **hepatitis C** or other infections. - In practice, **IgA nephropathy** or **post-streptococcal glomerulonephritis** [1] are more frequently recognized causes of nephritic syndrome in adults. *Membranous glomerulonephritis* - Primarily presents with **nephrotic syndrome** rather than nephritic features [1], making it less likely to be cited as a common cause of nephritic syndrome. - It is associated with **anti-phospholipase A2 receptor antibodies** but lacks the inflammatory features of nephritis [1]. *FSGN* - **Focal Segmental Glomerulosclerosis** is associated with nephrotic syndrome and doesn't typically lead to classic nephritic features, such as hematuria and hypertension [1]. - Its primary presentation is with **proteinuria** and possible renal failure but not with the typical characteristics of nephritic syndrome [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, pp. 915-919.