NEET-PG 2013 - Internal Medicine Practice Questions

Q: In which condition is Cepacia syndrome most commonly associated?

Cystic fibrosis. ***Cystic fibrosis*** - **Cepacia syndrome** is a severe and often fatal complication in patients with **cystic fibrosis** caused by infection with bacteria of the *Burkholderia cepacia complex*. - Patients with cystic fibrosis have impaired mucociliary clearance, making them highly susceptible to chronic bacterial infections, including those leading to Cepacia syndrome. *Sarcoidosis* - **Sarcoidosis** is a multisystem inflammatory disease characterized by the formation of **non-caseating granulomas**, primarily affecting the lungs and lymph nodes. - It is not associated with bacterial infections causing Cepacia syndrome. *Tuberculosis* - **Tuberculosis** is caused by *Mycobacterium tuberculosis* and primarily affects the lungs, leading to granuloma formation and tissue destruction. - While it is a chronic bacterial infection, it does not typically lead to or interact with the *Burkholderia cepacia complex* in the way seen in Cepacia syndrome. *Immotile cilia syndrome* - Also known as **primary ciliary dyskinesia**, this condition involves defective ciliary function leading to recurrent respiratory infections and other issues like situs inversus. - Although patients have recurrent respiratory infections, **Cepacia syndrome** is not a characteristic or commonly associated complication.

Q: What is the most common cause of lobar consolidation?

Streptococcus. ***Streptococcus*** - **_Streptococcus pneumoniae_** is the **most common bacterial cause** of community-acquired pneumonia, frequently leading to lobar consolidation. [1] - It often presents with classic symptoms such as **sudden onset of fever**, productive cough with **rusty sputum**, and pleuritic chest pain. [1] *Mycoplasma* - **_Mycoplasma pneumoniae_** typically causes **"walking pneumonia"**, characterized by a more indolent course and often presents with **interstitial infiltrates** rather than dense lobar consolidation. - Though common, it is a less frequent cause of true lobar consolidation compared to _Streptococcus pneumoniae_. *Chlamydia* - **_Chlamydia pneumoniae_** causes atypical pneumonia, similar to _Mycoplasma_, presenting with less severe symptoms and **patchy infiltrates** or **interstitial patterns** rather than lobar consolidation. - It is a common cause of **atypical pneumonia** but not the leading cause of lobar consolidation. *Legionella* - **_Legionella pneumophila_** can cause severe pneumonia with consolidation, but it is **less common overall** than pneumococcal pneumonia. [1] - **Legionnaires' disease** is often associated with exposure to contaminated water sources and may present with **gastrointestinal and neurological symptoms** in addition to respiratory manifestations.

Q: Which of the following is not a clinical feature of Bronchiectasis?

Night sweats. ***Night sweats*** - While **night sweats** can be present in chronic infections, they are not considered a primary or defining clinical feature directly associated with the pathology of bronchiectasis itself. - They are more commonly linked with systemic conditions like **tuberculosis** or malignancy, which would require alternative diagnostic pathways. *Hemoptysis* - **Hemoptysis** (coughing up blood) is a common and often alarming symptom of bronchiectasis due to the inflammation and damage to the bronchial walls and underlying vasculature [1]. - Blood vessels in damaged airways are prone to rupture, leading to bleeding, which can range from blood-streaked sputum to massive hemorrhage [1]. *Chest pain* - **Chest pain** can occur in bronchiectasis, often related to the chronic cough, pleural inflammation, or musculoskeletal strain from persistent coughing. - It can also be a symptom if there's an associated infection or inflammation extending to the pleura. *Productive cough* - A **chronic productive cough** with significant amounts of purulent sputum is the hallmark symptom of bronchiectasis [1]. - This is due to the impaired mucociliary clearance and chronic infection within the dilated, damaged airways .

Q: The physiological marker of the last stage of acute asthma is

Increased carbon dioxide levels (Hypercapnia). ***Increased carbon dioxide levels (Hypercapnia)*** - In severe, acute asthma, **air trapping** and **muscle fatigue** lead to inadequate ventilation and impaired gas exchange [1]. - This results in a buildup of carbon dioxide in the blood, indicating impending **respiratory failure** and a critical stage of the asthma exacerbation [3]. *Hypocapnia* - **Hypocapnia**, or low blood CO2, is common in the **early stages** of an asthma attack due to **tachypnea** (rapid breathing) in an effort to compensate [1]. - As the condition worsens, the ability to ventilate adequately diminishes, leading to CO2 retention [3]. *Hyperoxia* - **Hyperoxia** means abnormally high levels of oxygen in the blood, which is generally not a physiological marker of acute asthma. - Patients with acute asthma typically experience **hypoxemia** (low oxygen levels) due to ventilation-perfusion mismatch [1]. *Alkalosis* - **Respiratory alkalosis** (high pH due to low CO2) can occur in the early stages as patients **hyperventilate**. - However, in the late stages, as CO2 builds up (**hypercapnia**), the patient shifts towards **respiratory acidosis** (low pH), which is a sign of severe compromise [2], [3].

Q: Which of the following is a characteristic finding in distal RTA?

Hypercalciuria. ***Hypercalciuria*** - **Hypercalciuria** is a characteristic finding in distal RTA (Type 1), leading to increased calcium in the urine. - This occurs due to reduced **distal tubular reabsorption of calcium** and increased bone resorption from chronic acidosis. *Urine pH 5.5** [1]. - A urine pH < 5.5 would suggest a normal kidney response to systemic acidosis, ruling out distal RTA. *Hypokalemia* - While hypokalemia can occur in distal RTA, it is not always present and is not the most definitive characteristic finding. - **Hypokalemia** is more characteristic of Type 1 RTA due to increased potassium excretion in an attempt to excrete H+ ions. *Nephrolithiasis* - **Nephrolithiasis** (kidney stones) is a common complication of distal RTA due to hypercalciuria and alkaline urine [2]. - However, hypercalciuria is the *reason* for the increased risk of nephrolithiasis, making it a more fundamental characteristic finding.

Q: Which of the following is not a feature of distal renal tubular acidosis

Hyperkalemia. ***Hyperkalemia*** - **Distal renal tubular acidosis (dRTA)** is characterized by impaired acid excretion, leading to metabolic acidosis. The impaired excretion of acid is often accompanied by impaired potassium secretion, resulting in **hypokalemia**, not hyperkalemia. - While hyperkalemia is a feature of **type 4 RTA**, which is characterized by hypoaldosteronism or renal tubular unresponsiveness to aldosterone, it is not a feature of **distal RTA (type 1)**. [1] *Normal anion gap* - **Distal RTA** is a form of **normal anion gap metabolic acidosis**, also known as **hyperchloremic metabolic acidosis**. [1] - The anion gap is calculated as [Na+] - ([Cl-] + [HCO3-]), and in dRTA, the bicarbonate loss is compensated by an increase in chloride, maintaining a normal anion gap. *Renal hypercalciuria* - **Distal RTA** is associated with **impaired acid excretion**, which leads to chronic metabolic acidosis. - This **acidosis** promotes the dissolution of bone, releasing calcium, and decreases tubular reabsorption of calcium, resulting in **hypercalciuria**. *Alkaline urine* - In **distal RTA**, the distal tubule is unable to acidify the urine due to a defect in hydrogen ion secretion. - This leads to a persistent **urine pH > 5.5** (typically alkaline or inappropriately normal) despite systemic acidosis, making it a key diagnostic feature. [1]

Q: Hyperkalemia aciduria is seen in

Type IV Renal Tubular Acidosis. Type IV Renal Tubular Acidosis - This condition is characterized by **hyperkalemia** and **aciduria**, often due to a deficiency in aldosterone or a renal tubular insensitivity to aldosterone [1]. - The impaired aldosterone action leads to reduced potassium excretion and decreased ammonium production, both contributing to **hyperkalemia** and metabolic acidosis [1]. *Type I Renal Tubular Acidosis* - Type I RTA (distal RTA) is characterized by a defect in acid secretion in the distal tubule, leading to **hypokalemia** and metabolic acidosis with persistently high urine pH [2]. - Patients typically excrete an alkaline urine despite systemic acidosis, contrasting with the aciduria seen with hyperkalemia [2]. *Sigmoidocolostomy procedure* - A sigmoidocolostomy can lead to **hyperchloremic metabolic acidosis** due to the reabsorption of chloride and excretion of bicarbonate by the colonic mucosa. - However, it typically causes **hypokalemia** as potassium is secreted into the colonic lumen from the blood. *Type II Renal Tubular Acidosis* - Type II RTA (proximal RTA) involves a defect in bicarbonate reabsorption in the proximal tubule, resulting in **hypokalemia** and metabolic acidosis. - The kidney's ability to acidify urine is still largely intact in the distal nephron once the bicarbonate buffer system is overwhelmed.

Q: A diabetic patient presents with hyperkalemia and urinary pH < 5.5. What is the MOST likely underlying cause?

Type IV RTA. ***Type IV RTA*** - Patients with **diabetes mellitus** frequently develop **hyporeninemic hypoaldosteronism**, leading to Type IV RTA [1]. - This condition is characterized by **hyperkalemia** and **acidosis** with a paradoxically low urinary pH (typically < 5.5). *Uremia* - **Uremia** can cause hyperkalemia and acidosis, but it is a broader term for severe kidney failure and not the most specific underlying cause for the given urinary findings. - While patients with uremia can have aciduria, the combination of **diabetic hyperkalemia** and acid urine points more directly to a specific tubular defect. *Primary hyperaldosteronism* - **Primary hyperaldosteronism** is characterized by **hypertension**, **hypokalemia**, and metabolic alkalosis, which is the opposite of the patient's presentation [1]. - This condition involves excessive aldosterone production, leading to increased potassium excretion [1]. *Type I Renal tubular acidosis* - **Type I RTA** (distal RTA) is characterized by the inability to acidify urine, resulting in a **urinary pH > 5.5** despite systemic acidosis [1]. - While it can cause hypokalemia (due to increased distal K+ secretion) and acidosis, the elevated urinary pH is a key differentiating factor from this patient's presentation [1].

Q: Calciphylaxis is a severe life-threatening condition. Which of the following is most commonly associated with it?

End stage Renal disease. ***End stage Renal disease*** - Calciphylaxis frequently occurs in patients with **end-stage renal disease**, primarily associated with **secondary hyperparathyroidism** [1] and **calcium-phosphate imbalance**. - It leads to **cutaneous ischemia** and necrosis, often requiring aggressive management due to its high **mortality rate**. *Parathyroidectomy* - While parathyroidectomy may affect calcium levels, it is not directly linked to calciphylaxis. - Calciphylaxis more commonly develops due to underlying **chronic renal failure** [1] rather than surgical interventions. *Hyperthyroidism* - Hyperthyroidism primarily causes symptoms related to metabolism, **thyroid hormone excess**, and does not lead to calciphylaxis. - There is no direct correlation between hyperthyroid states and the pathophysiology of calciphylaxis. *Medullary carcinoma thyroid* - This condition involves **medullary thyroid carcinoma**, associated with calcitonin production and does not cause calciphylaxis. - Patients typically experience **thyroid-related symptoms** rather than the vascular complications seen in calciphylaxis.

Q: What is the primary clinical feature of Henoch-Schonlein purpura?

Skin rash characterized by palpable purpura. ***Skin rash characterized by palpable purpura*** - **Palpable purpura** is the hallmark cutaneous manifestation of **Henoch-Schonlein purpura (HSP)**, a small-vessel vasculitis [1]. - This rash typically appears on the **lower extremities and buttocks**, reflecting the deposition of IgA in vessel walls [1]. *Abdominal pain due to vasculitis* - While **abdominal pain** is a common feature of HSP due to gastrointestinal vasculitis, it is not considered the primary clinical feature [1]. - Gastrointestinal involvement can manifest with pain, bleeding, and intussusception, but the **skin rash** is more consistently present and diagnostic. *Joint pain associated with the condition* - **Arthralgia** or **arthritis** (joint pain) is seen in a significant number of HSP patients, particularly in the knees and ankles. - However, it is a secondary manifestation, and not the **defining primary sign** of the disease. *Kidney involvement in the disease* - **Renal involvement**, presenting as hematuria and proteinuria, occurs in about one-third of HSP cases and can lead to serious long-term complications. - Despite its significance for prognosis, **kidney disease** is a later and not universally present feature, making the rash the most critical initial diagnostic clue.

Question 1

In which condition is Cepacia syndrome most commonly associated?

Accepted Answer

Cystic fibrosis

Answer

Immotile cilia syndrome

Answer

Sarcoidosis

Answer

Tuberculosis

Question 2

What is the most common cause of lobar consolidation?

Accepted Answer

Streptococcus

Answer

Mycoplasma

Answer

Chlamydia

Answer

Legionella

Question 3

Which of the following is not a clinical feature of Bronchiectasis?

Accepted Answer

Night sweats

Answer

Hemoptysis

Answer

Chest pain

Answer

Productive cough

Question 4

The physiological marker of the last stage of acute asthma is

Accepted Answer

Increased carbon dioxide levels (Hypercapnia)

Answer

Hypocapnia

Answer

Hyperoxia

Answer

Alkalosis

Question 5

Which of the following is a characteristic finding in distal RTA?

Accepted Answer

Hypercalciuria

Answer

Urine pH < 5.5

Answer

Hypokalemia

Answer

Nephrolithiasis

Question 6

Which of the following is not a feature of distal renal tubular acidosis

Accepted Answer

Hyperkalemia

Answer

Renal hypercalciuria

Answer

Normal anion gap

Answer

Alkaline urine

Question 7

Hyperkalemia aciduria is seen in

Accepted Answer

Type IV Renal Tubular Acidosis

Answer

Type I Renal Tubular Acidosis

Answer

Sigmoidocolostomy procedure

Answer

Type II Renal Tubular Acidosis

Question 8

A diabetic patient presents with hyperkalemia and urinary pH < 5.5. What is the MOST likely underlying cause?

Accepted Answer

Type IV RTA

Answer

Uremia

Answer

Primary hyperaldosteronism

Answer

Type I Renal tubular acidosis

Question 9

Calciphylaxis is a severe life-threatening condition. Which of the following is most commonly associated with it?

Accepted Answer

End stage Renal disease

Answer

Parathyroidectomy

Answer

Medullary carcinoma thyroid

Answer

Hyperthyroidism

Question 10

What is the primary clinical feature of Henoch-Schonlein purpura?

Accepted Answer

Skin rash characterized by palpable purpura

Answer

Abdominal pain due to vasculitis

Answer

Joint pain associated with the condition

Answer

Kidney involvement in the disease

NEET-PG 2013 — Internal Medicine