In which condition is the Doll's Eye Reflex tested?
In which condition is Serum Amyloid Associated (SAA) protein most commonly found?
In evaluation of a case of immotile nasal cilia, which of the following investigations should prove useful?
Saddle nose deformity is seen in?
Which of the following statements regarding Pertussis is INCORRECT?
Post-tubercular bronchiectasis is most commonly seen with
Central bronchiectasis is seen with
Which of the following is seen in sarcoidosis
Aspirin sensitive asthma is associated with:
Which of the following is the common cause of respiratory failure type 2 ?
NEET-PG 2015 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 31: In which condition is the Doll's Eye Reflex tested?
- A. Hemiplegic
- B. Paraplegic
- C. Cerebral palsy
- D. Unconscious patients (Correct Answer)
Explanation: ***Unconscious patients*** - The **Doll's Eye Reflex**, also known as the **oculocephalic reflex**, is a brainstem reflex used to assess brainstem function in **comatose or unconscious patients** [1]. - It is positive if the eyes move in the opposite direction to the head turn, indicating intact brainstem pathways [1]. *Hemiplegic* - **Hemiplegia** refers to paralysis on one side of the body, often due to stroke or brain injury. - While it can be associated with altered consciousness, the Doll's Eye Reflex specifically tests brainstem integrity in unconscious states, not the motor deficits of hemiplegia itself. *Paraplegic* - **Paraplegia** is paralysis affecting the lower half of the body. - This condition primarily involves spinal cord damage and does not directly relate to the assessment of brainstem function using the Doll's Eye Reflex. *Cerebral palsy* - **Cerebral palsy** is a group of disorders affecting movement, muscle tone, or posture, caused by damage to the developing brain. - While individuals with cerebral palsy may have neurological impairments, the Doll's Eye Reflex is not a primary diagnostic or assessment tool for this chronic condition; it is used acutely in unconscious states.
Question 32: In which condition is Serum Amyloid Associated (SAA) protein most commonly found?
- A. Alzheimer's disease
- B. Malignant hypertension
- C. Chronic inflammatory states (Correct Answer)
- D. Chronic renal failure
- E. Acute myocardial infarction
Explanation: ***Chronic inflammatory states*** [1][2] - Serum amyloid-associated protein is elevated in response to **chronic inflammation**, such as in rheumatic diseases and infections [1][2]. - It serves as a **biomarker** indicating systemic inflammation and is part of the **acute-phase response** [1]. *Chronic renal failure* - While renal failure can lead to amyloidosis, it is not a direct cause of serum amyloid-associated protein elevation. - **Renal impairment** is more associated with a decrease in clearance rather than production of amyloid proteins. *Alzheimer's disease* - Although amyloid plaques are a hallmark of Alzheimer's, they are related to **A-beta peptide**, not serum amyloid-associated protein. - Alzheimer's pathology primarily involves **neurodegeneration** rather than inflammatory response. *Malignant hypertension* - Malignant hypertension primarily affects the **vascular system** and does not directly involve the production of serum amyloid-associated protein. - It is characterized by end-organ damage, rather than a state of chronic inflammation. *Chronic inflammatory conditions like RA, TB & leprosy, osteomyelitis, ankylosing spondylitis, IBD, bronchiectasis, some tumors* [1][2] - While these conditions can be associated with systemic inflammation, they are too specific and do not comprehensively encompass the broader concept of **chronic inflammatory states**. - This option fails to highlight that serum amyloid-associated protein is a marker for **various chronic inflammatory states** beyond just those listed [1].
Question 33: In evaluation of a case of immotile nasal cilia, which of the following investigations should prove useful?
- A. Rhinogram
- B. Sweat sodium levels
- C. Nitric oxide test (Correct Answer)
- D. Xray nasal and paranasal sinuses
Explanation: Nitric oxide test - A low nasal nitric oxide (nNO) concentration is a key diagnostic criterion for Primary Ciliary Dyskinesia (PCD), a genetic disorder characterized by immotile or dyskinetic cilia [1]. - Nasal NO is significantly reduced in PCD patients due to impaired ciliary function, making this test highly useful for screening. *Rhinogram* - A rhinogram is a radiographic imaging technique primarily used to visualize the nasal cavity and paranasal sinuses, often to detect structural abnormalities or foreign bodies. - It does not directly assess ciliary function or provide information about ciliary motility. *Sweat sodium levels* - Elevated sweat chloride or sodium levels are the diagnostic hallmark of cystic fibrosis, a genetic condition primarily affecting mucus production. - While cystic fibrosis can cause respiratory symptoms, it does not directly lead to immotile nasal cilia in the same manner as PCD. *Xray nasal and paranasal sinuses* - An X-ray of the nasal and paranasal sinuses can reveal structural issues, such as sinus opacification or polyps, which may accompany ciliary dysfunction. - However, it does not provide direct information about the motility or structural integrity of the cilia themselves.
Question 34: Saddle nose deformity is seen in?
- A. Primary Syphilis
- B. Secondary Syphilis
- C. Tertiary Syphilis (Correct Answer)
- D. Lupus Vulgaris
Explanation: ***Tertiary Syphilis*** - **Saddle nose deformity** is a characteristic late manifestation of **tertiary syphilis** due to destructive lesions (gummas) affecting the nasal cartilage and bone [1], [2]. - It results from the **collapse of the nasal bridge**, leading to a flattened appearance [2]. *Primary Syphilis* - Characterized by a **chancre**, a painless ulcer, usually at the site of infection [1]. - This stage does not involve destructive lesions of the nose. *Secondary Syphilis* - Presents with a **widespread rash**, lymphadenopathy, and mucous patches [1]. - While systemic, it typically does not cause structural damage like saddle nose deformity. *Lupus Vulgaris* - This is a **cutaneous form of tuberculosis**, characterized by chronic, destructive skin lesions. - While it can cause facial disfigurement, saddle nose deformity is not a typical feature of lupus vulgaris.
Question 35: Which of the following statements regarding Pertussis is INCORRECT?
- A. The drug of choice is Erythromycin.
- B. Cerebellar ataxia is a known complication. (Correct Answer)
- C. Some infections may be subclinical.
- D. The most infective stage is the catarrhal stage.
Explanation: ***Cerebellar ataxia is a known complication.*** - **Cerebellar ataxia** is not a typical or known complication of pertussis. Complications usually involve the respiratory, neurological (e.g., seizures, encephalopathy due to hypoxia), and nutritional systems due to severe coughing. - While neurological complications can occur, **ataxia** specifically is not frequently sighted in the context of pertussis. *Some infections may be subclinical.* - Some individuals, especially those partially immunized or older, can experience **subclinical or atypical infections** with pertussis, often presenting as a mild cough. - This characteristic makes it difficult to control the spread of the disease as infected individuals may not be recognized. *The most infective stage is the catarrhal stage.* - The **catarrhal stage**, characterized by non-specific cold-like symptoms, is the most contagious phase because bacterial shedding is highest. - During this stage, symptoms are mild and often indistinguishable from a common cold, leading to widespread transmission before diagnosis. *The drug of choice is Erythromycin.* - **Erythromycin**, or other macrolides like azithromycin or clarithromycin, are the drugs of choice for treating pertussis. - These antibiotics are most effective when administered early in the **catarrhal stage** to reduce disease severity and prevent transmission.
Question 36: Post-tubercular bronchiectasis is most commonly seen with
- A. Pertussis
- B. Cystic fibrosis
- C. Kartagener syndrome
- D. Tuberculosis (Correct Answer)
Explanation: ***Tuberculosis*** - **Tuberculosis (TB)**, particularly childhood TB, is a leading cause of post-infectious bronchiectasis, especially in regions with high TB prevalence [1]. - The inflammatory and destructive processes associated with TB infection in the lungs can lead to irreversible dilation and damage of the bronchi [1]. *Pertussis* - While **pertussis** can cause severe respiratory inflammation and chronic cough, it is a less common cause of widespread, irreversible bronchiectasis compared to tuberculosis [1]. - The damage caused by pertussis is typically more acute and less likely to lead to long-term structural changes like those seen in post-tubercular bronchiectasis. *Cystic fibrosis* - **Cystic fibrosis** is a genetic disorder that causes thick, sticky mucus to build up in the lungs, leading to chronic infections and bronchiectasis [1]. - However, post-tubercular bronchiectasis refers specifically to bronchiectasis developing *after* a tuberculosis infection, not as a primary genetic condition. *Kartagener syndrome* - **Kartagener syndrome** is a genetic disorder characterized by defects in ciliary function, leading to impaired mucociliary clearance and recurrent respiratory infections, which can result in bronchiectasis [1]. - Similar to cystic fibrosis, this is a primary genetic cause of bronchiectasis, distinct from bronchiectasis occurring as a sequela of tuberculosis.
Question 37: Central bronchiectasis is seen with
- A. Cystic fibrosis (Correct Answer)
- B. Tuberculosis
- C. Bronchogenic carcinoma
- D. Cystic Adenomatoid Malformation (CAM)
Explanation: ***Cystic fibrosis*** - **Cystic Fibrosis (CF)** is a genetic disorder commonly associated with **central bronchiectasis**, particularly affecting the upper lobes and central airways. - The abnormal mucus production in CF leads to chronic infection, inflammation, and eventual **dilation of the bronchi**, prominent in the central regions. *Bronchogenic carcinoma* - **Bronchogenic carcinoma** can cause **post-obstructive bronchiectasis** distal to the tumor due to airway obstruction and reduced clearance. - However, the bronchiectasis tends to be **localized** to the segment supplied by the obstructed bronchus, rather than being diffusely central. *Tuberculosis* - **Tuberculosis (TB)** can lead to bronchiectasis, often affecting the **upper lobes** and causing localized airway damage. - While TB can cause changes in the bronchi, it is typically linked with **focal or segmental bronchiectasis** resulting from inflammatory destruction, not diffuse central bronchiectasis like CF. *Cystic Adenomatoid Malformation (CAM)* - **Cystic Adenomatoid Malformation (CAM)** is a **congenital lung lesion** with abnormal airway development, but it does not primarily involve bronchiectasis. - CAM is characterized by **cystic structures** or abnormal lung tissue, not the permanent dilation of the bronchi seen in typical bronchiectasis.
Question 38: Which of the following is seen in sarcoidosis
- A. Decreased calcium levels in the blood (Hypocalcemia)
- B. Increased phosphate levels in the blood (Hyperphosphatemia)
- C. Increased calcium levels in the blood (Hypercalcemia) (Correct Answer)
- D. Decreased phosphate levels in the blood (Hypophosphatemia)
Explanation: ***Increased calcium levels in the blood (Hypercalcemia)*** - In sarcoidosis, activated macrophages in granulomas produce **1-alpha hydroxylase**, which converts **25-hydroxyvitamin D to 1,25-dihydroxyvitamin D (calcitriol)** [1]. - This increased calcitriol leads to enhanced intestinal **calcium absorption** and occasional bone resorption, resulting in **hypercalcemia** [1]. *Decreased calcium levels in the blood (Hypocalcemia)* - **Hypocalcemia** is not characteristic of sarcoidosis; the disease typically involves dysregulated vitamin D metabolism causing elevated, not decreased, calcium [1]. - Conditions like **hypoparathyroidism** or **vitamin D deficiency** (unrelated to the sarcoidosis pathogenesis) would cause hypocalcemia. *Increased phosphate levels in the blood (Hyperphosphatemia)* - **Hyperphosphatemia** is not a feature of sarcoidosis. Calcium and phosphate levels often have an inverse relationship, so with hypercalcemia, phosphate levels tend to be normal or slightly decreased due to suppression of parathyroid hormone. - Hyperphosphatemia is more commonly associated with **renal failure** or certain **endocrine disorders**. *Decreased phosphate levels in the blood (Hypophosphatemia)* - While **hypophosphatemia** can occur in conditions with high vitamin D activity (as increased active vitamin D can promote renal phosphate excretion), it is not the primary or most notable electrolyte disturbance specifically linked to sarcoidosis. - **Hypercalcemia** is the more consistently observed electrolyte abnormality in sarcoidosis related to ectopic vitamin D production [1].
Question 39: Aspirin sensitive asthma is associated with:
- A. Extrinsic asthma
- B. Associated with nasal polyp (Correct Answer)
- C. Obesity
- D. Usually associated with urticaria
Explanation: **Associated with nasal polyp** - **Aspirin-exacerbated respiratory disease (AERD)**, also known as aspirin-sensitive asthma, is characterized by a triad of **asthma**, **rhinosinusitis with nasal polyposis**, and respiratory reactions to **aspirin** and other NSAIDs [1]. - The presence of **nasal polyps** is a key clinical feature differentiating AERD from other forms of asthma [1]. *Obesity* - While **obesity** can exacerbate asthma severity, it is not specifically associated with the pathogenesis or diagnosis of **aspirin-sensitive asthma**. - It is a general risk factor for various health issues, including more severe asthma, but lacks specificity for AERD. *Extrinsic asthma* - **Extrinsic asthma** (allergic asthma) is typically triggered by environmental allergens and involves an **IgE-mediated response** [2]. - AERD is considered a **non-allergic** or **intrinsic asthma** phenotype, as it is not triggered by traditional allergens but by pharmacologic agents [1]. *Usually associated with urticaria* - **Urticaria** (hives) can be a feature of aspirin and NSAID sensitivity, particularly in some forms of **NSAID-induced urticaria/angioedema**. - However, the classic respiratory reactions of **aspirin-sensitive asthma** (bronchospasm, rhinitis) are distinct from urticarial reactions and typically do not present with primary urticaria.
Question 40: Which of the following is the common cause of respiratory failure type 2 ?
- A. Chronic bronchitis exacerbation (Correct Answer)
- B. Acute attack asthma
- C. ARDS
- D. Pneumonia
Explanation: ***Chronic bronchitis exacerbation*** - **Chronic bronchitis** is a common cause of **Type 2 respiratory failure**, characterized by **hypercapnia** (elevated CO2) due to impaired alveolar ventilation [1]. - An exacerbation worsens **airflow obstruction** and leads to increased work of breathing and CO2 retention [1]. *Acute attack asthma* - While severe asthma can cause respiratory failure, it typically presents initially as **Type 1 (hypoxemic)**, with severe bronchospasm and V/Q mismatch [2]. - **Hypercapnia** in asthma is a sign of **severe, impending respiratory collapse** rather than the primary cause of respiratory failure. *ARDS* - **Acute Respiratory Distress Syndrome (ARDS)** is a classic cause of **Type 1 (hypoxemic) respiratory failure**, characterized by widespread inflammation and fluid accumulation in the lungs [2]. - ARDS primarily involves impaired oxygenation rather than CO2 elimination issues, unless it progresses to severe stages with significant muscle fatigue. *Pneumonia* - **Pneumonia** predominantly causes **Type 1 (hypoxemic) respiratory failure** due to consolidation and V/Q mismatch in affected lung areas, leading to impaired oxygen diffusion [2]. - While severe, widespread pneumonia can eventually lead to ventilatory failure, its initial and primary impact is on oxygenation.