In a patient with acute cholecystitis, referred pain to the shoulder is known as
In Marfan's syndrome, Aortic aneurysm occurs most commonly in:
In which condition is paradoxical splitting of the second heart sound observed?
Which of the following electrolyte imbalances is least likely to be observed in Chronic Renal Failure (CRF)?
What is the best treatment for anemia in patients with Chronic Renal Failure (CRF)?
An adult hypertensive male presented with sudden onset severe headache and vomiting. On examination, there is marked neck rigidity and no focal neurological deficit was found. The symptoms are most likely due to:
What is the most characteristic cerebrospinal fluid (CSF) finding in viral meningitis?
Which of the following statements is MOST accurate regarding herpes encephalitis?
Esophageal manometry is useful in diagnosing all of the following conditions EXCEPT:
Tall T waves on ECG are seen in:
NEET-PG 2012 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 91: In a patient with acute cholecystitis, referred pain to the shoulder is known as
- A. Murphy's sign
- B. Gray Turner sign
- C. Boas' sign (Correct Answer)
- D. Cullen's sign
Explanation: ***Boas' sign*** - **Boas' sign** refers to the presence of hyperesthesia below the right scapula, which can also manifest as referred pain to the **right shoulder** or back [1]. - This symptom in acute cholecystitis is due to the **irritation** of the **phrenic nerve**, which shares sensory pathways with the shoulder region. *Murphy's sign* - **Murphy's sign** is elicited by asking the patient to exhale, then placing the examiner's hand below the costal margin on the right mid-clavicular line, and then asking the patient to inhale deeply [1]. - A positive sign is indicated by a sudden cessation of inspiration due to pain, which is specific for **acute cholecystitis** and not referred shoulder pain [1]. *Gray Turner sign* - The **Gray Turner sign** involves ecchymosis or discoloration of the flanks. - It is a severe indicator of **retroperitoneal hemorrhage**, often associated with acute pancreatitis, not cholecystitis [2]. *Cullen's sign* - **Cullen's sign** presents as periumbilical ecchymosis or discoloration around the navel. - This sign is also indicative of **retroperitoneal hemorrhage**, typically seen in serious conditions like ruptured ectopic pregnancy or acute pancreatitis.
Question 92: In Marfan's syndrome, Aortic aneurysm occurs most commonly in:
- A. Ascending aorta (Correct Answer)
- B. Descending aorta
- C. Abdominal aorta
- D. Arch of aorta
Explanation: ***Ascending aorta*** - The **ascending aorta** is the most common site for aortic aneurysm and dissection in Marfan syndrome due to cystic medial degeneration weakening the vessel wall [1]. - This predisposition is linked to defects in the **fibrillin-1 gene (FBN1)**, severely impacting the structural integrity of the arterial media primarily in the ascending aorta [1]. *Descending aorta* - While possible, **descending aortic** involvement is less common than ascending aortic involvement in Marfan syndrome [2]. - Aneurysms here are more frequently associated with atherosclerosis or other connective tissue disorders. *Abdominal aorta* - **Abdominal aortic aneurysms** are relatively rare in Marfan syndrome and are more typically seen in older patients with atherosclerosis [3]. - The disease primarily affects the elastic tissue content, which is most abundant in the proximal aorta. *Arch of aorta* - Aortic arch aneurysms can occur, but they are still less frequent than those in the **ascending aorta** as the primary initial site of dilation and dissection in Marfan syndrome. - Arch involvement often represents an extension of a more proximal ascending aortic pathology.
Question 93: In which condition is paradoxical splitting of the second heart sound observed?
- A. Right Bundle Branch Block (RBBB)
- B. Left Bundle Branch Block (LBBB) (Correct Answer)
- C. Ventricular Septal Defect (VSD)
- D. Atrial Septal Defect (ASD)
Explanation: ***Left Bundle Branch Block (LBBB)*** - In LBBB, the **left ventricle** depolarizes and contracts *after* the right ventricle, causing the **aortic valve (A2)** to close *after* the **pulmonic valve (P2)** [1]. - During inspiration, right ventricular ejection time is prolonged, which further delays P2. However, in LBBB, A2 is already delayed, and the inspiratory delay of P2 can bring P2 closer to A2, or even cause them to merge, making the splitting *less wide* or *disappear* on inspiration, which is paradoxical. *Right Bundle Branch Block (RBBB)* - RBBB causes a **delay in right ventricular depolarization**, leading to a **delayed P2** (pulmonic valve closure). - This typically results in **wide and fixed splitting of S2**, where the splitting persists during expiration and widens further with inspiration, which is not paradoxical. *Ventricular Septal Defect (VSD)* - A VSD can cause a **loud holosystolic murmur** and may lead to increased pulmonary blood flow. - While it can affect the timing of heart sounds, it does not typically cause paradoxical splitting of S2. *Atrial Septal Defect (ASD)* - An ASD causes a **left-to-right shunt**, leading to chronic volume overload of the right ventricle and increased pulmonary blood flow. - This often results in a **widely fixed splitting of S2**, where the split between A2 and P2 is constant regardless of respiration, which is different from paradoxical splitting.
Question 94: Which of the following electrolyte imbalances is least likely to be observed in Chronic Renal Failure (CRF)?
- A. Hyperkalemia
- B. Hyperphosphatemia
- C. Hypercalcemia (Correct Answer)
- D. Hypocalcemia
Explanation: ***Hypercalcemia*** - In **chronic renal failure (CRF)**, the kidneys' inability to activate vitamin D leads to impaired calcium absorption and **hypocalcemia** [1], [2]. - Additionally, the kidneys fail to excrete phosphate, leading to **hyperphosphatemia**, which further exacerbates hypocalcemia by forming calcium-phosphate precipitates [1]. *Hyperkalemia* - **Hyperkalemia** is a common and serious complication of CRF due to the kidneys' impaired ability to excrete **potassium**. - This is exacerbated by conditions like **metabolic acidosis** and certain medications. *Hyperphosphatemia* - In CRF, the kidneys are unable to adequately excrete **phosphate**, leading to an accumulation of **phosphate** in the blood [1]. - This condition directly contributes to **secondary hyperparathyroidism** and bone disease [1], [2]. *Hypocalcemia* - **Hypocalcemia** is very common in CRF, primarily due to decreased production of **calcitriol (active vitamin D)** by the failing kidneys [2]. - Reduced calcitriol leads to lower intestinal **calcium absorption** and impaired bone mineralization [1].
Question 95: What is the best treatment for anemia in patients with Chronic Renal Failure (CRF)?
- A. Oral Iron Therapy
- B. Erythropoietin Stimulating Agents (Correct Answer)
- C. Blood transfusion
- D. Androgenic Steroids
Explanation: ***Erythropoietin Stimulating Agents*** - **Erythropoietin Stimulating Agents (ESAs)** are the cornerstone of anemia treatment in CRF because the primary cause of anemia in these patients is inadequate production of **endogenous erythropoietin** by the damaged kidneys [1]. - ESAs stimulate the bone marrow to produce red blood cells, effectively reversing the anemia and improving symptoms like fatigue and exercise intolerance [1]. *Oral Iron Therapy* - While **iron deficiency** often coexists with **anemia of chronic disease** in CRF patients, oral iron alone is usually insufficient to correct the anemia; it only addresses the iron component. - Many CRF patients have **functional iron deficiency** due to chronic inflammation, which impairs iron utilization, making oral iron less effective even with adequate stores. *Blood transfusion* - **Blood transfusions** provide a rapid increase in hemoglobin but are not the preferred long-term treatment for anemia in CRF due to risks of **iron overload**, **alloreactions**, and potential sensitization, which can complicate future transplantation. - Transfusions are typically reserved for acute, severe anemia or specific circumstances where ESAs are ineffective or contraindicated. *Androgenic Steroids* - **Androgenic steroids** can stimulate erythropoiesis, but their use is limited due to significant side effects such as **hepatotoxicity**, **virilization**, and **cardiac complications**, making them a less favorable option compared to ESAs. - They are considered a secondary or tertiary option, often in patients unresponsive to primary treatments or when other options are exhausted.
Question 96: An adult hypertensive male presented with sudden onset severe headache and vomiting. On examination, there is marked neck rigidity and no focal neurological deficit was found. The symptoms are most likely due to:
- A. Subarachnoid hemorrhage (Correct Answer)
- B. Intracerebral hemorrhage
- C. Cerebral ischemia
- D. Bacterial meningitis
Explanation: ***Subarachnoid hemorrhage*** - The sudden onset of a **"thunderclap" headache**, vomiting, and **neck rigidity** in a hypertensive patient are classic signs of subarachnoid hemorrhage [1]. - The absence of focal neurological deficits is common, as the bleeding is often in the subarachnoid space rather than directly in brain tissue. *Intracerebral hemorrhage* - While it can cause sudden headache and vomiting, an **intracerebral hemorrhage** would typically present with **focal neurological deficits** corresponding to the affected brain region. - Neck rigidity is less common unless there's significant mass effect or ventricular involvement. *Cerebral ischemia* - **Cerebral ischemia** (e.g., ischemic stroke) usually manifests with **focal neurological deficits** (e.g., weakness, aphasia), often without a severe headache or neck rigidity [2]. - Headache, if present, is usually less severe and not described as "thunderclap." *Bacterial meningitis* - **Bacterial meningitis** presents with headache, fever, and neck rigidity [1], but the onset is typically **gradual** over hours to days, not sudden. - While vomiting can occur, the acute, thunderclap nature linked to hypertension points away from infection as the primary cause.
Question 97: What is the most characteristic cerebrospinal fluid (CSF) finding in viral meningitis?
- A. Lymphocytic pleocytosis in CSF (Correct Answer)
- B. WBC count typically less than 1000/mL
- C. Glucose levels normal or slightly decreased
- D. Protein levels normal or slightly increased
Explanation: ***Lymphocytic pleocytosis in CSF*** - **Lymphocytic pleocytosis**, meaning an increase in lymphocytes in the CSF, is the hallmark of **viral meningitis**, reflecting the immune response to the viral pathogen. [1] - While other CSF parameters can be altered, the presence of predominantly lymphocytes is the most reliable distinguishing feature from bacterial meningitis. [1] *WBC count typically less than 1000/mL* - This statement is generally true for viral meningitis, as the **WBC count** is usually lower than in bacterial meningitis. - However, it is not the *most characteristic* finding because bacterial meningitis can sometimes present with a WBC count under 1000/mL, especially early in the disease, and the *predominance* of lymphocytes is more specific to viral infection. *Glucose levels normal or slightly decreased* - **Normal glucose levels** are typical in viral meningitis, but they can be slightly decreased in a minority of cases. - This finding is not as characteristic as lymphocytic pleocytosis because significantly decreased glucose levels are more indicative of **bacterial or fungal meningitis**. *Protein levels normal or slightly increased* - **Protein levels** in viral meningitis are often normal or mildly elevated, usually not exceeding **100-150 mg/dL**. - While consistent with viral meningitis, this finding is less specific than lymphocytic pleocytosis, as protein levels can also be elevated in other conditions, including early bacterial meningitis.
Question 98: Which of the following statements is MOST accurate regarding herpes encephalitis?
- A. Focal neurological symptoms are common.
- B. EEG findings are nonspecific and not diagnostic.
- C. The temporal lobe is commonly involved. (Correct Answer)
- D. MRI is a key diagnostic tool.
Explanation: ***The temporal lobe is commonly involved.*** - **Herpes simplex encephalitis (HSE)** characteristically targets the **temporal lobes** [1] and **orbitofrontal cortex**, leading to specific neurological deficits. - This predilection for the temporal lobes often results in symptoms such as **aphasia**, **seizures**, and **memory disturbances** [1]. *Focal neurological symptoms are common.* - While focal neurological symptoms such as **aphasia**, **hemiparesis**, and **seizures** are indeed common in HSE [1], this statement is less specific than the involvement of the temporal lobe. - The **localization** of the infection to the temporal lobes explains why these focal symptoms are so prevalent [1]. *MRI is a key diagnostic tool.* - **MRI findings**, particularly **T2-weighted** and **FLAIR sequences**, showing **edema** and **hemorrhage** in the temporal lobes and insular cortex, are highly suggestive of HSE. - However, the most definitive diagnostic tool remains the detection of **HSV DNA** in the **cerebrospinal fluid (CSF)** via **PCR**. *EEG findings are nonspecific and not diagnostic.* - **EEG** in HSE often shows **periodic lateralizing epileptiform discharges (PLEDs)** or **focal slowing** primarily over the temporal lobes, which are highly suggestive, although not entirely diagnostic on their own. - These findings can help guide further investigation and support a clinical diagnosis in conjunction with other tests.
Question 99: Esophageal manometry is useful in diagnosing all of the following conditions EXCEPT:
- A. Achalasia (a motility disorder)
- B. Diffuse esophageal spasm (a motility disorder)
- C. Malignancy (not typically diagnosed with this test) (Correct Answer)
- D. Assessment of esophageal motility prior to surgery for GERD
Explanation: ***Malignancy (not typically diagnosed with this test)*** - **Esophageal manometry** evaluates the **motor function** of the esophagus, measuring pressure changes during swallowing. - **Malignancy**, such as esophageal cancer, is primarily diagnosed with **endoscopy with biopsy** and imaging studies, not by assessing motility. *Achalasia (a motility disorder)* - **Esophageal manometry** is the **gold standard** for diagnosing achalasia, characterized by **absent peristalsis** in the esophageal body and **incomplete relaxation of the lower esophageal sphincter (LES)** [1]. - High-resolution manometry shows elevated **integrated relaxation pressure (IRP)** and often pan-esophageal pressurization. *Diffuse esophageal spasm (a motility disorder)* - This condition is also diagnosed by **esophageal manometry**, which reveals simultaneous, **non-peristaltic contractions** of high amplitude, often interspersed with normal peristalsis [1]. - It may also show **premature contractions** and **multiple rapid swallows** triggering spasm. *Assessment of esophageal motility prior to surgery for GERD* - **Manometry** is routinely performed before **anti-reflux surgery (e.g., Nissen fundoplication)** to rule out underlying esophageal motility disorders that could complicate surgery or worsen symptoms post-operatively [1]. - Identifying conditions like **achalasia** or **scleroderma** would contraindicate a standard fundoplication, as dysphagia could worsen [1].
Question 100: Tall T waves on ECG are seen in:
- A. Hyperkalemia (Correct Answer)
- B. Hypokalemia
- C. Hypercalcemia
- D. Hypocalcemia
Explanation: ***Hyperkalemia*** - **Tall, peaked T waves** are a hallmark ECG finding in early to moderate **hyperkalemia**, reflecting altered repolarization due to elevated extracellular potassium [1]. - As potassium levels rise further, other ECG changes may include a **prolonged PR interval**, **widened QRS complex**, and ultimately a **sine wave pattern**, leading to ventricular arrhythmias [1]. *Hypokalemia* - This condition is typically associated with **flattened or inverted T waves**, prominent **U waves**, and a **prolonged QT interval** on the ECG [1]. - The ECG changes in hypokalemia reflect delayed repolarization and increased myocardial instability [1]. *Hypercalcemia* - **Hypercalcemia** is characterized by a **shortened QT interval** on the ECG due to accelerated ventricular repolarization. - T waves, if affected, are usually not tall or peaked but may be wider or slightly less prominent. *Hypocalcemia* - **Hypocalcemia** typically leads to a **prolonged QT interval** on the ECG, primarily due to a lengthened ST segment. - While it can manifest with various T wave morphologies, it does not typically cause the characteristic tall, peaked T waves seen in hyperkalemia.