Forensic Medicine
1 questionsWhat substance is measured in the vitreous humor to estimate the time since death?
NEET-PG 2012 - Forensic Medicine NEET-PG Practice Questions and MCQs
Question 711: What substance is measured in the vitreous humor to estimate the time since death?
- A. Sodium
- B. Potassium (Correct Answer)
- C. Proteins
- D. Chloride
Explanation: ***Potassium*** - **Potassium** concentration in the vitreous humor increases predictably after death due to the breakdown of cellular membranes and passive diffusion from cells. - This consistent post-mortem rise makes it a reliable marker for estimating the **post-mortem interval** (PMI) or time since death. *Sodium* - While sodium is present in the vitreous humor, its post-mortem changes are not as consistent or predictable as potassium for estimating the **time since death**. - Sodium levels tend to decrease slightly after death, but this decline is influenced by various factors and is less reliable for **PMI determination**. *Proteins* - **Proteins** are generally stable in the vitreous humor for some time post-mortem, but their levels do not show a consistent or predictable change that can be used to accurately estimate the **time since death**. - Measuring protein levels is more useful in assessing specific eye pathologies rather than **PMI**. *Chloride* - **Chloride** concentrations in the vitreous humor exhibit post-mortem changes, but like sodium, they are not as precise or reliable as potassium for estimating the **post-mortem interval**. - Its diffusion out of the vitreous humor can be more variable and less consistently linear than potassium's influx.
Internal Medicine
1 questionsWhat condition is caused by the intake of exogenous steroids?
NEET-PG 2012 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 711: What condition is caused by the intake of exogenous steroids?
- A. Addison's disease
- B. Cushing's syndrome (Correct Answer)
- C. Pheochromocytoma
- D. Conn's syndrome
Explanation: ***Cushing's syndrome*** - **Exogenous steroid intake** is the most common cause of Cushing's syndrome, leading to symptoms associated with **excess cortisol** [1]. - This occurs because the steroids mimic the effects of **cortisol**, suppressing the body's natural production and leading to its characteristic signs and symptoms [2]. *Addison's disease* - This condition is characterized by **adrenal insufficiency**, meaning the adrenal glands produce too little **cortisol** and often **aldosterone**. - It is typically caused by autoimmune destruction of the adrenal glands, not by exogenous steroid intake. *Pheochromocytoma* - This is a rare tumor of the **adrenal medulla** that causes the overproduction of **catecholamines** (epinephrine and norepinephrine). - Symptoms include sudden, severe episodes of hypertension, palpitations, and sweating, unrelated to steroid intake. *Conn's syndrome* - Also known as **primary hyperaldosteronism**, this condition involves the overproduction of **aldosterone** by the adrenal glands. - It typically results in hypertension and hypokalemia and is not directly caused by exogenous steroid administration.
Pathology
1 questionsPerivascular lymphocytes & microglial nodules are seen in -
NEET-PG 2012 - Pathology NEET-PG Practice Questions and MCQs
Question 711: Perivascular lymphocytes & microglial nodules are seen in -
- A. HIV encephalitis (Correct Answer)
- B. CMV meningitis
- C. Bacterial meningitis
- D. Multiple sclerosis
Explanation: ***HIV encephalitis*** - **Perivascular lymphocytes** and **microglial nodules** are the characteristic histopathological hallmarks of **HIV encephalitis (HIV-associated dementia complex)** [1][2]. - Microglial nodules are formed by activated microglia and macrophages, often accompanied by **multinucleated giant cells** (the classic triad) [2]. - These features reflect chronic CNS inflammation and neuronal damage caused by HIV infection. *CMV meningitis* - Cytomegalovirus (CMV) infection in immunocompromised patients causes meningoencephalitis with characteristic **intranuclear ("owl's eye") inclusion bodies** and necrotizing inflammation. - The histological pattern differs from the microglial nodules and perivascular lymphocytes seen in HIV encephalitis. *Bacterial meningitis* - Characterized by prominent **neutrophilic infiltrate** in the subarachnoid space, fibrinopurulent exudate, and potential vasculitis. - Acute bacterial meningitis does not show the lymphocytic and microglial nodular pattern characteristic of viral encephalitis. *Multiple sclerosis* - An autoimmune demyelinating disease with **perivenular demyelinating plaques** containing lymphocytes and macrophages. - While perivascular inflammation occurs, **microglial nodules** are not a characteristic feature; instead, MS shows demyelination with reactive gliosis. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Central Nervous System, p. 1278. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Manifestations Of Central And Peripheral Nervous System Disease, pp. 711-712.
Pharmacology
7 questionsWhat is a key difference between fosphenytoin and phenytoin?
Which of the following is NOT a mechanism of action of theophylline in bronchial asthma?
Omalizumab is primarily used in the treatment of which condition?
Which of the following is a selective serotonin and norepinephrine reuptake inhibitor?
Which steroid has the maximum mineralocorticoid activity?
Which statin is considered most potent based on mg-to-mg LDL reduction capability?
Which of the following antiepileptic drugs is most classically associated with causing hirsutism?
NEET-PG 2012 - Pharmacology NEET-PG Practice Questions and MCQs
Question 711: What is a key difference between fosphenytoin and phenytoin?
- A. Can be used in absence seizures
- B. Can be mixed with saline (Correct Answer)
- C. Can be given orally
- D. It is the drug of choice for myoclonic seizures
Explanation: **Can be mixed with saline** - **Fosphenytoin** is a water-soluble prodrug that is converted to phenytoin in the body; its solubility allows it to be **mixed with saline** solutions for intravenous administration, minimizing the risk of precipitation. - Unlike phenytoin, fosphenytoin's formulation avoids the need for propylene glycol, which is associated with adverse cardiovascular effects and makes phenytoin incompatible with saline. *Can be used in absence seizures* - Neither **fosphenytoin nor phenytoin** is effective for treating **absence seizures**, and they can sometimes worsen them. - **Ethosuximide** or **valproic acid** are the drugs of choice for absence seizures. *Can be given orally* - While **phenytoin** is commonly available in oral forms (capsules, chewable tablets, suspension), **fosphenytoin** is primarily designed for **parenteral administration** (intravenous or intramuscular). - Fosphenytoin is a prodrug that is rapidly converted to phenytoin *in vivo*, but it is not typically available or indicated for direct oral administration. *It is the drug of choice for myoclonic seizures* - Neither **fosphenytoin nor phenytoin** is the drug of choice for **myoclonic seizures**; they can exacerbate this type of seizure. - **Valproic acid** and **levetiracetam** are preferred treatments for myoclonic seizures due to their broader spectrum of activity.
Question 712: Which of the following is NOT a mechanism of action of theophylline in bronchial asthma?
- A. Adenosine receptor antagonism
- B. Increased histone deacetylation
- C. Phosphodiesterase inhibition
- D. Beta-2 receptor stimulation (Correct Answer)
Explanation: ***Beta-2 receptor stimulation*** - Theophylline is a **non-selective phosphodiesterase inhibitor** and an **adenosine receptor antagonist**, but it does not directly stimulate beta-2 receptors. - **Beta-2 receptor agonists** like salbutamol or formoterol are the medications that work by stimulating these receptors to cause bronchodilation. *Phosphodiesterase inhibition* - Theophylline inhibits **phosphodiesterase enzymes**, leading to an increase in intracellular **cAMP** levels. - This increase in **cAMP** promotes bronchodilation by relaxing airway smooth muscle. *Adenosine receptor antagonism* - Theophylline acts as an antagonist at **adenosine receptors**, particularly A1 and A2B. - Antagonism of adenosine receptors can reduce bronchoconstriction and inflammatory mediator release, contributing to its anti-asthmatic effects. *Increased histone deacetylation* - Theophylline, particularly at lower concentrations, increases the activity of **histone deacetylase (HDAC)**. - This action helps to **repress inflammatory gene expression**, which is a unique anti-inflammatory mechanism separate from its bronchodilatory effects.
Question 713: Omalizumab is primarily used in the treatment of which condition?
- A. Breast carcinoma
- B. Asthma (Correct Answer)
- C. Rheumatoid arthritis
- D. Chronic obstructive pulmonary disease (COPD)
Explanation: ***Asthma*** - **Omalizumab** is a **monoclonal antibody** that targets and binds to **immunoglobulin E (IgE)**, preventing it from binding to mast cells and basophils. - By reducing free IgE, omalizumab helps to prevent the release of inflammatory mediators, thereby **reducing allergic reactions and asthma symptoms**, particularly in patients with severe persistent allergic asthma. *Breast carcinoma* - **Omalizumab** is not indicated for the treatment of **breast carcinoma**; treatments for breast cancer typically involve chemotherapy, radiation, surgery, and targeted therapies specific to cancer cells. - Targeted therapies for breast cancer often focus on hormone receptors (e.g., **estrogen receptor**) or growth factor receptors (e.g., **HER2**), not IgE. *Rheumatoid arthritis* - **Omalizumab** is not used for **rheumatoid arthritis (RA)**; RA is an autoimmune disease primarily involving **T-cells and cytokines** like **TNF-alpha** and **IL-6**. - Treatment for RA typically includes **DMARDs** (disease-modifying antirheumatic drugs) and **biological agents** that target specific inflammatory pathways (e.g., **adalimumab**, **etanercept**). *Chronic obstructive pulmonary disease (COPD)* - **Omalizumab** is not indicated for **COPD**, which is primarily characterized by chronic inflammation of the airways and **emphysema**, largely caused by smoking. - COPD management focuses on bronchodilators, corticosteroids, and oxygen therapy, with no role for IgE-targeting therapy.
Question 714: Which of the following is a selective serotonin and norepinephrine reuptake inhibitor?
- A. Fluoxetine
- B. Venlafaxine (Correct Answer)
- C. Sertraline
- D. Aripiprazole
Explanation: ***Venlafaxine*** - **Venlafaxine** is a commonly used antidepressant that inhibits the reuptake of both **serotonin** and **norepinephrine**, making it an SNRI. - Its dual mechanism of action can be effective for a broad range of depressive and anxiety disorders. *Fluoxetine* - **Fluoxetine** is a **selective serotonin reuptake inhibitor (SSRI)**, primarily affecting serotonin levels in the brain. - It does not significantly inhibit norepinephrine reuptake and, thus, is not classified as an SNRI. *Sertraline* - **Sertraline** is another widely prescribed antidepressant that is also a **selective serotonin reuptake inhibitor (SSRI)**. - It works mainly by increasing serotonin availability in the synaptic cleft. *Aripiprazole* - **Aripiprazole** is an **atypical antipsychotic** medication, often used as an adjunct therapy for depression, but its primary mechanism is partial agonism at dopamine D2 and serotonin 5-HT1A receptors, and antagonism at serotonin 5-HT2A receptors. - It is not classified as a selective serotonin and norepinephrine reuptake inhibitor.
Question 715: Which steroid has the maximum mineralocorticoid activity?
- A. Fludrocortisone (Correct Answer)
- B. DOCA
- C. Prednisolone
- D. Triamcinolone
Explanation: ***Fludrocortisone*** - **Fludrocortisone** is a synthetic corticosteroid specifically designed to have potent **mineralocorticoid activity**, with significant sodium-retaining properties. - Its high affinity for **mineralocorticoid receptors** distinguishes it from other steroids and makes it effective in treating conditions like **Addison's disease** and **postural orthostatic tachycardia syndrome (POTS)** due to its ability to retain sodium and water. *DOCA (Deoxycorticosterone acetate)* - While **DOCA** does possess significant **mineralocorticoid activity** and was historically used for this purpose, **fludrocortisone** is generally considered to have a stronger and more sustained effect in clinical practice. - **DOCA's** mineralocorticoid potency is substantial but slightly less than that of **fludrocortisone** when compared on a weight basis for equivalent sodium retention. *Prednisolone* - **Prednisolone** is primarily a **glucocorticoid** with potent anti-inflammatory and immunosuppressive effects. - It has minimal to negligible **mineralocorticoid activity** and is not used for salt retention purposes. *Triamcinolone* - **Triamcinolone** is a potent **glucocorticoid** with a long duration of action and is known for its strong anti-inflammatory properties. - It has virtually no **mineralocorticoid activity**, making it unsuitable for conditions requiring sodium retention.
Question 716: Which statin is considered most potent based on mg-to-mg LDL reduction capability?
- A. Simvastatin
- B. Pravastatin
- C. Rosuvastatin (Correct Answer)
- D. Atorvastatin
Explanation: ***Rosuvastatin*** - **Rosuvastatin** is known for its high potency, achieving significant **LDL-C reduction** at relatively low doses. - It is often considered the most potent statin on a **milligram-to-milligram basis**. *Simvastatin* - **Simvastatin** is a moderate-intensity statin, not as potent as rosuvastatin or atorvastatin in reducing LDL-C. - While effective, it typically requires higher doses to achieve comparable **LDL-C reductions** seen with high-potency statins. *Pravastatin* - **Pravastatin** is a hydrophilic statin, generally considered to be of lower potency compared to other statins like rosuvastatin and atorvastatin. - It is often used in patients with **hepatic dysfunction** due to its different metabolic profile but offers less aggressive **LDL-C reduction**. *Atorvastatin* - **Atorvastatin** is a high-intensity statin, very effective in reducing LDL-C, and often used for aggressive lipid lowering. - While highly potent, **atorvastatin** is generally considered slightly less potent than **rosuvastatin** on a mg-to-mg basis, though both are used for high-intensity lipid therapy.
Question 717: Which of the following antiepileptic drugs is most classically associated with causing hirsutism?
- A. Phenytoin (Correct Answer)
- B. Valproate
- C. Carbamazepine
- D. Phenobarbitone
Explanation: ***Phenytoin*** - **Phenytoin** is the **most classically associated** antiepileptic drug with **hirsutism**, which is abnormal/excessive growth of hair [1]. - The mechanism involves changes in **androgen metabolism** and stimulation of hair follicle growth. - Other cosmetic side effects include **gingival hyperplasia** and **coarsening of facial features** [1].*Valproate* - Valproate can paradoxically cause both **hair loss (alopecia)** and **hirsutism**, particularly in women and children. - However, phenytoin has a **stronger and more classical association** with hirsutism. - Valproate is also known for **weight gain**, **hepatotoxicity**, **pancreatitis**, and **teratogenicity**.*Carbamazepine* - Carbamazepine's common side effects include **drowsiness**, **dizziness**, **diplopia**, and **hyponatremia**. - It is not classically linked to **hirsutism** as a prominent adverse effect. - Can cause **agranulocytosis** and **Stevens-Johnson syndrome** in rare cases.*Phenobarbitone* - Phenobarbitone is an older antiepileptic drug associated with **sedation**, **cognitive impairment**, and **dependence**. - It does not commonly cause **hirsutism**. - Also causes **enzyme induction** leading to multiple drug interactions.