Internal Medicine
7 questionsWhich of the following is a characteristic feature of primary Sjogren's syndrome?
The most classical symptom of VIPOMA is:
All the following are true about multiple myeloma except for which of the following?
Which of the following is a characteristic feature of myasthenia gravis?
Anomic aphasia is due to defect in
What is the preferred test for confirming H. pylori eradication?
Distal renal tubular acidosis is associated with:
NEET-PG 2012 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 1091: Which of the following is a characteristic feature of primary Sjogren's syndrome?
- A. Can occur in children
- B. Increased complement C4 is associated with thymoma
- C. Can be associated with rheumatoid arthritis
- D. Enlargement of salivary glands (Correct Answer)
Explanation: ***Enlargement of salivary glands*** - **Sjögren's syndrome** is characterized by chronic inflammation of **exocrine glands**, leading to swelling and dysfunction, most notably in the **parotid** and **submandibular glands**. - This glandular enlargement often presents as recurrent or persistent **bilateral swelling** of the major salivary glands. *Can occur in children* - While possible, Sjögren's syndrome is predominantly a disease of **adults**, with incidence peaking in individuals between **40 and 60 years old**. - **Juvenile Sjögren's syndrome** is rare and typically presents with more variable symptoms, making it less of a characteristic feature of the primary disease in the general population. *Increased complement C4 is associated with thymoma* - **Increased complement C4** levels are generally not associated with Sjögren's syndrome; instead, **hypocomplementemia** (low C4) can be seen in some patients, indicating immune complex activity. - **Thymoma** is primarily linked to **myasthenia gravis** and other paraneoplastic syndromes, not a direct or characteristic association with Sjögren's syndrome or C4 levels in this context. *Can be associated with rheumatoid arthritis* - Sjögren's syndrome can be classified as **primary** (occurring alone) or **secondary** (occurring in conjunction with another autoimmune disease). - Its association with **rheumatoid arthritis** defines **secondary Sjögren's syndrome**, meaning it's not a characteristic feature of the *primary* form of the disease itself.
Question 1092: The most classical symptom of VIPOMA is:
- A. Gall stones
- B. Secretory diarrhea (Correct Answer)
- C. Steatorrhea
- D. Flushing
Explanation: The original text cannot be accurately enriched with the provided references to because none of the source materials directly address the pathophysiology or clinical presentation of VIPoma. The available references focus on general gastroenteropancreatic neuroendocrine tumors (NETs) , radiation-induced intestinal damage , arsenic poisoning , gastrointestinal bleeding , and the physiology of taste , but they do not provide the specific confirmation needed for the 'classical symptom' of VIPoma (secretory diarrhea).
Question 1093: All the following are true about multiple myeloma except for which of the following?
- A. Hypercalcemia
- B. Presence of Bence-Jones proteins in urine
- C. Osteolytic bone disease
- D. Chromosomal translocation t(8;14), commonly seen in Burkitt's lymphoma (Correct Answer)
Explanation: ***t(8-14) translocation*** - The **t(8;14) translocation** is not typically associated with multiple myeloma; rather, it is commonly seen in **Burkitt lymphoma** [2]. - Multiple myeloma is primarily linked with chromosomal abnormalities such as **deletions** and **translocations involving different chromosomes**. *Osteolytic bone disease* - A hallmark feature of multiple myeloma, **osteolytic lesions** result from increased osteoclastic activity and are often seen in the skull, spine, and ribs [1]. - Patients frequently present with **bone pain** due to these lesions, which are characteristic of the disease [1]. *Light chain proliferation* - In multiple myeloma, a significant feature is the overproduction of **monoclonal light chains** [1]. - This leads to **light chain disease** or **renal impairment**, further supporting the diagnosis [1]. *Bence-Jones proteins in urine* - The presence of **Bence-Jones proteins**, which are free light chains, is a classic finding in multiple myeloma [1]. - They are often detected in the **urine** and can be used to monitor disease progression or response to treatment [1].
Question 1094: Which of the following is a characteristic feature of myasthenia gravis?
- A. Decreased levels of myosin in muscle fibers
- B. Absence of troponin C in muscle fibers
- C. Increased transmission at the myoneural junction
- D. Presence of antibodies against acetylcholine receptors (Correct Answer)
Explanation: ***Presence of antibodies against acetylcholine receptors*** - **Myasthenia gravis** is an **autoimmune disorder** characterized by the production of **antibodies against acetylcholine receptors** at the neuromuscular junction [1]. - These antibodies block, alter, or destroy the acetylcholine receptors, leading to impaired nerve-to-muscle communication and **muscle weakness** [2]. *Decreased levels of myosin in muscle fibers* - Myosin is a **motor protein** crucial for muscle contraction, and its decreased levels are not a primary feature of myasthenia gravis, but rather other **myopathies** or muscle wasting conditions. - The disease mechanism in myasthenia gravis is primarily at the **neuromuscular junction**, not within the muscle fibers themselves. *Absence of troponin C in muscle fibers* - **Troponin C** is a component of the troponin complex essential for **calcium-mediated muscle contraction**, found inside muscle fibers. - Its absence would lead to severe and widespread muscle dysfunction, unlike the specific and fluctuating weakness seen in **myasthenia gravis**. *Increased transmission at the myoneural junction* - Myasthenia gravis is characterized by **decreased** or **impaired transmission** at the myoneural (neuromuscular) junction due to the destruction or blockade of acetylcholine receptors [2]. - Increased transmission would lead to **muscle hyperactivity** or spasms, which is contrary to the **fatigable weakness** observed in myasthenia gravis.
Question 1095: Anomic aphasia is due to defect in
- A. Left inferior parietal lobe
- B. Left temporal lobe
- C. Temporal occipital lobe (Correct Answer)
- D. Cerebellum
Explanation: ***Temporal occipital lobe*** - Anomic aphasia, characterized by difficulty recalling **words or names (anomia)**, is most commonly associated with lesions in the **left temporo-occipital region**. - This area is crucial for **semantic processing** and word retrieval. *Left inferior parietal lobe* - Damage to the left inferior parietal lobe is more commonly associated with **conduction aphasia**, characterized by impaired repetition despite fluent speech and good comprehension. - It is also involved in aspects of **reading (alexia)** and **writing (agraphia)**. *Left temporal lobe* - While portions of the left temporal lobe (especially Wernicke's area) are critical for language comprehension, damage primarily to this area typically results in **Wernicke's aphasia**, where speech is fluent but meaningless, and comprehension is severely impaired. - Anomia can be a feature of Wernicke's aphasia, but the primary deficit is comprehension. *Cerebellum* - The cerebellum plays a significant role in **motor control**, balance, and coordination, but it is not directly involved in the **generation or comprehension of language** in the same way as cortical areas. - Damage to the cerebellum might lead to **dysarthria** (speech motor difficulties), but not typical aphasia.
Question 1096: What is the preferred test for confirming H. pylori eradication?
- A. Urease breath test (Correct Answer)
- B. Culture
- C. Serological test
- D. Biopsy urease test
Explanation: ***Urease breath test*** - The **urea breath test** is highly sensitive and specific for detecting active *H. pylori* infection and its eradication by measuring radioactive or non-radioactive labeled carbon dioxide released from metabolizing urea. - It is a non-invasive test preferred after treatment to confirm eradication, as it directly detects bacterial urease activity. *Culture* - **Culture** requires an invasive endoscopic biopsy, is expensive, and takes several days to yield results; therefore, it is not the preferred method for routine eradication confirmation. - While it offers the advantage of **antibiotic susceptibility testing**, its invasiveness and turnaround time make it less practical for post-treatment assessment. *Serological test* - **Serological tests** (blood tests for antibodies) remain positive for **H. pylori antibodies** for extended periods even after successful eradication, rendering them unsuitable for confirming eradication. - These tests primarily indicate past exposure rather than current, active infection. *Biopsy urease test* - A **biopsy urease test** involves an invasive endoscopy to obtain a tissue sample, which is then tested for urease activity. - Although useful for initial diagnosis, its invasiveness makes it less preferred for confirming eradication compared to the non-invasive breath test.
Question 1097: Distal renal tubular acidosis is associated with:
- A. Hypocitraturia
- B. Oxalate stones
- C. Calcium stones (Correct Answer)
- D. Uric acid stones
Explanation: ***Calcium stones*** - Distal renal tubular acidosis (Type 1 RTA) causes metabolic acidosis due to impaired distal tubular **hydrogen ion secretion**. - This leads to **increased urinary calcium excretion** (hypercalciuria) and decreased urinary citrate, creating an environment favorable for the formation of **calcium phosphate renal stones**. *Oxalate stones* - While oxalate is a component of some calcium stones (calcium oxalate), **primary hyperoxaluria** or dietary excess of oxalate are the main causes, not directly distal RTA. - Distal RTA specifically promotes **calcium phosphate stone formation** due to pH changes and hypercalciuria. *Hypocitraturia* - **Hypocitraturia** is indeed a feature of distal RTA as the kidney attempts to excrete acid by reabsorbing citrate, making the urine less inhibitory to stone formation. - However, the most direct and common clinically observed consequence in stone formation is the development of **calcium stones**, as hypocitraturia combined with hypercalciuria facilitates their formation. *Uric acid stones* - **Uric acid stones** typically form in persistently **acidic urine** and are associated with conditions like gout or myeloproliferative disorders. - While distal RTA results in systemic acidosis, the urine pH in distal RTA is typically **alkaline or inappropriately neutral**, which does not favor uric acid stone formation.
Ophthalmology
1 questionsWhich structures are most commonly involved in a ciliary staphyloma?
NEET-PG 2012 - Ophthalmology NEET-PG Practice Questions and MCQs
Question 1091: Which structures are most commonly involved in a ciliary staphyloma?
- A. Choroid and sclera
- B. Cornea and conjunctiva
- C. Iris and sclera
- D. Ciliary body and sclera (Correct Answer)
Explanation: ***Ciliary body and sclera*** - A **staphyloma** is a localized bulging of the outer coat of the eye (sclera or cornea) lined internally by uveal tissue. - A **ciliary staphyloma** specifically involves the **ciliary body** and **sclera** at the region of the ciliary body, typically presenting as a dark bluish bulge at the limbal or perilimbal area. - This occurs due to weakening and ectasia of the sclera with prolapse of the underlying ciliary body, commonly seen following scleritis, perforating injuries, or surgeries. *Choroid and sclera* - This combination describes a **posterior staphyloma**, which occurs at the posterior pole of the eye, commonly seen in pathological myopia. - While medically accurate for posterior type, it does not describe a **ciliary staphyloma**. *Iris and sclera* - An **anterior staphyloma** primarily involves bulging of the **cornea** with incarceration of iris tissue, rather than sclera alone. - It occurs after corneal perforation with iris prolapse. *Cornea and conjunctiva* - This does not describe a staphyloma. Bulging of the cornea alone is termed **keratectasia** or **keratoconus**. - The **conjunctiva** is a superficial membrane and is not a structural component of staphyloma formation.
Physiology
2 questionsWhat is the primary mechanism underlying hyperthermia?
Which of the following is used for the diagnosis of asthma?
NEET-PG 2012 - Physiology NEET-PG Practice Questions and MCQs
Question 1091: What is the primary mechanism underlying hyperthermia?
- A. Temperature > 40°C with autonomic dysfunction
- B. Failure of thermoregulation (Correct Answer)
- C. Temperature > 41.5°C
- D. No change in hypothalamic set point
Explanation: ***Failure of thermoregulation*** - **Hyperthermia** is fundamentally caused by the body's inability to dissipate heat effectively, leading to an uncontrolled rise in core body temperature. - This differentiates it from fever, where the **hypothalamic set point** is elevated, and the body actively tries to reach that higher temperature. *Temperature > 41.5°C* - While a temperature exceeding **41.5°C** is often seen in severe hyperthermia, it is a *consequence* of the failure of thermoregulation, not its primary cause. - This extreme temperature indicates a critical state, but the underlying problem is the body's inability to control internal heat. *Temperature > 40°C with autonomic dysfunction* - A temperature above **40°C** combined with **autonomic dysfunction** (e.g., altered mental status, seizures) describes a severe *manifestation* of hyperthermia, often seen in heat stroke. - This is a symptom complex resulting from, rather than the primary cause of, the body's thermoregulatory failure. *No change in hypothalamic set point* - This statement is a *characteristic* of hyperthermia, distinguishing it from fever, where the **hypothalamic set point** is elevated. - However, the *absence* of this change is not the primary cause; rather, the underlying issue is the body's inability to manage its heat load despite a normal set point.
Question 1092: Which of the following is used for the diagnosis of asthma?
- A. Measurement of tidal volume
- B. End expiratory flow rate
- C. Total lung capacity
- D. FEV1 (Correct Answer)
Explanation: ***FEV1*** - **Forced expiratory volume in 1 second (FEV1)** is the gold standard spirometric parameter for asthma diagnosis - Key diagnostic criteria include: - Reduced **FEV1/FVC ratio** (<0.70 or <0.75-0.80 in adults) - **Bronchodilator reversibility**: ≥12% and ≥200 mL increase in FEV1 after inhaled short-acting β2-agonist - This reversibility distinguishes asthma from fixed obstructive diseases like COPD - Serial **peak expiratory flow (PEF)** monitoring can also demonstrate variability characteristic of asthma *Measurement of tidal volume* - **Tidal volume** measures the amount of air inhaled or exhaled during normal breathing (typically ~500 mL at rest) - Not a diagnostic parameter for asthma as it doesn't assess **airway obstruction** or **hyperresponsiveness** - May be reduced during acute exacerbations but lacks specificity for asthma diagnosis *End expiratory flow rate* - Not a standard diagnostic parameter for asthma - While **mid-expiratory flow rates** (FEF25-75%) and **peak expiratory flow (PEF)** are assessed, **FEV1** remains the primary diagnostic measure - FEV1 provides better reproducibility and standardization for diagnosis *Total lung capacity* - **Total lung capacity (TLC)** represents total lung volume after maximal inhalation - May be normal or increased in asthma due to **air trapping** and hyperinflation - Not used as a primary diagnostic criterion as asthma diagnosis focuses on demonstrating **reversible airflow limitation**, not lung volumes