Internal Medicine
1 questionsWhat will the aspirated synovial fluid in a case of septic arthritis typically show?
NEET-PG 2013 - Internal Medicine NEET-PG Practice Questions and MCQs
Question 1371: What will the aspirated synovial fluid in a case of septic arthritis typically show?
- A. Clear and straw-colored fluid
- B. Low viscosity fluid
- C. Cloudy or purulent fluid
- D. Markedly increased polymorphonuclear leukocytes (Correct Answer)
Explanation: ***Markedly increased polymorphonuclear leukocytes*** - **Septic arthritis** is characterized by an acute infection within the joint, leading to a profound inflammatory response with a significant influx of **neutrophils** (polymorphonuclear leukocytes) into the synovial fluid. - A synovial leukocyte count greater than **50,000 cells/mm³** with over **75% neutrophils** is highly suggestive of septic arthritis. *Clear and straw-colored fluid* - This description typically corresponds to **normal synovial fluid** or fluid from a mild **non-inflammatory condition**, which is not consistent with bacterial infection. - Normal synovial fluid is usually **transparent**, indicating the absence of significant cellular debris or inflammatory cells. *Low viscosity fluid* - While septic synovial fluid can have reduced viscosity due to the breakdown of **hyaluronic acid** by bacterial enzymes and inflammatory mediators, this characteristic alone is not the most definitive diagnostic feature. - Reduced viscosity is also observed in other inflammatory conditions, making it less specific than direct cellular analysis for diagnosing infection. *Cloudy or purulent fluid* - The presence of **cloudy** or **purulent (pus-like)** fluid *is* often seen in septic arthritis, reflecting the high cell count and protein content. - However, this is a **gross visual observation**, and a more precise and diagnostic indicator is the microscopic finding of markedly increased **polymorphonuclear leukocytes**.
Orthopaedics
3 questionsHow is Brodie's abscess classified?
Thurston Holland sign is seen in ?
Which of the following is NOT a common fracture in children?
NEET-PG 2013 - Orthopaedics NEET-PG Practice Questions and MCQs
Question 1371: How is Brodie's abscess classified?
- A. Acute osteomyelitis
- B. Subacute osteomyelitis
- C. Septic arthritis
- D. Chronic osteomyelitis (Brodie's abscess) (Correct Answer)
Explanation: ***Chronic osteomyelitis (Brodie's abscess)*** - Brodie's abscess is a **subacute or chronic localized osteomyelitis**, characterized by an intraosseous abscess often surrounded by a thick layer of sclerotic bone. - It represents a **contained infection** within the bone, lacking the widespread inflammatory response seen in acute forms. *Acute osteomyelitis* - Characterized by a **rapid onset** of severe pain, fever, and inflammation, usually within days to weeks of infection. - It involves a **widespread inflammatory process** and potential for bone destruction, differentiated from the contained and indolent nature of Brodie's abscess. *Subacute osteomyelitis* - This term describes an osteomyelitis with a more gradual onset and less severe symptoms than acute osteomyelitis, typically lasting several weeks to a few months. - While Brodie's abscess can present subacutely, it is specifically classified as a **form of chronic osteomyelitis** due to its localized, walled-off nature and prolonged course. *Septic arthritis* - Involves an infection within a **joint space**, leading to inflammation and destruction of articular cartilage. - It is distinct from Brodie's abscess, which is an infection of the **bone tissue itself**, not the joint.
Question 1372: Thurston Holland sign is seen in ?
- A. Type II (Correct Answer)
- B. Type I
- C. Type III
- D. Type IV
Explanation: ***Type II*** - The **Thurston Holland sign** is characteristic of a **Salter-Harris Type II fracture**, often described as a metaphyseal fragment (the "Thurston Holland fragment") remaining attached to the epiphyseal plate. - This fragment typically occurs at the corner of the **metaphysis**, making the fracture line extend obliquely through the physis and then along the metaphysis. *Type I* - A **Salter-Harris Type I fracture** involves a clean horizontal separation through the **growth plate (physis)** without involving the metaphysis or epiphysis. - No metaphyseal fragment is seen in Type I fractures, distinguishing it from the Thurston Holland sign. *Type III* - **Salter-Harris Type III fractures** extend from the **physis into the epiphysis**, creating an intra-articular fracture involving the joint surface. - These fractures do not involve a metaphyseal fragment, as they solely affect the physis and epiphysis. *Type IV* - **Salter-Harris Type IV fractures** involve a fracture line extending through the **epiphysis, physis, and metaphysis**, effectively dividing the bone into three parts. - While complex, Type IV injuries do not specifically describe the characteristic metaphyseal fragment that defines the Thurston Holland sign.
Question 1373: Which of the following is NOT a common fracture in children?
- A. Supracondylar humerus
- B. Fracture of hand (Correct Answer)
- C. Radius-ulna fracture
- D. Lateral condyle humerus
Explanation: ***Fracture of hand*** - While hand fractures can occur in children, they are generally **less common** compared to fractures of the long bones, especially those of the **upper extremity**, due to the types of activities and falls children typically experience. - The small bones of the hand are often better protected or less frequently exposed to severe direct trauma in routine childhood activities that lead to fractures elsewhere. *Lateral condyle humerus* - This is a common and often challenging fracture in children, particularly affecting those aged 6-10 years. - It usually results from a fall on an **outstretched hand**, with the elbow in extension. *Supracondylar humerus* - This is one of the **most common elbow fractures** in children and is typically due to a fall on an **outstretched hand** with the elbow extended or hyperextended. - Its significance lies in the potential for neurovascular complications due to its proximity to vital structures. *Radius-ulna fracture* - **Forearm fractures** involving the radius, ulna, or both are extremely common in children, often resulting from falls onto an **outstretched hand**. - The **distal radius** is a particularly frequent site of fracture in this age group.
Pathology
2 questionsWhich of the following statements about chronic osteomyelitis is false?
All are features of Paget's disease except which of the following?
NEET-PG 2013 - Pathology NEET-PG Practice Questions and MCQs
Question 1371: Which of the following statements about chronic osteomyelitis is false?
- A. Reactive new bone formation
- B. Cloaca is an opening in involucrum
- C. Involucrum is dead bone (Correct Answer)
- D. Sequestrum is hard and dense
Explanation: ***Involucrum is dead bone*** - This statement is false because the **involucrum** is the layer of **new bone formation** that surrounds a segment of necrotic (dead) bone, known as the **sequestrum**, in chronic osteomyelitis [1]. - The involucrum represents the body's attempt to wall off the infection and dead bone, and thus, it is living, *reactive bone*, not dead bone [1]. *Reactive new bone formation* - This statement is true; **reactive new bone formation** occurs around infected or necrotic bone in chronic osteomyelitis, forming the **involucrum** [1]. - This process is a hallmark of the body's response to chronic infection and attempts to contain it. *Cloaca is an opening in involucrum* - This statement is true; a **cloaca** is a **fistulous tract** or opening in the **involucrum** that allows pus and necrotic debris from the infected area to drain to the skin surface. - This drainage is a common clinical sign of chronic osteomyelitis. *Sequestrum is hard and dense* - This statement is true; the **sequestrum** is a piece of **necrotic (dead) bone** that has become separated from living bone due to ischemia and infection [1]. - Due to the loss of blood supply and avascular necrosis, it appears **dense, hard, and radiodense** on imaging, representing devitalized bone tissue that is walled off from the body's immune response. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Bones, Joints, and Soft Tissue Tumors, pp. 1197-1198.
Question 1372: All are features of Paget's disease except which of the following?
- A. Defect in osteoclasts
- B. Affects only axial skeleton (Correct Answer)
- C. Can lead to hearing loss
- D. Can lead to bone cancer
Explanation: ***Affects only axial skeleton*** - This statement is **FALSE** and therefore the correct answer to this "EXCEPT" question. - Paget's disease **can affect any bone in the body**, including both axial skeleton (spine, skull, pelvis) and appendicular skeleton (femur, tibia, humerus) [1]. - Common sites include: **pelvis (70%), spine, skull, femur, and tibia** [1]. - While it frequently affects axial bones, it is **not exclusive** to them. *Defect in osteoclasts* - This is a TRUE feature of Paget's disease. - The disease is characterized by **abnormal, hyperactive osteoclasts** with increased number of nuclei (up to 100 vs normal 3-5). - These osteoclasts show **excessive bone resorption activity** followed by disorganized bone formation [1]. - The primary defect involves **increased osteoclast activity and sensitivity to RANKL**. *Can lead to hearing loss* - This is a TRUE feature of Paget's disease. - Skull involvement can lead to **compression of cranial nerve VIII** (vestibulocochlear nerve) [1]. - Enlargement and disorganization of temporal bone can cause **conductive or sensorineural hearing loss**. - Occurs in approximately 30-50% of patients with skull involvement. *Can lead to bone cancer* - This is a TRUE feature of Paget's disease. - **Osteosarcoma** develops in approximately **1%** of Paget's disease patients. - Risk is higher in patients with **polyostotic disease** and long-standing involvement. - This is a rare but serious complication with poor prognosis. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Bones, Joints, and Soft Tissue Tumors, pp. 1192-1194.
Radiology
3 questionsWhat is the maximum radiation dose (in Gray) that bone tissue can tolerate?
Which condition is characterized by a 'moth-eaten' appearance of the bones?
In which condition is the 'Picture frame vertebra' seen?
NEET-PG 2013 - Radiology NEET-PG Practice Questions and MCQs
Question 1371: What is the maximum radiation dose (in Gray) that bone tissue can tolerate?
- A. 50 Gray (Correct Answer)
- B. 30 Gray
- C. 20 Gray
- D. 40 Gray
Explanation: ***Correct Option: 50 Gray*** - The **maximum radiation tolerance dose** for bone tissue is approximately **50-60 Gray (Gy)** based on radiobiology literature and clinical practice. - Among the given options, **50 Gy** represents the most appropriate threshold for bone tolerance. - According to **Emami et al. tolerance doses** and **QUANTEC guidelines**, bone can typically tolerate up to 60 Gy without significant risk of complications. - Doses approaching or exceeding **60 Gy** carry increased risk of **osteoradionecrosis**, particularly in the **mandible and weight-bearing bones**. - **Clinical significance**: In radiation therapy planning, doses of 50-60 Gy to bone are commonly used therapeutically for tumors involving or adjacent to bone. *Incorrect Option: 40 Gray* - 40 Gy is **below the accepted tolerance threshold** for bone tissue. - This dose is generally **well-tolerated** by bone without significant risk of necrosis or fracture. - Commonly used in palliative and definitive radiation protocols without major bone complications. *Incorrect Option: 30 Gray* - 30 Gy is **considerably below** the tolerance limit for bone. - This dose level is **safe for bone tissue** and carries minimal risk of radiation-induced bone damage. - Often used in palliative treatments with excellent bone tolerance. *Incorrect Option: 20 Gray* - 20 Gy is a **low radiation dose** from the perspective of bone tolerance. - This dose is **highly unlikely** to cause any significant bone damage or complications. - Represents a conservative therapeutic dose well within safety margins.
Question 1372: Which condition is characterized by a 'moth-eaten' appearance of the bones?
- A. Osteoid osteoma
- B. Multiple myeloma (Correct Answer)
- C. Eosinophilic granuloma
- D. Chondromyxoid fibroma
Explanation: ***Multiple myeloma*** [1][2] - Characterized by **punched-out lytic lesions** in bones, often described as **moth-eaten** appearance on imaging [1]. - Associated with **elevated serum proteins** and **Bence Jones proteins** in urine, confirming the diagnosis [2]. *Eosinophilic granuloma* - Usually presents with **solitary bone lesions** and is linked to **Langerhans cell histiocytosis** rather than the moth-eaten pattern. - Does not typically cause generalized **lytic bone lesions** seen in cases of multiple myeloma. *Chondromyxoid fibroma* - Generally appears as a **well-defined cortical lesion** and is not associated with a moth-eaten appearance. - It predominantly affects the **metaphysis** of long bones and shows a characteristic **cartilaginous matrix**. *Osteoid osteoma* - Presents with a **nidus** of osteoid formation, leading to localized bone pain, and does not exhibit a moth-eaten consistency. - Tends to cause **cortical bone thickening** rather than the diffuse lytic lesions associated with multiple myeloma. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, p. 608. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 616-617.
Question 1373: In which condition is the 'Picture frame vertebra' seen?
- A. Paget disease (Correct Answer)
- B. Osteopetrosis (marble bone disease)
- C. Ankylosing spondylitis (AS)
- D. Osteoporosis
Explanation: ***Paget disease*** - The "picture frame vertebra" sign is a classic radiographic finding in **Paget disease**, characterized by **cortical thickening** and sclerosis around the vertebral body circumference, resembling a picture frame. - This appearance is due to the disordered bone remodeling processes (increased osteoclastic bone resorption followed by disorganized osteoblastic new bone formation) characteristic of Paget disease. *Osteopetrosis (marble bone disease)* - Osteopetrosis is characterized by **increased bone density** due to defective osteoclast function, leading to bones that are dense but brittle. - It does not typically present with the specific "picture frame" appearance of individual vertebrae, but rather with diffuse sclerosis of bones. *Ankylosing spondylitis (AS)* - Ankylosing spondylitis primarily affects the **axial skeleton**, causing inflammation and eventual fusion of the vertebrae (leading to a "bamboo spine" appearance). - While it involves the spine, it does not produce the "picture frame" vertebral sign seen in Paget disease. *Osteoporosis* - Osteoporosis is characterized by **reduced bone mass** and microstructural deterioration of bone tissue, leading to increased bone fragility and fracture risk. - Radiographically, it shows **decreased bone density** and possible vertebral compression fractures, which is the opposite of the increased bone density and cortical thickening seen in the "picture frame" sign.
Surgery
1 questionsWhat is considered a poor prognostic indicator in Pott's paraplegia?
NEET-PG 2013 - Surgery NEET-PG Practice Questions and MCQs
Question 1371: What is considered a poor prognostic indicator in Pott's paraplegia?
- A. Healed disease
- B. Chronic disease
- C. Rapid progression of neurological deficits (Correct Answer)
- D. Active disease
Explanation: ***Rapid progression of neurological deficits*** - **Rapid progression** implies severe spinal cord damage occurring quickly, which is less likely to fully recover even with treatment. - This indicates a more aggressive disease process or significant compression that can lead to irreversible neurological impairment. *Healed disease* - **Healed disease** (even if paraplegia existed previously) indicates that the infection is resolved and the destructive process has stopped, allowing for potential neurological recovery or stability. - While residual neurological deficits might remain, the absence of active inflammation improves the long-term prognosis compared to ongoing damage. *Chronic disease* - **Chronic disease** in the context of Pott's paraplegia often refers to established deficits after a prolonged course, but it doesn't necessarily imply ongoing active deterioration. - The chronicity itself, without rapid progression, suggests a more stable state where the damage has already occurred, and further deterioration might be slow or absent. *Active disease* - **Active disease** means the infection is still present and causing bone destruction, which is a concern. - However, if the neurological deficits are not rapidly progressing, there is still a window for treatment to stop the disease and potentially allow for some recovery, distinguishing it from an acute, rapidly deteriorating situation.