Neuroradiology Practice Questions

Q: Intracranial calcification is characteristic of which of the following conditions?

Sturge-Weber syndrome. **Explanation:** **Sturge-Weber Syndrome (SWS)**, also known as encephalotrigeminal angiomatosis, is a neurocutaneous disorder characterized by a facial port-wine stain, glaucoma, and leptomeningeal angiomas. The hallmark radiological finding in SWS is **intracranial calcification**. This occurs due to chronic hypoxia and venous stasis underlying the leptomeningeal angioma, leading to cortical atrophy and "tram-track" or "railroad track" calcifications (gyriform calcifications) typically seen on CT scans in the parietal and occipital lobes. **Analysis of Incorrect Options:** * **Stevens-Johnson Syndrome (B):** A severe mucocutaneous hypersensitivity reaction, usually drug-induced. It involves extensive epidermal necrolysis but does not cause intracranial calcifications. * **Papillon-Lefèvre Syndrome (C):** An autosomal recessive disorder characterized by palmoplantar keratoderma and early-onset periodontitis. It is associated with dural calcifications (e.g., falx cerebri), but not the characteristic parenchymal intracranial calcifications seen in neurocutaneous syndromes. * **Hallermann-Streiff Syndrome (D):** A rare genetic disorder involving craniofacial abnormalities (bird-like facies), cataracts, and hypotrichosis. It does not feature intracranial calcifications. **High-Yield Clinical Pearls for NEET-PG:** * **Imaging Gold Standard:** CT is the most sensitive modality to detect the "tram-track" calcifications. * **MRI Findings:** Shows "pial enhancement" due to the leptomeningeal angioma and enlarged ipsilateral choroid plexus. * **Clinical Triad:** Facial port-wine stain (Trigeminal nerve distribution, V1/V2), seizures, and glaucoma. * **Other Calcifications:** Remember **Tuberous Sclerosis** (Subependymal nodules/tubers) and **Fahr’s Disease** (Basal ganglia calcification) as common differentials for intracranial calcifications.

Q: What is the best radiographic view for a fracture of the C1-C2 vertebrae?

Odontoid view. The **Odontoid view** (also known as the **Open-mouth view**) is the gold standard radiographic projection for evaluating the C1 (Atlas) and C2 (Axis) vertebrae. ### Why the Odontoid View is Correct The upper cervical spine is normally obscured in a standard AP view by the overlying mandible and the base of the skull. By opening the mouth wide, these structures are displaced, allowing a clear view of the **dens (odontoid process)**, the **atlanto-axial joints**, and the **lateral masses of C1**. This view is essential for diagnosing: * **Jefferson fractures** (burst fracture of C1): Indicated by lateral displacement of the C1 lateral masses. * **Odontoid fractures**: Visualizing fractures through the dens. ### Why Other Options are Incorrect * **AP View:** The mandible and occiput superimpose over the upper cervical vertebrae, making C1 and C2 invisible or poorly defined. * **Lateral View:** While excellent for seeing the "Pre-vertebral space" and the "Atlantodental interval (ADI)," it cannot visualize the lateral masses or the symmetry of the atlanto-axial joint. * **Oblique View:** Primarily used to visualize the **neural foramina** and facet joints of the lower cervical spine (C3-C7), not the C1-C2 complex. ### Clinical Pearls for NEET-PG * **Rule of Spence:** On an odontoid view, if the combined lateral displacement of C1 lateral masses over C2 is **>6.9 mm**, it indicates a rupture of the **Transverse Axial Ligament**. * **Harris Ring:** A radiopaque ring seen on the **Lateral view** of C2; a break in this ring suggests a Hangman’s fracture. * **Gold Standard Imaging:** While the Odontoid view is the best *radiographic* view, **Non-contrast CT (NCCT)** is the overall gold standard for diagnosing cervical spine fractures in trauma.

Q: J-shaped sella is/are seen in which of the following conditions?

All of the above. ### Explanation The **J-shaped sella** (also known as the **omega sella**) is a classic radiological sign seen on a lateral skull X-ray or sagittal MRI. It is characterized by an elongated, flattened sella turcica with a shallow anterior notch, resembling the letter ‘J’ or the Greek letter ‘$\Omega$’. #### Why "All of the Above" is Correct: The J-shaped sella occurs due to the erosion or remodeling of the **tuberculum sellae** and the **chiasmatic sulcus**. The conditions listed cause this through different mechanisms: 1. **Optic Chiasm Glioma (Option C):** This is the most common cause. The tumor grows near the optic chiasm, causing pressure erosion of the anterior aspect of the sella turcica, leading to its characteristic elongation. 2. **Mucopolysaccharidoses (Option A):** Specifically Hurler syndrome (MPS I) and Hunter syndrome (MPS II). Dysostosis multiplex leads to defective bone formation and deposition of glycosaminoglycans, resulting in a wide, shallow sella. 3. **Achondroplasia (Option B):** In this condition, the skull base is shortened due to premature synchondrosis, which alters the morphology of the sella turcica into a J-shape. #### High-Yield Clinical Pearls for NEET-PG: * **Normal Sella:** Usually has a "cup-shaped" appearance. * **Empty Sella Syndrome:** Characterized by an enlarged sella filled with CSF, with a flattened pituitary gland. * **Ballooned Sella:** Typically seen in **Pituitary Adenomas**, where the sella expands in all directions. * **Other causes of J-shaped sella:** Chronic compensated hydrocephalus and neurofibromatosis type 1 (NF1). * **Key Distinction:** While "J-shaped sella" is often associated with optic gliomas in pediatric exams, always look for "All of the above" if MPS or Achondroplasia are listed.

Q: What is the investigation of choice for temporal bone injury?

CT scan. **Explanation:** The temporal bone is a complex anatomical structure containing the auditory and vestibular apparatus. For any suspected temporal bone injury (trauma), **High-Resolution Computed Tomography (HRCT)** is the investigation of choice. **1. Why CT scan is the Correct Answer:** CT provides superior spatial resolution for visualizing cortical bone and delicate intratemporal structures. It is the gold standard for identifying: * **Fracture lines:** Differentiating between longitudinal (more common) and transverse (higher risk of facial nerve palsy) fractures. * **Ossicular chain integrity:** Detecting dislocations (e.g., incudostapedial joint) or fractures. * **Pneumocranium/CSF otorrhea:** Identifying bony defects in the tegmen tympani or tegmen mastoideum. **2. Why other options are incorrect:** * **MRI:** While excellent for soft tissues (e.g., evaluating the facial nerve or membranous labyrinth), it cannot visualize bony architecture or fracture lines clearly. * **Angiography:** Reserved only if vascular injury (e.g., internal carotid artery dissection or sigmoid sinus thrombosis) is suspected following the initial CT. * **Plain X-ray:** Obsolete in modern trauma management due to the overlapping of complex cranial structures, which leads to very low sensitivity. **High-Yield Clinical Pearls for NEET-PG:** * **Longitudinal Fractures:** Most common (80%); usually caused by lateral blows; often associated with conductive hearing loss. * **Transverse Fractures:** Less common (20%); caused by frontal/occipital blows; higher risk of **sensorineural hearing loss** and **facial nerve injury**. * **Iceberg Sign:** On CT, a soft tissue density in the middle ear (hemotympanum) may be the only sign of an underlying fracture.

Q: A 40-year-old man presented to the emergency room with loss of consciousness following a high-energy motor vehicle collision. He is a known alcoholic and hypertensive. His non-contrast CT head showed no lesion explaining the coma, and his GCS is 8. An urgent MRI was performed. What is the most likely diagnosis?

Diffuse axonal injury. ***Diffuse axonal injury*** - **CT showing no lesion explaining the coma** with severe neurological deficit (**GCS 8**) suggests microscopic injury requiring **MRI** for detection, characteristic of diffuse axonal injury. Accompanying hemorrhagic contusions may also be present on MRI. - **MRI sequences** like **SWI/GRE** show **microhemorrhages** at **grey-white junction** and **corpus callosum**, pathognomonic for DAI; these susceptibility foci at characteristic locations support diffuse axonal injury only in the appropriate traumatic context, such as a high-energy acceleration-deceleration mechanism. *Cerebral amyloid angiopathy* - Typically affects **elderly patients over 65 years** with recurrent **lobar hemorrhages**, not a 40-year-old. - Characterized by **cortical-subcortical hemorrhages** in specific lobar distributions, not diffuse microscopic injury. *Subarachnoid hemorrhage* - Would be **visible on non-contrast CT** in acute phase (within 24-48 hours) as **hyperdense blood** in subarachnoid spaces. - Associated with **severe headache**, **neck stiffness**, and **photophobia**, not isolated loss of consciousness with normal CT. *Subdural hematoma* - Appears as **hyperdense crescent-shaped lesion** on **CT scan**, easily visible and would not require MRI for diagnosis. - More common in **elderly patients** or those with **brain atrophy**, presenting with **focal neurological deficits** rather than diffuse injury pattern.

Q: Which condition is characterized by 'tram-track calcification' in the brain?

Sturge-Weber syndrome. **Explanation:** **Sturge-Weber Syndrome (SWS)**, also known as encephalotrigeminal angiomatosis, is the correct answer. The characteristic **'tram-track' calcification** (also called railroad track sign) refers to curvilinear, parallel lines of calcification seen on a CT scan or skull X-ray. This occurs due to calcification of the underlying atrophic cortical gray matter (specifically layers II and III) beneath a leptomeningeal venous angioma. It typically involves the occipital and parietal lobes. **Analysis of Incorrect Options:** * **Toxoplasmosis:** Characterized by **scattered, nodular intracranial calcifications** (usually in the basal ganglia and corticomedullary junction) rather than linear cortical patterns. * **Tuberous Sclerosis:** Features **subependymal nodules** (candle-guttering appearance) and cortical hamartomas (tubers) which may calcify, but they do not form a tram-track pattern. * **Syphilis:** Neurosyphilis may present with "gummas" or vasculitis, but it is not typically associated with specific patterns of intracranial calcification. **High-Yield Clinical Pearls for NEET-PG:** * **SWS Triad:** 1. Port-wine stain (Nevus flammeus) in the V1/V2 distribution of the trigeminal nerve; 2. Leptomeningeal angioma (ipsilateral); 3. Glaucoma. * **Imaging Gold Standard:** **Contrast-enhanced MRI** is the most sensitive modality to detect leptomeningeal enhancement (pial angiomatosis) early in life, before calcifications develop. * **GNAQ Gene:** SWS is caused by a somatic mutation in the *GNAQ* gene; it is sporadic and not inherited. * **Clinical Presentation:** Often presents with refractory seizures, hemiparesis, and intellectual disability.

Q: A patient presented with contralateral hemiplegia and sub-periosteal bleeding. What is the initial investigation of choice?

CT scan. **Explanation:** The clinical presentation of **contralateral hemiplegia** (weakness on one side of the body) combined with **sub-periosteal bleeding** (often referring to a cephalhematoma or traumatic skull injury in this context) strongly suggests an **acute intracranial hemorrhage** or a traumatic brain injury (TBI). **1. Why CT Scan is the Correct Answer:** Non-Contrast Computed Tomography (NCCT) of the head is the **initial investigation of choice** in acute neurological emergencies. * **Speed:** It is rapid, making it ideal for unstable patients. * **Sensitivity:** It is highly sensitive (nearly 100%) for detecting **acute blood** (which appears hyperdense/white). * **Bone Pathology:** It is superior to MRI for identifying associated skull fractures or sub-periosteal involvement. * **Availability:** It is widely available in emergency departments. **2. Why Other Options are Incorrect:** * **Chest X-ray:** While useful for systemic trauma assessment, it provides no information regarding intracranial pathology or hemiplegia. * **MRI:** Although more sensitive for diffuse axonal injury or posterior fossa strokes, it is time-consuming, expensive, and difficult to perform on unstable patients. It is generally the "investigation of choice" for chronic conditions or subacute infarcts, but not the *initial* step in acute trauma/hemorrhage. * **PET Scan:** This is a functional imaging modality used primarily in oncology and dementia workups; it has no role in the acute management of hemiplegia. **Clinical Pearls for NEET-PG:** * **Acute Blood on CT:** Appears **Hyperdense** (White). * **Chronic Blood on CT:** Appears **Hypodense** (Black). * **Epidural Hematoma (EDH):** Biconvex/Lens-shaped; does not cross sutures. * **Subdural Hematoma (SDH):** Crescent-shaped; can cross sutures. * **Gold Standard for Stroke:** NCCT Head is the first step to rule out hemorrhage before starting thrombolysis.

Q: A male was brought unconscious to the hospital with external injuries. CT brain showed no midline shift, but basal cisterns were compressed with multiple small hemorrhages. What is the diagnosis?

Diffuse axonal injuries. **Explanation:** The clinical presentation of an unconscious patient with a high-impact head injury, where CT findings show minimal mass effect (no midline shift) but significant signs of increased intracranial pressure (compressed basal cisterns) and punctate hemorrhages, is classic for **Diffuse Axonal Injury (DAI)**. **Why D is Correct:** DAI occurs due to sudden rotational acceleration/deceleration forces causing shearing of axons. The hallmark of DAI on imaging is **multiple small, petechial hemorrhages** located at specific interfaces: the grey-white matter junction (most common), corpus callosum, and brainstem. A key diagnostic clue is the **clinicoradiological dissociation**: the patient’s clinical state (comatose/GCS <8) is much worse than what the initial CT scan suggests. **Why Incorrect Options are Wrong:** * **A & B (Cortical Contusion/Laceration):** These are focal injuries typically found at the site of impact (coup) or opposite to it (contrecoup), usually involving the frontal and temporal poles. They present as larger, localized areas of edema and hemorrhage, often causing a midline shift. * **C (Multiple Infarcts):** These typically follow a vascular territory or "watershed" distribution and are usually seen in embolic events or severe hypoxia, not acutely following trauma with external injuries. **High-Yield Clinical Pearls for NEET-PG:** * **Gold Standard Investigation:** **MRI (specifically Susceptibility Weighted Imaging - SWI)** is the most sensitive sequence for detecting the microhemorrhages of DAI that CT might miss. * **Grading (Adams Classification):** * **Grade I:** Grey-white matter junction. * **Grade II:** Corpus callosum (Splenium). * **Grade III:** Brainstem (Dorsolateral aspect). * **Key Phrase:** Look for "Clinicoradiological dissociation" or "Normal CT in a comatose patient" to suspect DAI.

Q: A 45-year-old man with AIDS presents with misperceptions, tiredness, and memory loss. Which imaging feature favors a diagnosis of progressive multifocal leukoencephalopathy over HIV encephalopathy?

Bilateral asymmetrical peripheral subcortical lesions. ### Explanation The clinical presentation of cognitive decline in an AIDS patient necessitates a distinction between **Progressive Multifocal Leukoencephalopathy (PML)** and **HIV Encephalopathy (HIVE)**. **Why Option D is Correct:** PML is caused by the reactivation of the **JC virus**, which infects oligodendrocytes. On MRI, it typically presents as **bilateral, asymmetrical** white matter hyperintensities on T2/FLAIR. A hallmark feature of PML is its predilection for the **peripheral subcortical white matter**, specifically involving the **subcortical U-fibers**, giving the lesions a "scalloped" appearance at the gray-white matter junction. **Why Other Options are Incorrect:** * **A & B (Mass effect and Contrast enhancement):** Both PML and HIVE are typically **non-enhancing** and do **not** exhibit mass effect. The presence of enhancement or mass effect should prompt consideration of CNS Lymphoma or Toxoplasmosis. * **C (Bilateral symmetrical periventricular lesions):** This is the classic description of **HIV Encephalopathy**. HIVE tends to be diffuse, symmetric, and characteristically **spares the subcortical U-fibers**, localized instead in the deep periventricular white matter. **NEET-PG High-Yield Pearls:** 1. **PML:** Asymmetric + Peripheral (U-fibers involved) + Scalloped borders. 2. **HIVE:** Symmetric + Central/Periventricular (U-fibers spared) + Associated with diffuse cerebral atrophy. 3. **Imaging Modality of Choice:** MRI is far more sensitive than CT for both conditions. 4. **CD4 Count:** PML usually occurs when CD4 < 100 cells/µL, whereas HIVE can occur at slightly higher levels but is most severe in advanced AIDS.

Q: What condition is associated with the "Radial Band" sign on MRI Brain?

Tuberous sclerosis. ### Explanation **Correct Answer: B. Tuberous Sclerosis** The **"Radial Band" sign** is a highly specific neuroimaging feature of **Tuberous Sclerosis Complex (TSC)**. These bands represent linear or curvilinear areas of abnormal signal intensity extending from the periventricular white matter to the subcortical region (cortex). * **Pathophysiology:** They correspond to **migratory tracks** of dysplastic glial cells and neurons that failed to reach the cortical surface during embryogenesis. * **MRI Appearance:** They are best visualized on **FLAIR** or **T2-weighted** sequences as hyperintense lines following the path of the radial glial fibers. --- ### Why the other options are incorrect: * **A. Multiple Sclerosis:** Characterized by **Dawson’s Fingers**, which are ovoid demyelinating plaques oriented perpendicular to the lateral ventricles, representing perivenular inflammation. * **C. Multisystem Atrophy type C (MSA-C):** Classically associated with the **"Hot Cross Bun" sign**, representing degeneration of the pontine fibers and raphe nuclei. * **D. Progressive Supranuclear Palsy (PSP):** Associated with the **"Hummingbird" sign** or **"Mickey Mouse" sign** due to midbrain atrophy with preservation of the pons. --- ### High-Yield Clinical Pearls for NEET-PG: 1. **Vogt’s Triad (TSC):** Adenoma sebaceum (facial angiofibromas), Mental retardation, and Seizures (only seen in ~30% of patients). 2. **Other CNS findings in TSC:** * **Cortical Tubers:** Hamartomatous lesions (90% of cases). * **Subependymal Nodules (SEN):** Located along the walls of lateral ventricles; often calcified ("Candle guttering"). * **SEGA (Subependymal Giant Cell Astrocytoma):** A benign tumor typically located near the Foramen of Monro, which can cause obstructive hydrocephalus. 3. **Ash-leaf spots:** Often the earliest clinical sign of TSC, visible under Wood’s lamp.

Question 1

Intracranial calcification is characteristic of which of the following conditions?

Accepted Answer

Sturge-Weber syndrome

Answer

Stevens-Johnson syndrome

Answer

Papillon-Lefèvre syndrome

Answer

Hallermann-Streiff syndrome

Question 2

What is the best radiographic view for a fracture of the C1-C2 vertebrae?

Accepted Answer

Odontoid view

Answer

AP view

Answer

Lateral view

Answer

Oblique view

Question 3

J-shaped sella is/are seen in which of the following conditions?

Accepted Answer

All of the above

Answer

Mucopolysaccharidoses

Answer

Achondroplasia

Answer

Optic chiasm glioma

Question 4

What is the investigation of choice for temporal bone injury?

Accepted Answer

CT scan

Answer

MRI

Answer

Angiography

Answer

Plain x-ray

Question 5

A 40-year-old man presented to the emergency room with loss of consciousness following a high-energy motor vehicle collision. He is a known alcoholic and hypertensive. His non-contrast CT head showed no lesion explaining the coma, and his GCS is 8. An urgent MRI was performed. What is the most likely diagnosis?

Accepted Answer

Diffuse axonal injury

Answer

Subarachnoid hemorrhage

Answer

Cerebral amyloid angiopathy

Answer

Subdural hematoma

Question 6

Which condition is characterized by 'tram-track calcification' in the brain?

Accepted Answer

Sturge-Weber syndrome

Answer

Toxoplasmosis

Answer

Tuberous sclerosis

Answer

Syphilis

Question 7

A patient presented with contralateral hemiplegia and sub-periosteal bleeding. What is the initial investigation of choice?

Accepted Answer

CT scan

Answer

Chest x-ray

Answer

MRI

Answer

PET scan

Question 8

A male was brought unconscious to the hospital with external injuries. CT brain showed no midline shift, but basal cisterns were compressed with multiple small hemorrhages. What is the diagnosis?

Accepted Answer

Diffuse axonal injuries

Answer

Cortical contusion

Answer

Cerebral laceration

Answer

Multiple infarcts

Question 9

A 45-year-old man with AIDS presents with misperceptions, tiredness, and memory loss. Which imaging feature favors a diagnosis of progressive multifocal leukoencephalopathy over HIV encephalopathy?

Accepted Answer

Bilateral asymmetrical peripheral subcortical lesions

Answer

Mass effect present

Answer

Contrast enhancement

Answer

Bilateral symmetrical periventricular lesions

Question 10

What condition is associated with the "Radial Band" sign on MRI Brain?

Accepted Answer

Tuberous sclerosis

Answer

Multiple sclerosis

Answer

Multisystem atrophy type C

Answer

Progressive supranuclear palsy

Neuroradiology — MCQs

Neuroradiology — MCQs

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