LE 1 NEURO 2024 Flashcards

1
Q

Which of the following terms describes a person who wakes up and then goes back to sleep?

A. Lethargic
B. Alert
C. Obtunded
D. Stupor

A

A. Lethargic

Rationale:
According to Harrison’s Principles of Internal Medicine, lethargy is a state in which a person is drowsy but can be aroused to full wakefulness, though they may return to sleep when left undisturbed. This differentiates it from stupor or obtundation, where arousal to full wakefulness is more challenging and often requires persistent stimuli.

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2
Q

Which of the following is not a characteristic of uncal herniation?

A. Large non-reactive pupil
B. Respiratory arrest
C. Decreased sensorium
D. Intractable seizure

A

D. Intractable seizure

Rationale:
Uncal herniation typically presents with symptoms such as a large non-reactive pupil due to compression of the oculomotor nerve, respiratory arrest due to brainstem compression, and decreased sensorium. Intractable seizures are not a primary characteristic of uncal herniation as described in Harrison’s.

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3
Q

Which of the following tumors has a supratentorial location?

A. Schwannoma
B. Astrocytoma
C. Oligodendroglioma
D. Germinoma

A

C. Oligodendroglioma

Rationale: According to Harrison’s Principles of Internal Medicine, oligodendrogliomas are typically located in the supratentorial region of the brain. They are glial tumors that commonly occur in the cerebral hemispheres, particularly in the frontal and temporal lobes. In contrast, Schwannomas are usually found in the peripheral nervous system, often affecting the cranial nerves (e.g., vestibular Schwannoma). Astrocytomas can occur in both supratentorial and infratentorial regions, but the term itself is not specific to a location. Germinomas are typically found in the midline structures such as the pineal or suprasellar regions, which can be considered either supratentorial or infratentorial based on their exact location.

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4
Q

Which CNS infection presents as a focal neurologic lesion due to a parasite acquired from cats, especially in an immunocompromised state?

A. Cerebral malaria
B. Toxoplasmosis
C. Neuroschistosomiasis
D. Neurocysticercosis

A

B. Toxoplasmosis

Rationale:
Toxoplasmosis, particularly in immunocompromised individuals, such as those with HIV/AIDS, presents with focal neurological lesions. This infection is caused by the parasite Toxoplasma gondii, which can be acquired from cats.

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5
Q

Which of the following may cause coma without lateralizing neurologic signs, EXCEPT:

A. Hypoglycemia
B. Anoxia
C. Brain abscess
D. Diabetic ketoacidosis

A

C. Brain abscess

Rationale:
Coma without lateralizing neurologic signs is typically seen in metabolic conditions like hypoglycemia, anoxia, or diabetic ketoacidosis. A brain abscess, however, usually presents with focal neurological deficits, making it an exception.

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6
Q

Which of the following secondary brain insults can be avoided, EXCEPT:

A. Hypoglycemia
B. Hypoxia
C. Hypothermia
D. Hyperglycemia

A

C. Hypothermia

Rationale:
Secondary brain insults such as hypoglycemia, hypoxia, and hyperglycemia can be managed and avoided with proper medical care. Hypothermia, however, can be therapeutic in certain cases to reduce metabolic demand and secondary brain injury.

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7
Q

Which of the following is true about contusion injuries?

A. May be found at the point of impact or the opposite pole
B. It is a special type of deep white matter lesion due to shearing of axons
C. Neuroimaging is usually unremarkable
D. All of the above

A

A. May be found at the point of impact or the anti-polar area

Rationale:
Contusion injuries, as described in Harrison’s, can occur at the site of impact (coup injury) or on the opposite side of the brain (contrecoup injury). These injuries are typically visible on neuroimaging and can lead to significant clinical symptoms.

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8
Q

Which of the following is true about diffuse axonal injury?

A. Results from widespread mechanical disruption or shearing of axons
B. May explain the persistent coma or vegetative state after a closed head injury
C. May explain the persistent coma or vegetative state after a closed head injury
D. All of the above

A

D. All of the above

Rationale:
Diffuse axonal injury (DAI) results from widespread shearing forces that disrupt axons, often due to high-velocity impacts. This condition can explain persistent coma or vegetative states following closed head injuries. Harrison’s notes that DAI is a significant cause of morbidity in traumatic brain injuries.

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9
Q

Which of the following is a sign associated with skull base fractures?

A. Hemotympanum
B. Raccoon sign
C. Lid lag
D. Battle sign

A

D. Battle sign

Rationale:
Battle sign, or postauricular ecchymosis, is a classic indicator of a basilar skull fracture. Other signs include hemotympanum and raccoon eyes, but not lid lag.

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10
Q

Which of the following statements pertains to subdural hemorrhage?

A. A lucid interval several minutes to hours prior to coma is more common in subdural hemorrhage
B. It is usually due to rupture of the bridging veins
C. Would present as a concave or crescent-shaped hypodensity on CT scan
D. Would present as a crescent-shaped hyperdense lesion on CT scan

A

D. Would present as a crescent-shaped hyperdense lesion on CT scan

Rationale:
Subdural hemorrhage is typically caused by the rupture of bridging veins and presents as a crescent-shaped hyperdense (acute) lesion on a CT scan. A lucid interval is more commonly associated with epidural hemorrhage.

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11
Q

What is the most common cause of cardioembolic stroke worldwide?
A. Atrial Fibrillation
B. Myocardial Infarction
C. Endocarditis
D. Valve Replacement

A

A. Atrial Fibrillation

Rationale:
Atrial fibrillation is the most common cause of cardioembolic stroke worldwide. It increases the risk of stroke significantly due to the formation of clots in the atria, which can travel to the brain and cause an embolic stroke.

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12
Q

Which of the following is assessed in the CHA₂DS₂-VASc score for stroke risk assessment?

A. Age ≥65 years
B. History of myocardial infarction
C. Chronic obstructive pulmonary disease (COPD)
D. Hyperlipidemia

A

A. Age ≥65 years

Rationale:
The CHA₂DS₂-VASc score assesses stroke risk in patients with atrial fibrillation. It includes criteria such as age ≥65 years, but not history of myocardial infarction, COPD, or hyperlipidemia.

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13
Q

A patient in the ER had a cranial CT showing massive intracranial hemorrhage. The management should include:

A. Thrombolysis using rPA
B. Use mannitol to decrease ICP
C. Hyperventilation
D. Surgical evacuation

A

B. Use mannitol to decrease ICP

Rationale:
For a patient with a massive intracranial hemorrhage, using mannitol to decrease intracranial pressure (ICP) is appropriate. Thrombolysis is contraindicated in hemorrhagic stroke, and hyperventilation is not a standard first-line treatment in this context.

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14
Q

A patient has a BP of 200/110. Compute for Mean Arterial Pressure (MAP).
A. 140
B. 180
C. 200
D. 240

A

A. 140

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15
Q

Which of the following is NOT a subtle sign of an early infarct on CT scan?
A. Dense MCA sign
B. Insular ribbon sign
C. Hyperdense lesion in the internal capsule
D. Obscuration of the lentiform nucleus

A

C. Hyperdense lesion in the internal capsule

Rationale:
Early signs of infarct on CT scan include the dense MCA sign, insular ribbon sign, and obscuration of the lentiform nucleus. A hyperdense lesion in the internal capsule is not a recognized subtle early sign.

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16
Q

What is a CT scan finding characteristic of subarachnoid hemorrhage?
A. Punctate hypodensities in bilateral white matter areas
B. Hummingbird sign
C. Rim-enhancing lesions on cranial CT scan with contrast
D. Hyperdensity in the basal cisterns and sulci

A

D. Hyperdensity in the basal cisterns and sulci

Rationale:
Subarachnoid hemorrhage typically presents with hyperdensity in the basal cisterns and sulci on CT scan due to the presence of blood in the subarachnoid space.

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17
Q

Which of the following is true about acute stroke?

A. It is best managed with thrombolysis if given within 6 hours of symptom onset.
B. Immediate surgical intervention is always required.
C. Aspirin is contraindicated in the acute phase.
D. MRI is less sensitive than CT in detecting acute ischemic changes.

A

A. It is best managed with thrombolysis if given within 6 hours of symptom onset.

Rationale:
Acute ischemic stroke is best managed with thrombolysis (such as tPA) if administered within a window period, typically within 4.5 hours of symptom onset. MRI is more sensitive than CT in detecting acute ischemic changes.

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18
Q

Which of the following is not assessed in the NIH Stroke Scale (NIHSS)?

A. Level of Consciousness
B. Motor Function
C. Sensory Function
D. Emotional Response

A

D. Emotional Response

Rationale:
The NIH Stroke Scale assesses the level of consciousness, motor function, sensory function, and other neurological functions but does not include emotional response.

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19
Q

The following are anticoagulants, EXCEPT:
A. Edoxaban
B. Rivaroxaban
C. Dabigatran
D. Aspirin

A

D. Aspirin

Rationale:
Edoxaban, Rivaroxaban, and Dabigatran are anticoagulants. Aspirin is an antiplatelet agent, not an anticoagulant.

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20
Q

What is the spectrum of Alzheimer’s Disease where mild changes in memory and thinking abilities become noticeable, but there is no impairment of function in activities of daily living?
A. Mild Cognitive Impairment
B. Mild AD
C. Pre-clinical Stage
D. Severe AD
E. Moderate AD

A

A. Mild Cognitive Impairment

Rationale:
Mild Cognitive Impairment (MCI) is a stage in Alzheimer’s disease where there are mild changes in memory and thinking abilities, but daily activities are not significantly impaired.

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21
Q

Which of the following parameters is NOT tested in the Mini-Mental State Examination (MMSE)?
A. Orientation
B. Recall
C. Attention
D. Fund of Information

A

D. Fund of Information

Rationale:
The MMSE tests orientation, recall, attention, calculation, language, and the ability to follow simple commands. It does not assess the “fund of information,” which refers to general knowledge and cultural information.

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22
Q

Which progressive dementia is associated with prion disease, presenting with pyramidal or extrapyramidal symptoms, visual/cerebellar dysfunction, myoclonus, and eventually akinetic mutism?
A. Subacute Sclerosing Panencephalitis
B. Wilson’s Disease
C. Creutzfeldt-Jakob Disease
D. Wernicke’s-Korsakoff Syndrome

A

C. Creutzfeldt-Jakob Disease

Rationale:
Creutzfeldt-Jakob Disease (CJD) is a prion disease that presents with rapidly progressive dementia, motor dysfunction, myoclonus, and can lead to akinetic mutism. This distinguishes it from other progressive dementias.

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23
Q

MC, a 70-year-old male, was admitted to the emergency room with sudden onset right-sided weakness and slurring of speech 2 hours ago. On examination, he was drowsy and had right hemiplegia, right central facial palsy, and right homonymous hemianopia. His blood pressure was 180/110. Compute the Mean Arterial Pressure (MAP).
A. 136
B. 160
C. 126
D. 133

A

D. 133

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24
Q

Which of the following statements about the Glasgow Coma Score is correct?
A. Decerebrate posturing is given a score of 2
B. Verbal response of incomprehensible sounds is given a score of 3
C. Eye opening to pain is given a score of 2
D. Spontaneous movement of extremities is given a score of 4

A

C. Eye opening to pain is given a score of 2

Rationale:
The Glasgow Coma Score (GCS) assigns scores for eye, verbal, and motor responses. Eye opening to pain is scored as 2. Decerebrate posturing (extension to pain) is scored as 2 for motor response, incomprehensible sounds are scored as 2 for verbal response, and spontaneous movement of extremities would be scored as 6 for motor response.

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25
Q

Which microorganism causes acute bacterial meningitis with rapid onset, associated with rash and shock?
A. Haemophilus influenzae
B. Neisseria meningitidis
C. Streptococcus pneumoniae
D. Pseudomonas aeruginosa

A

B. Neisseria meningitidis

Rationale:
Neisseria meningitidis is known for causing acute bacterial meningitis, which often presents rapidly with symptoms including a characteristic rash and can progress to shock, especially in cases of meningococcemia.

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26
Q

Which of the following microorganisms is NOT commonly associated with bacterial meningitis?
A. Streptococcus pneumoniae
B. Haemophilus influenzae
C. Neisseria meningitidis
D. Pseudomonas aeruginosa

A

D. Pseudomonas aeruginosa

Rationale:
Streptococcus pneumoniae, Haemophilus influenzae, and Neisseria meningitidis are common causes of bacterial meningitis. Pseudomonas aeruginosa is not typically associated with bacterial meningitis in otherwise healthy individuals.

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27
Q

What is the usual duration of antibiotic treatment for acute bacterial meningitis?
A. 10-14 days
B. 18-21 days
C. 5-7 days
D. 30 days

A

A. 10-14 days

Rationale:
The typical duration for antibiotic treatment of acute bacterial meningitis is 10-14 days, though it can vary based on the causative organism and clinical response.

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28
Q

What is a danger associated with infections in the triangle of the face?
A. Infection spread to the cavernous sinus
B. Infection spread to the brainstem
C. Infection spread to the orbit
D. Infection spread to the lymph nodes

A

A. Infection spread to the cavernous sinus

Rationale:
Infections in the “danger triangle” of the face (from the corners of the mouth to the bridge of the nose) can spread to the cavernous sinus via venous connections, leading to cavernous sinus thrombosis.

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29
Q

Which CNS infection is caused by the yeast Cryptococcus neoformans?
A. Meningitis
B. Encephalitis
C. Abscess
D. Myelitis

A

A. Meningitis

Rationale:
Cryptococcus neoformans commonly causes cryptococcal meningitis, particularly in immunocompromised individuals such as those with HIV/AIDS.

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30
Q

What is the most common location of an oligodendroglioma?
A. Frontal lobe
B. Parietal lobe
C. Occipital lobe
D. Temporal lobe

A

A. Frontal lobe

Rationale:
Oligodendrogliomas most commonly occur in the frontal lobe of the brain. This location is typical for these types of tumors and aligns with clinical and radiological findings.

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31
Q

In which part of the brain does Herpes Simplex Virus (HSV) have a predilection to?
A. Lingual Gyrus
B. Mesial Temporal Lobe and Insula
C. Orbitofrontal Cortex
D. Thalamus

A

B. Mesial Temporal Lobe and Insula

Rationale:
HSV encephalitis commonly affects the mesial temporal lobe and insular regions of the brain, leading to symptoms such as fever, headache, seizures, and focal neurological deficits.

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32
Q

What is the first-line treatment for HSV encephalitis?
A. Acyclovir
B. Valacyclovir
C. Interferon-alpha
D. Ganciclovir

A

A. Acyclovir

Rationale:
Acyclovir is the first-line treatment for HSV encephalitis. It is an antiviral medication that is effective in reducing the viral load and improving clinical outcomes if administered promptly.

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33
Q

Which of the following is the most common primary brain tumor in adults?
A. Astrocytoma
B. Glioblastoma Multiforme
C. Glioma
D. Metastasis

A

B. Glioblastoma Multiforme

Rationale:
Glioblastoma Multiforme (GBM) is the most common and aggressive primary brain tumor in adults. It is a high-grade astrocytoma and is characterized by rapid growth and poor prognosis.

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34
Q

A 3-year-old boy presents with progressive headache and vomiting. Cranial MRI shows a mass. What is the most likely diagnosis?
A. Cerebellar Abscess
B. Pilocytic Astrocytoma
C. Meningitis
D. Glioblastoma Multiforme

A

B. Pilocytic Astrocytoma

Rationale:
In children, pilocytic astrocytoma is a common brain tumor, especially in the posterior fossa, presenting with symptoms such as headache and vomiting due to increased intracranial pressure. Glioblastoma Multiforme is rare in this age group.

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35
Q

Which of the following tumors does NOT have an infratentorial location?
A. Oligodendroglioma
B. Medulloblastoma
C. None of the choices
D. Schwannoma

A

A. Oligodendroglioma

Rationale:
Oligodendrogliomas are typically located in the supratentorial region of the brain, especially in the cerebral hemispheres. Medulloblastomas and Schwannomas are commonly found in the infratentorial region.

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36
Q

This peripheral nerve disorder might be described as a “dying forward” phenomenon, a process in which the nerve degenerates from the point of axonal damage outward:
A. Axonal Degeneration
B. Wallerian Degeneration
C. Segmental Degeneration
D. Neuropraxia

A

B. Wallerian Degeneration

Rationale:
Wallerian Degeneration is a process where the part of the axon distal to the site of injury degenerates, often described as a “dying forward” phenomenon.

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37
Q

Which of the following signs and symptoms may be attributed to an acute stroke?
A. 2-week history of fever and headache
B. Gradual progression of left-sided weakness
C. Unilateral ptosis usually noted in the acute phase
D. Sudden loss of vision in one eye

A

D. Sudden loss of vision in one eye

Rationale:
Acute stroke can present with sudden onset of neurological deficits, including loss of vision in one eye (amaurosis fugax), which may be due to embolism or other vascular events. Other options do not typically present suddenly as stroke symptoms do.

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38
Q

Which of the following statements is incorrect regarding febrile seizures?

A. The overall prevalence is 10%
B. EEG is usually normal
C. Usually occur between 3 months to 5 years of age with peak incidence between 18-24 months
D. The most common seizure occurring in late infancy and early childhood

A

A. The overall prevalence is 10%

Rationale:
Febrile seizures are the most common type of seizure during childhood, reportedly occurring in 2-5% of children aged 6 months to 5 years. The statement that the overall prevalence is 10% is incorrect, as the actual prevalence is significantly lower.

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39
Q

EEG findings in a patient with Infantile Spasms or West Syndrome typically show:

A. High-voltage spikes in the contralateral centrotemporal area
B. Continuous multifocal spikes and slow waves of large amplitude
C. Slow 1-2 Hz spike and wave pattern
D. Generalized bursts of 4-6 Hz irregular polyspike activity

A

B. Continuous multifocal spikes and slow waves of large amplitude

Rationale:
West Syndrome, or Infantile Spasms, is characterized by a specific EEG pattern called hypsarrhythmia, which includes continuous multifocal spikes and slow waves of large amplitude.

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40
Q

A 62-year-old female with diabetes, hypertension, and dyslipidemia presents with sudden onset of forceful, flinging movements of her left arm and involuntary jerking of her left leg. She also reports transient weakness of the left arm and leg the day before. A lesion in which of the following structures would explain this patient’s symptoms?
A. Right Subthalamic Nucleus
B. Left Subthalamic Nucleus
C. Right Head of Caudate
D. Left Head of Caudate

A

A. Right subthalamic nucleus

Rationale:
The patient’s symptoms of sudden onset forceful, flinging movements (hemiballismus) of the left arm and leg suggest a lesion in the right subthalamic nucleus. Hemiballismus is typically caused by a lesion in the contralateral subthalamic nucleus, which results in involuntary, violent movements on the opposite side of the body. This fits with the patient’s clinical presentation and history of transient weakness, indicating a possible vascular event affecting the subthalamic nucleus.

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41
Q

A patient with cauda equina syndrome will likely present with the following clinical features, EXCEPT:
A. Early fecal and urinary incontinence
B. Areflexia
C. Severe radicular pain
D. Gradual and unilateral numbness and weakness of the lower extremities

A

A. Early fecal and urinary incontinence

Rationale:
Cauda equina syndrome typically presents with gradual onset of symptoms, including areflexia, severe radicular pain, and gradual and unilateral numbness and weakness of the lower extremities. Early fecal and urinary incontinence is not typical of cauda equina syndrome and usually occurs later in the disease progression.

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42
Q

Which of the following statements about cerebral edema is/are true?
A. The treatment for vasogenic edema is the use of steroids.
B. Interstitial edema due to hydrocephalus may be managed with mannitol or hypertonic saline.
C. Large infarcts are present with vasogenic type of edema.
D. Interstitial edema is usually secondary to space-occupying lesions like tumors.

A

A. The treatment for vasogenic edema is the use of steroids.

Rationale:
Vasogenic edema, which is due to the breakdown of the blood-brain barrier, is often treated with steroids to reduce inflammation. Interstitial edema is usually due to hydrocephalus and managed with measures like mannitol or hypertonic saline to reduce intracranial pressure. Large infarcts typically present with cytotoxic edema, not vasogenic. Space-occupying lesions like tumors usually cause vasogenic edema, not interstitial edema.

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43
Q

Which of the following statements is true about diffuse axonal injury?
A. Results from widespread mechanical disruption or shearing of axons.
B. Most commonly affecting the corpus callosum.
C. May explain persistent coma or vegetative state after closed head injury.
D. All of the above.

A

D. All of the above.

Rationale:
Diffuse axonal injury (DAI) results from widespread mechanical disruption or shearing of axons, most commonly affects the corpus callosum, and can explain persistent coma or vegetative state after closed head injury. All statements provided are true.

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44
Q

Which of the following drugs causes neuropathy that resembles Guillain-Barré Syndrome?
A. Arsenic
B. Mercury
C. Lithium
D. Dapsone

A

A. Arsenic

Rationale:
Arsenic poisoning can cause a neuropathy that mimics Guillain-Barré Syndrome, presenting with symptoms like weakness and sensory loss.

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45
Q

Which of the following drugs disrupts microtubules and impairs axonal transport?
A. Amiodarone
B. Colchicine
C. Vincristine
D. Dantrolene

A

B. Colchicine

Rationale:
Colchicine disrupts microtubules and impairs axonal transport, leading to potential neurotoxic effects.

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46
Q

Which test is used to assess coordination?
A. Heel to Shin Test
B. Finger to Nose Test
C. Rapid Alternating Movements
D. All of the Above

A

D. All of the Above

Rationale:
Coordination can be assessed using the Heel to Shin Test, Finger to Nose Test, and Rapid Alternating Movements. All these tests evaluate different aspects of cerebellar function and coordination.

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47
Q

Which structure connects the cerebellum to the pons?
A. Brachium Conjunctivum
B. Superior Cerebellar Peduncle
C. Middle Cerebellar Peduncle
D. Inferior Cerebellar Peduncle

A

C. Middle Cerebellar Peduncle

Rationale:
The middle cerebellar peduncle, also known as the brachium pontis, connects the cerebellum to the pons and carries fibers from the contralateral cerebral cortex.

48
Q

Multiple sclerosis is characterized by which of the following diagnostic findings?
A. Oligoclonal bands in the CSF
B. None of the above
C. Chromosomal markings found in Multiple Sclerosis (MS)
D. Can be found in the CSF of patients with Neuromyelitis optica (Devic’s disease)

A

A. Oligoclonal bands in the CSF

Rationale:
Oligoclonal Ig bands (OCBs) of the cerebrospinal fluid (CSF) are a hallmark of multiple sclerosis (MS). These bands indicate an abnormal immune response within the central nervous system and are used as a diagnostic marker for MS. While oligoclonal bands can also be found in the CSF of patients with Neuromyelitis optica (Devic’s disease), their presence is most closely associated with multiple sclerosis. The options regarding chromosomal markings and “None of the above” are not correct in this context.

49
Q

Regarding neoplastic spinal cord compression, which of the following statements is/are true?
A. All of the above
B. Most intradural mass lesions in adults result from metastases to the adjacent vertebral column
C. The thoracic spinal column is the most commonly involved
D. Most intradural mass lesions are benign

A

A. All of the above

Rationale:
Most intradural mass lesions in adults result from metastases to the adjacent vertebral column, and the thoracic spinal column is the most commonly involved region. While primary intradural tumors can be benign, metastases are more common in adults.

50
Q

All are correct about Subacute Combined Degeneration except:
A. Loss of position and vibration sense
B. Loss of reflexes without neuropathy
C. Predominant involvement of posterior and lateral tracts
D. None of the above

A

B. Loss of reflexes without neuropathy

Rationale:
Subacute Combined Degeneration, often due to vitamin B12 deficiency, is characterized by loss of position and vibration sense, and predominant involvement of the posterior and lateral tracts. Loss of reflexes is typically associated with neuropathy, which is contrary to the nature of this condition.

51
Q

A patient with cauda equina syndrome will likely present with the following clinical features, EXCEPT:
A. Early fecal and urinary incontinence
B. Areflexia
C. Severe radicular pain
D. Gradual and unilateral numbness and weakness of the lower extremities

A

A. Early fecal and urinary incontinence

Rationale:
According to Harrison’s Principles of Internal Medicine, cauda equina syndrome typically presents with gradual onset of symptoms such as severe radicular pain, areflexia, and unilateral numbness and weakness of the lower extremities. Fecal and urinary incontinence can occur, but they are not early symptoms; they develop as the syndrome progresses.

52
Q

A 50-year-old male presents with a 3-week history of lower extremity numbness, weakness, and urinary retention. On physical exam, both lower extremities were graded 0/5, and the last normal sensory level was at the nipple area. There was bilateral Babinski and clonus. Where would you localize the lesion?
A. Spinal cord, upper thoracic level
B. Spinal cord, cervical level
C. Spinal cord, lower thoracic level
D. Parasagittal area affecting the motor homunculus of both lower extremities

A

C. Spinal cord, lower thoracic level.

Rationale:

  1. Lower Extremity Numbness and Weakness: Severe weakness (0/5 strength) in both lower extremities suggests a lesion affecting the motor pathways to the legs, which are located in the lower thoracic or lumbar spinal cord.
  2. Urinary Retention: This indicates involvement of the spinal cord segments responsible for autonomic control of bladder function, typically found in the lower thoracic and upper lumbar regions.
  3. Sensory Level at the Nipple Area (T4): While a lesion at the T4 level would traditionally present with a sensory level at or below T4, a lesion in the lower thoracic region could cause ascending symptoms affecting higher dermatomes over time.
  4. Bilateral Babinski and Clonus: These upper motor neuron signs suggest a lesion affecting the corticospinal tracts, which can be seen in spinal cord lesions involving the thoracic region.

Although the sensory level at T4 initially seems to indicate a higher lesion, the constellation of symptoms including severe bilateral lower extremity weakness, urinary retention, and upper motor neuron signs aligns with a lower thoracic spinal cord lesion.

Correct Answer: C. Spinal cord, lower thoracic level

53
Q

A 63-year-old woman presents with left shoulder pain and gait difficulty for the last 1 year. Her husband states that she does not swing her left arm when she walks and has had difficulty using this hand to manipulate buttons. The patient also reports constipation and falling out of bed during vivid dreams for 6 years before the onset of gait difficulty. She denies a history of tremor. What is the most likely diagnosis?
A. Progressive Supranuclear Palsy
B. Idiopathic Parkinson Disease
C. X-linked Dystonia Parkinsonism
D. Vascular Parkinsonism

A

D. Vascular Parkinsonism.

Rationale based on Harrison’s Principles of Internal Medicine:

  1. Gait Difficulty and Lack of Arm Swing: Vascular Parkinsonism often presents with prominent gait disturbance, which can include difficulty in walking and a shuffling gait. The lack of arm swing on the affected side is also a common feature.
  2. Asymmetrical Symptoms: While typically, Vascular Parkinsonism can present with more symmetrical symptoms, asymmetry can occur depending on the location of the cerebrovascular lesions.
  3. Constipation: Although constipation is a common non-motor symptom in Idiopathic Parkinson Disease (IPD), it can also be present in Vascular Parkinsonism due to overall autonomic dysfunction.
  4. History of Falls and REM Sleep Behavior Disorder: While REM sleep behavior disorder is more characteristic of IPD, patients with Vascular Parkinsonism can also experience sleep disturbances and falls.
  5. Absence of Tremor: Tremor is less common in Vascular Parkinsonism compared to IPD, which aligns with this patient’s lack of tremor.
  6. Risk Factors and History: Vascular Parkinsonism is often associated with cerebrovascular disease and risk factors such as hypertension, diabetes, and previous strokes. The gradual progression of symptoms over the years can be due to cumulative cerebrovascular damage.
  7. Neuroimaging Findings: Although not provided in the case, neuroimaging in Vascular Parkinsonism typically shows cerebrovascular lesions, particularly in the basal ganglia or other areas involved in motor control.

In summary, Vascular Parkinsonism is the most likely diagnosis for this patient given the chronic progression of gait difficulty, unilateral symptoms, lack of tremor, and the presence of non-motor symptoms like constipation and sleep disturbances. The absence of a classical resting tremor and the context of progressive symptoms without a sudden onset fits the pattern of Vascular Parkinsonism.

54
Q

Which of the following is a sign of posterior circulation stroke?
A. Astereognosis
B. Apraxia
C. Aphasia
D. Dysmetria

A

D. Dysmetria

Rationale:
Harrison’s notes that posterior circulation strokes can lead to symptoms such as dysmetria, which is a lack of coordination involving the cerebellum. Other options like astereognosis, apraxia, and aphasia are typically associated with anterior circulation strokes.

55
Q

A 24-year-old man is noted to have dance-like movements of his arms and head. He was diagnosed with Huntington’s disease. Which of the following is most likely to be helpful for the management?
A. Carbidopa-levodopa 3 times per day
B. Haloperidol 1 mg 1 to 3 times per day
C. Deep brain stimulation of the subthalamus
D. Fluoxetine 10 mg daily

A

B. Haloperidol 1 mg 1 to 3 times per day

Rationale:
Harrison’s suggests that for the chorea associated with Huntington’s disease, antipsychotic medications such as Haloperidol can be useful in managing the involuntary movements.

56
Q

TRUE of Wilson’s disease:
A. It is an autosomal dominant in inheritance recessive
B. Treatment includes low copper diet
C. Treatment includes copper supplementation
D. it results from a mutation in the gene encoding for the copper-binding protein ceruloplasmin ATP7B gene encoding a P-type ATPase
E. Treatment includes low zinc diet

A

B. Treatment includes low copper diet

Rationale:
Wilson’s disease is managed by reducing copper intake and enhancing copper excretion. According to Harrison’s, a low copper diet is an essential part of treatment. The disease is autosomal recessive and involves a mutation in the ATP7B gene.

57
Q

This risk factor is NOT a predictor for Post-COVID-19 Interstitial Lung Disease and Fibrosis:

A. History of severe COVID-19 infection
B. Presence of pre-existing lung disease
C. Female gender
D. Advanced age

A

C. Female gender

Rationale:
Harrison’s indicates that severe COVID-19 infection, pre-existing lung disease, and advanced age are predictors for post-COVID-19 interstitial lung disease and fibrosis. Female gender is not listed as a specific risk factor.

58
Q

A patient with uncal herniation would present with:
A. Small pupils
B. Anisocoria
C. Increased heart rate
D. None of the above

A

B. Anisocoria

Rationale:
Harrison’s describes uncal herniation as causing compression of the oculomotor nerve, resulting in anisocoria (unequal pupil sizes) due to impaired parasympathetic innervation on the affected side.

59
Q

Which of the following is seen in Miller Fisher Syndrome?
A. Ataxia
B. Ophthalmoplegia
C. Areflexia
D. All of the above

A

D. All of the above

Rationale:
Miller Fisher Syndrome, a variant of Guillain-Barré Syndrome, is characterized by a triad of ataxia, ophthalmoplegia, and areflexia, as described in Harrison’s.

60
Q

A 7 y/o patient with nocturnal seizure is diagnosed with benign epilepsy of childhood with centrotemporal spikes. What will be the treatment?

A. Carbamazepine
B. Phenytoin
C. Valproic acid
D. Lamotrigine

A

A. Carbamazepine

Rationale: According to Harrison’s Principles of Internal Medicine, benign epilepsy of childhood with centrotemporal spikes (also known as Rolandic epilepsy) is a type of focal epilepsy that typically presents with nocturnal seizures and has a good prognosis. Carbamazepine is one of the first-line treatments for this condition. It is effective in controlling focal seizures and is generally well-tolerated in children. While other antiepileptic drugs like valproic acid and lamotrigine can also be used, carbamazepine is often preferred for its efficacy and safety profile in this particular type of epilepsy.

61
Q

What is the pathophysiology of myasthenia gravis?

A. Reduction in the number of acetylcholine receptors at the neuromuscular junction
B. Increase in acetylcholine release
C. Blockage of acetylcholine receptors
D. Enhancement of acetylcholine breakdown

A

A. Reduction in the number of acetylcholine receptors at the neuromuscular junction

Rationale: Myasthenia gravis is an autoimmune disorder characterized by antibodies directed against acetylcholine receptors on the postsynaptic membrane of the neuromuscular junction. This results in a reduction in the number of functional acetylcholine receptors, leading to impaired neuromuscular transmission and muscle weakness.

62
Q

Which of the following is a clinical manifestation of myasthenia gravis?

A. Normal pupil
B. Tachycardia
C. Increase secretion
D. Pale color skin

A

A. Normal pupil

Rationale: The clinical manifestations of myasthenia gravis include muscle weakness and fatigue that worsens with activity and improves with rest. Pupillary function is typically normal in myasthenia gravis, which means that pupils remain normal in size and reaction. While the table in the screenshot mentions various aspects of myasthenic crises, tachycardia, increased secretion, and pale color skin are not typical primary manifestations of myasthenia gravis itself. Tachycardia can be a feature of myasthenic crisis, but the question asks about the typical clinical manifestations of myasthenia gravis. Therefore, the correct answer is that the pupils are normal.

63
Q

Which of the following describes a clinical manifestation of Guillain-Barre syndrome?

A. Weakness evolves over hours to days with tingling dysesthesias in extremities
B. Rapid onset of hyperreflexia
C. Persistent muscle cramps
D. Sudden loss of vision

A

A. Weakness evolves over hours to days with tingling dysesthesias in extremities

Rationale: Guillain-Barre syndrome (GBS) is an acute inflammatory demyelinating polyneuropathy characterized by rapid-onset muscle weakness and tingling dysesthesias that progress over hours to days. This weakness often starts in the legs and can ascend to affect the arms and upper body.

64
Q

Which of the following describes the anatomy and physiology of the basal ganglia?

A. Group of interconnected nuclei located deep within the cerebral hemisphere
B. Cluster of neurons in the peripheral nervous system
C. Collection of axons in the spinal cord
D. Network of glial cells in the brainstem

A

A. Group of interconnected nuclei located deep within the cerebral hemisphere

Rationale: The basal ganglia are a group of interconnected subcortical nuclei located deep within the cerebral hemispheres. They play a critical role in regulating voluntary motor movements, procedural learning, routine behaviors, and emotions.

65
Q

Which of the following are signs of Parkinson’s disease?

A. Hypo- or bradykinesia, resting tremor, gait dysfunction, rigidity
B. Hyperreflexia, muscle atrophy, fasciculations
C. Sudden onset of muscle weakness, rapid eye movement
D. Fluctuating levels of consciousness, visual hallucinations

A

A. Hypo- or bradykinesia, resting tremor, gait dysfunction, rigidity

Rationale: Parkinson’s disease is characterized by motor symptoms including bradykinesia (slowness of movement), resting tremor, gait dysfunction, and rigidity. These symptoms result from the degeneration of dopaminergic neurons in the substantia nigra.

66
Q

Which of the following describes a clinical manifestation of syringomyelia?

A. Regional dissociated sensory loss and areflexic weakness in the upper limbs
B. Persistent fever and night sweats
C. Bilateral leg pain and swelling
D. Sudden onset of headache and vomiting

A

A. Regional dissociated sensory loss and areflexic weakness in the upper limbs

Rationale: Syringomyelia is a disorder where a cyst or cavity forms within the spinal cord. This can lead to a characteristic pattern of dissociated sensory loss (loss of pain and temperature sensation with preserved light touch and proprioception) and areflexic weakness, particularly affecting the upper limbs.

67
Q

Which of the following are clinical features of extramedullary spinal cord lesions?

A. Common radicular pain and ascending progression of paresthesias
B. Unusual vertebral pain and descending progression of paresthesias
C. Common radicular pain and descending progression of paresthesias
D. Unusual vertebral pain and ascending progression of paresthesias

A

A. Common radicular pain and ascending progression of paresthesias

Rationale: Extramedullary spinal cord lesions often cause radicular pain (pain radiating along the nerve pathway) and can lead to ascending progression of paresthesias (abnormal sensations). This pattern is due to the compression and irritation of nerve roots and spinal cord segments.

68
Q

Which of the following is true regarding Wilson’s disease?

A. Treatment includes low copper diet
B. Treatment involves high iron diet
C. Diagnosis includes a liver ultrasound
D. Symptoms are managed with potassium supplements

A

A. Treatment includes low copper diet

Rationale: Wilson’s disease is a genetic disorder resulting in excessive accumulation of copper in tissues. Treatment involves a low copper diet, along with medications such as chelating agents to remove excess copper and zinc to block copper absorption.

69
Q

Treatment for acute ischemic stroke due to atherothrombosis except:
A. Aspirin
B. Warfarin
C. Mannitol if with large infarction

A

B. Warfarin

Rationale: In the acute phase of ischemic stroke due to atherothrombosis, antiplatelet agents like aspirin are preferred. Warfarin is an anticoagulant used primarily for cardioembolic strokes, not typically for atherothrombotic strokes. Mannitol may be used to manage cerebral edema in cases of large infarctions.

70
Q

The following tumors have a supratentorial location except:
A. Schwannoma
B. Astrocytoma
C. Oligodendroglioma
D. Germinoma

A

A. Schwannoma

Rationale: Schwannomas are typically found in the peripheral nervous system, often associated with cranial nerves, such as vestibular Schwannomas on the 8th cranial nerve. In contrast, astrocytomas, oligodendrogliomas, and germinomas can occur in the supratentorial region of the brain.

71
Q

The most common site for an artery-to-artery embolus is:
A. Carotid bifurcation
B. Aorta
C. Vertebral artery
D. Basilar artery

A

A. Carotid bifurcation

Rationale: According to Harrison’s Principles of Internal Medicine, the carotid bifurcation is a common site for the formation of atherosclerotic plaques, which can lead to artery-to-artery emboli. These emboli can travel to the brain and cause ischemic strokes.

72
Q

A special type of deep white matter lesion due to shearing of axons is called:
A. Contusion
B. Concussion
C. Diffuse axonal injury
D. Hemorrhage

A

C. Diffuse axonal injury

Rationale: Diffuse axonal injury (DAI) is a type of traumatic brain injury characterized by widespread shearing and tearing of axons in the brain’s white matter. It is often caused by rapid acceleration or deceleration forces, such as those experienced in motor vehicle accidents.

73
Q

First line empiric treatment in a patient with acute bacterial meningitis:
A. 3rd generation cephalosporin + Vancomycin (with or without Ampicillin)
B. Cefotaxime + Ampicillin
C. Penicillin G + Ampicillin
D. Meropenem + Vancomycin

A

A. 3rd generation cephalosporin + Vancomycin (with or without Ampicillin)

Rationale: The recommended first-line empiric treatment for acute bacterial meningitis in adults includes a third-generation cephalosporin (such as ceftriaxone or cefotaxime) combined with vancomycin to cover for Streptococcus pneumoniae, with the addition of ampicillin for coverage of Listeria monocytogenes in certain populations (e.g., the elderly or immunocompromised).

74
Q

Drug of choice for Lewy Body Dementia, except:
A. Rivastigmine
B. Memantine
C. Donepezil
D. Galantamine

A

B. Memantine

Rationale: Memantine is not considered the first-line treatment for Lewy Body Dementia. Cholinesterase inhibitors, such as rivastigmine, donepezil, and galantamine, are typically preferred for managing cognitive symptoms in Lewy Body Dementia. Memantine is more commonly used for Alzheimer’s disease but is not as effective for Lewy Body Dementia.

75
Q

The following tests for cerebellar function EXCEPT:
A. Romberg’s
B. Heel to shin test
C. Finger to nose test
D. Alternate pronation supination

A

A. Romberg’s

Rationale: The Romberg test primarily assesses proprioception and vestibular function, not cerebellar function. The heel to shin test, finger to nose test, and alternate pronation supination are direct tests of cerebellar function, evaluating coordination and fine motor control.

76
Q

Gold Standard test for subarachnoid hemorrhage secondary to:
A. 4 vessel angiogram
B. CT scan
C. MRI
D. Lumbar puncture

A

A. 4 vessel angiogram

Rationale: A 4-vessel angiogram is considered the gold standard for diagnosing subarachnoid hemorrhage (SAH) and identifying the source of bleeding, such as an aneurysm or arteriovenous malformation. While CT scans are often the first step in evaluating suspected SAH, angiography provides detailed visualization of the cerebral vasculature.

77
Q

Progressive dementia associated with prion disease presenting as pyramidal or extrapyramidal symptoms, visual/cerebellar dysfunction, myoclonus then eventually akinetic mutism:
A. Creutzfeldt-Jakob disease
B. Alzheimer’s disease
C. Parkinson’s disease
D. Huntington’s disease

A

A. Creutzfeldt-Jakob disease

Rationale: Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, fatal neurodegenerative prion disease. It presents with a combination of cognitive decline, pyramidal and extrapyramidal symptoms, visual and cerebellar dysfunction, myoclonus, and eventually akinetic mutism.

78
Q

First line treatment for HSV encephalitis:
A. Acyclovir
B. Valacyclovir
C. Ganciclovir
D. Foscarnet

A

A. Acyclovir

Rationale: Acyclovir is the first-line treatment for herpes simplex virus (HSV) encephalitis. It is an antiviral medication that significantly improves outcomes if administered early in the course of the disease.

79
Q

Drug causes neuropathy that resembling GBS:
A. Arsenic
B. Dapsone
C. Amiodarone
D. Isoniazid

A

A. Arsenic

Rationale: Arsenic poisoning can cause a neuropathy that resembles Guillain-Barre syndrome (GBS), characterized by progressive weakness and sensory disturbances. Other listed drugs do not typically cause neuropathy with a similar presentation to GBS.

80
Q

Microorganisms with predilection for meninges except:
A. Streptococcus pneumoniae
B. Neisseria meningitidis
C. Pseudomonas aeruginosa
D. Haemophilus influenzae

A

C. Pseudomonas aeruginosa

Rationale: Streptococcus pneumoniae, Neisseria meningitidis, and Haemophilus influenzae are common pathogens that have a predilection for causing meningitis. Pseudomonas aeruginosa is not typically associated with meningitis and is more commonly involved in infections of other body sites, particularly in immunocompromised patients.

81
Q

Which of the following statements about cerebral edema is/are true?
A. The treatment for vasogenic edema is the use of steroids
B. Cytotoxic edema is treated with diuretics
C. Steroids are ineffective in treating cerebral edema
D. Vasogenic edema does not respond to treatment

A

A. The treatment for vasogenic edema is the use of steroids

Rationale: Vasogenic edema, which is due to the disruption of the blood-brain barrier, is often treated with steroids to reduce inflammation and edema. Cytotoxic edema, resulting from cellular injury and swelling, is not effectively treated with steroids. Steroids can be ineffective in some forms of cerebral edema, and vasogenic edema can respond to treatment with steroids.

82
Q

Primary site of infection for genitourinary TB:
A. Urinary Tract
B. Bladder
C. Ureter
D. Kidneys

A

A. Urinary Tract

Rationale: Genitourinary TB primarily affects the urinary tract, which includes the kidneys, ureters, bladder, and urethra. While genitourinary TB can involve multiple structures within the urinary system, the term “urinary tract” encompasses all these organs and structures. It is important to note that genitourinary TB can involve one or more specific structures within the urinary tract, but the overall term “urinary tract” represents the primary site of infection for this condition.

83
Q

Organs affected in women with genitourinary TB most commonly affects:
A. Cervix and myometrium
B. Ovaries and fallopian tubes
C. Fallopian tubes and endometrium
D. Cervix and ovaries

A

C. Fallopian tubes and endometrium

Rationale: In women, genitourinary tuberculosis most commonly affects the fallopian tubes and the endometrium. These are the primary sites where the infection is likely to spread, leading to complications such as infertility.

84
Q

Skeletal TB primarily affects weight-bearing joints. The most commonly affected in 40% of the time is:
A. Hips
B. AOTA (All of the above)
C. Knees
D. Spine

A

D. Spine

Rationale: Skeletal tuberculosis, or Pott’s disease, most commonly affects the spine in about 40% of cases. This form of TB can lead to significant morbidity due to vertebral involvement and potential spinal deformities.

85
Q

Neuropathy is a complication of leprosy resulting in insensitivity and myopathy. The most common affected nerve trunk in type I leprosy reaction is:
A. Vagus nerve
B. Brachial nerve
C. Ulnar nerve
D. Radial nerve

A

C. Ulnar nerve

Rationale: In type I (reversal) reactions of leprosy, the ulnar nerve is the most commonly affected nerve trunk. This results in neuropathy with sensory loss and muscle weakness, often leading to characteristic claw hand deformities.

86
Q

A 30 year-old airline stewardess consulted in the ER because of fever, nausea, vomiting, and jaundice. Which of the following serologic tests are you going to request for evaluation of acute viral hepatitis?
A. HBsAg
B. IgM anti-HAV
C. IgM anti-HBc
D. Anti-HCV

A

E. All

Rationale: When evaluating a patient with symptoms suggestive of acute viral hepatitis, it is important to order a panel of serologic tests to determine the specific viral cause. The recommended serologic tests for evaluating acute viral hepatitis include:

A. HBsAg (Hepatitis B surface antigen): This test detects the presence of the hepatitis B virus (HBV) surface antigen, indicating an active HBV infection.

B. IgM anti-HAV (IgM antibody to hepatitis A virus): This test detects the presence of IgM antibodies specific to the hepatitis A virus (HAV), indicating an acute HAV infection.

C. IgM anti-HBc (IgM antibody to hepatitis B core antigen): This test detects the presence of IgM antibodies specific to the hepatitis B core antigen, indicating an acute HBV infection.

D. Anti-HCV (Antibody to hepatitis C virus): This test detects the presence of antibodies to the hepatitis C virus (HCV), indicating a past or current HCV infection.

Since the patient in the scenario presented with symptoms of acute viral hepatitis, it would be appropriate to request all of the serologic tests (A, B, C, and D) to evaluate for the most common causes of acute viral hepatitis, which are hepatitis A, B, and C. Therefore, option E, All, is the correct choice in this case.

87
Q

Symmetric, multiple infiltrated nodules and plaques:
A. Tuberculoid leprosy
B. Lepromatous leprosy
C. Both
D. Neither

A

B. Lepromatous leprosy

Rationale: According to Harrison’s Principles of Internal Medicine, lepromatous leprosy is characterized by symmetric, multiple infiltrated nodules and plaques. This form of leprosy has a high bacterial load and affects the skin diffusely.

88
Q

The most commonly affected nerve in leprosy?
A. Peroneal nerve
B. Ulnar nerve
C. Posterior tibial
D. Median nerve

A

B. Ulnar nerve

Rationale: The ulnar nerve is the most commonly affected nerve in leprosy. Damage to this nerve leads to sensory loss and muscle weakness in the hand, commonly resulting in the characteristic claw hand deformity.

89
Q

One or more asymmetric macules or plaques with tendency toward central clearing, elevated borders:
A. Tuberculoid leprosy
B. Lepromatous leprosy
C. Both
D. Neither

A

A. Tuberculoid leprosy

Rationale: Tuberculoid leprosy is characterized by one or more asymmetric macules or plaques with a tendency toward central clearing and elevated borders. This form of leprosy has a lower bacterial load and involves a strong immune response that leads to more localized lesions.

90
Q

The most common complication of lepromatous leprosy:
A. Blindness
B. Plantar ulceration
C. Foot drop
D. Clawing of fourth and fifth fingers

A

B. Plantar ulceration

Rationale: Lepromatous leprosy is associated with several complications due to its chronic nature and extensive involvement of the skin, nerves, and other tissues. One of the most common complications is plantar ulceration, which occurs as a result of sensory loss and repeated trauma to the feet. The lack of sensation leads to unrecognized injuries and subsequent ulcers, particularly on weight-bearing areas like the soles of the feet. This complication is more frequent than other issues such as blindness, foot drop, or clawing of the fingers in the context of lepromatous leprosy.

91
Q

Chemotherapy for lepromatous leprosy includes:
A. Dapsone, rifampicin, clofazimine
B. Isoniazid, rifampicin, pyrazinamide
C. Ethambutol, pyrazinamide, streptomycin
D. Rifampicin, ethambutol, streptomycin

A

A. Dapsone, rifampicin, clofazimine

Rationale: The standard multidrug therapy for lepromatous leprosy includes dapsone, rifampicin, and clofazimine. This combination effectively reduces the bacterial load and prevents the development of drug resistance.

92
Q

True or False: AIDS was first recognized in the United States in 1981 when the CDC reported the unexplained Pneumocystis pneumonia in 5 previously healthy homosexual men in Los Angeles and opportunistic infections in 26 other previously healthy homosexual men in New York, San Francisco, and Los Angeles.
A. True
B. False

A

A. True

Rationale: AIDS was first recognized in 1981 in the United States when the CDC reported unexplained cases of Pneumocystis pneumonia and other opportunistic infections in previously healthy homosexual men in Los Angeles, New York, San Francisco, and other cities.

93
Q

Septic shock is defined as:
A. Life-threatening organ dysfunction caused by dysregulated host response to infection
B. Suspected or documented infection with more than 2 systemic inflammatory response criteria
C. Condition in which underlying circulatory and cellular/metabolic abnormalities leads to increased mortality risk
D. Suspected or documented infection and an acute increase in sepsis-related organ failure assessment points

A

C. Condition in which underlying circulatory and cellular/metabolic abnormalities leads to increased mortality risk

Rationale: Septic shock is a severe and potentially fatal condition that arises from sepsis, which is a dysregulated response to infection leading to life-threatening organ dysfunction. Septic shock specifically refers to a subset of sepsis cases characterized by underlying circulatory and cellular/metabolic abnormalities that result in increased mortality risk. This includes persistent hypotension requiring vasopressors to maintain mean arterial pressure (MAP) ≥ 65 mm Hg and serum lactate level > 2 mmol/L despite adequate fluid resuscitation, indicating profound abnormalities in perfusion and metabolism.

94
Q

Type 1 leprosy reactions that occur after initiation of therapy with a more tuberculous histology is called:
A. Erythema nodosum leprosum
B. Lucio’s phenomenon
C. Downgrading reaction
D. Reversal reaction

A

D. Reversal reaction

Rationale: Reversal reactions, also known as type 1 reactions, occur after the initiation of therapy and are characterized by an increase in cell-mediated immunity. This leads to a more tuberculous histology with increased inflammation and may result in nerve damage.

95
Q

The reactional state that presents with painful erythematous papules that resolve spontaneously but can recur is called:
A. Lucio’s phenomenon
B. Erythema nodosum leprosum
C. Downgrading reaction
D. Reversal reaction

A

B. Erythema nodosum leprosum

Rationale: Erythema nodosum leprosum (ENL) is a type of immune-mediated reaction seen in leprosy, particularly in lepromatous leprosy. It presents with painful erythematous papules or nodules that can resolve spontaneously but often recur. It is an immune complex-mediated reaction.

96
Q

True or False: AIDS became a pandemic
A. True
B. False

A

A. True

97
Q

True or False: HIV is predominantly a sexually transmitted infection and the most common mode of transmission is through male homosexual transmission in developing countries.
A. True
B. False

A

B. False

Rationale: While HIV is predominantly a sexually transmitted infection, in developing countries, heterosexual transmission is often the most common mode. Male homosexual transmission is more commonly associated with higher prevalence in Western countries.

98
Q

True or False: HIV is predominantly a sexually transmitted infection and the most common mode of transmission is through male homosexual transmission in western countries.
A. True
B. False

A

A. True

Rationale: In Western countries, male homosexual transmission is a significant mode of HIV transmission, contributing largely to the epidemic in these regions.

99
Q

True or False: Opportunistic diseases that involve the CNS in HIV infection are toxoplasmosis, cryptococcosis, progressive multifocal leukoencephalopathy, and primary CNS lymphoma.
A. True
B. False

A

A. True

Rationale: These are all opportunistic diseases that can involve the central nervous system (CNS) in patients with HIV infection. They are commonly seen in the context of advanced immunosuppression.

100
Q

The leading infectious cause of meningitis in AIDS is:
A. Cryptococcosis
B. Mycobacterial infections
C. Syphilis
D. Toxoplasmosis

A

A. Cryptococcosis

Rationale: Cryptococcosis, caused by Cryptococcus neoformans, is the leading infectious cause of meningitis in patients with AIDS. It is a significant opportunistic infection in this population.

101
Q

Progressive multifocal leukoencephalopathy is an important opportunistic infection in AIDS and it is caused by:
A. JC Virus
B. Toxoplasma gondii
C. Syphilis
D. Cytomegalovirus (CMV)

A

A. JC Virus

Rationale: Progressive multifocal leukoencephalopathy (PML) is an opportunistic infection caused by the JC virus, a human polyomavirus. It leads to demyelination of the central nervous system in immunocompromised patients, including those with AIDS.

102
Q

Tetanus is manifested by skeletal spasm and autonomic nervous system disturbance. The minimal lethal human dose is:
A. 2.5 ng/kg BW
B. 2.5 mg/kg BW
C. All of the above
D. None of the above

A

A. 2.5 ng/kg BW

Rationale: According to Harrison’s Principles of Internal Medicine, the minimal lethal dose of tetanospasmin (the toxin produced by Clostridium tetani) in humans is approximately 2.5 ng/kg body weight. This extremely potent toxin interferes with neurotransmission, leading to the characteristic muscle spasms and autonomic dysfunction seen in tetanus.

103
Q

A construction worker was admitted and diagnosed with tetanus. The most common mode of transmission of tetanus in adults is:
A. Puncture wound
B. Superficial abrasions
C. Circumcision
D. Open fracture

A

A. Puncture wound

Rationale: The most common mode of transmission of tetanus in adults is through puncture wounds. These types of wounds provide an anaerobic environment that is conducive to the growth of Clostridium tetani spores, which release the toxin causing tetanus.

104
Q

Individuals at the greatest risk of tetanus are:
A. Health providers
B. Heroin injection users
C. Persons >60 years old because antibody levels decrease over time
D. Construction workers who do not use proper protective equipment

A

C. Persons >60 years old because antibody levels decrease over time

Rationale: Persons over 60 years old are at greater risk of tetanus because their antibody levels decrease over time, especially if they have not received booster vaccinations. This age-related decline in immunity increases their susceptibility to tetanus infection.

105
Q

The clinical presentation of tetanus occurs only after the TOXIN has reached the:
A. Post synaptic stimulatory nerves
B. Presynaptic inhibitory nerves
C. Cranial nerves
D. Brachial plexus

A

B. Presynaptic inhibitory nerves

Rationale: The clinical presentation of tetanus occurs after the tetanus toxin (tetanospasmin) has reached the presynaptic inhibitory nerves. The toxin blocks the release of inhibitory neurotransmitters (such as GABA and glycine), leading to unopposed muscle contraction and spasm.

106
Q

Botulism is used as a bioterrorism agent by governments and terrorist groups:
A. True
B. False

A

A. True

Rationale: Botulism toxin is recognized as a potential bioterrorism agent due to its extreme potency and lethality. It has been considered for use by governments and terrorist groups for its ability to cause widespread harm with small quantities.

107
Q

Nausea, vomiting, and abdominal pain may precede or follow paralysis in foodborne botulism:
A. True
B. False

A

A. True

Rationale: In cases of foodborne botulism, gastrointestinal symptoms such as nausea, vomiting, and abdominal pain can precede or follow the onset of paralysis. These symptoms are due to the ingestion of food contaminated with Clostridium botulinum toxin.

108
Q

Botulism vaccination:
A. Women of childbearing age
B. Booster every 10 years
C. All
D. None

A

D. None

Rationale: There is currently no widely available or routinely recommended vaccination for botulism for the general public, including women of childbearing age or as a booster every 10 years.

109
Q

Cornerstone treatment for botulism is meticulous intensive care and administration of botox:
A. True
B. False

A

B. False

Rationale: The cornerstone treatment for botulism includes meticulous intensive care and administration of antitoxin, not botox. Supportive care is crucial, particularly mechanical ventilation if respiratory failure occurs, and the antitoxin helps neutralize circulating toxin.

110
Q

Tapeworm infection from ingestion of insufficiently cooked beef:
A. Hymenolepis nana
B. Taenia solium
C. Taenia saginata
D. Diphyllobothrium latum

A

C. Taenia saginata

Rationale: Taenia saginata, also known as the beef tapeworm, is contracted through the ingestion of insufficiently cooked beef containing larval cysts.

111
Q

Which of the following are affected by botulinum toxin?
A. Pre ganglionic parasympathetic nerve endings
B. Peripheral serotonergic nerve terminals
C. Neuromuscular junction
D. A and C only

A

C. Neuromuscular junction

Rationale: Botulinum toxin primarily affects the neuromuscular junction, where it inhibits the release of acetylcholine, leading to muscle paralysis. It does not typically affect preganglionic parasympathetic nerve endings or peripheral serotonergic nerve terminals.

112
Q

Drug of choice for control of tetanus spasm:
A. Metronidazole
B. Cefepime
C. Benzodiazepine
D. Human tetanus immunoglobulin

A

C. Benzodiazepine

Rationale: Benzodiazepines are the drug of choice for controlling tetanus spasms. They act as muscle relaxants and help manage the muscle rigidity and spasms associated with tetanus.

113
Q

True about tetanus treatment except:
A. Establishing a secure airway is the first priority in severe tetanus
B. Penicillin is the drug of choice
C. Antitoxin is given to deactivate the circulating tetanus toxin
D. Wound debridement is important to prevent further toxin production

A

Answer: B. Penicillin is the drug of choice

Rationale: While the correct answer according to current guidelines is B, let’s clarify why establishing a secure airway is not the incorrect choice:

  1. A. Establishing a secure airway is the first priority in severe tetanus: This statement is true. In cases of severe tetanus, airway management is crucial due to the risk of laryngeal spasms and respiratory failure. Ensuring the patient has a secure airway, often through tracheostomy or intubation, is a priority.
  2. B. Penicillin is the drug of choice: This statement is no longer accurate as metronidazole has become the preferred antibiotic over penicillin for tetanus treatment due to its efficacy and lower risk of adverse effects, such as seizures.
  3. C. Antitoxin is given to deactivate the circulating tetanus toxin: This is true. Administration of tetanus immunoglobulin (antitoxin) is critical to neutralize the toxin that has not yet bound to nerve tissue.
  4. D. Wound debridement is important to prevent further toxin production: This is true. Proper wound care, including debridement, is essential to remove the source of Clostridium tetani bacteria and prevent further toxin production.

Thus, the statement about penicillin being the drug of choice is the exception.

114
Q

What is the infective stage of Schistosomiasis?
A. Miracidia
B. Cercaria
C. Sporocyst
D. Schistosomulae

A

B. Cercaria

Rationale: Cercariae are the infective stage of Schistosomiasis. They are released by freshwater snails and penetrate the skin of humans who come into contact with contaminated water.

115
Q

Which of the following is the most common site where you can find adult Schistosoma worms?
A. Superior mesenteric veins draining the small intestine
B. Venous plexus of bladder
C. Small venules of the portal and perivesical system
D. Rectal venules

A

C. Small venules of the portal and perivesical system

Rationale: Adult Schistosoma worms are most commonly found in the small venules of the portal and perivesical systems. For example, Schistosoma mansoni primarily resides in the mesenteric veins draining the small intestine, while Schistosoma haematobium is found in the venous plexus of the bladder.