Nervous System Flashcards

1
Q

A baby born with a small skin defect on her lower back could not move her legs. What is the most likely cause of her congenital paralysis? What is the blood test that is used for prenatal diagnosis of this disease?

A

Neural tube defect (spina bifida). The maternal serum screen (triple screen or quad screen) is performed on the mother during her second trimester to screen for a variety of problems and includes an AFP (alpha-fetoprotein) test. An increased level of AFP in the mother’s blood has been associated with an increased risk of an open NTD in the baby.

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2
Q

A 60-year old man with hypertension suddenly developed an excruciating headache, collapsed, and became unconscious. What is the cause of this man’s collapse?

A

Saccular (berry) aneurysm

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3
Q

A 20-year old woman had a car accident. When she was removed from the car, she could not move her legs. Is she paralyzed for life?

A

Spinal cord injury occurs when the bony protection surrounding the cord is damaged by way of fractures, dislocation, burst; compression, hyperextension or hyperflexion. A spinal cord injury — damage to any part of the spinal cord or nerves at the end of the spinal canal — often causes permanent changes in strength, sensation and other body functions below the site of the injury.

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4
Q

A 30-year old woman had a bout of flu accompanied by fever and nasal congestion. On the third day of her disease, she experienced severe headache, blurry vision and neck rigidity. What is the cause of these symptoms?

A

Viral meningitis is the most common viral disease in the central nervous system.

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5
Q

The family of a 70-year old man noticed that he had become very forgetful. He could not remember anything and was dismissed from his office job. What is the most likely diagnosis?

A

Alzheimer disease

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6
Q

A small proteinaceous infectious disease-causing agent that is believed to be the smallest infectious particle. Is not bacterial, fungal, or viral in nature and contains no genetic material. These proteins can fold in multiple, structurally distinct ways, at least one of which is transmissible to other proteins:

A

Prion

Mad cow disease, Creutzfeldt-Jakob disease, and kuru.

Characterized pathologically by the presence of “spongiform degeneration”.

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7
Q

Can cause compression of the brain stem leading to loss of breathing and heart rate:

A

Hematomas

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8
Q

Part of the brain responsible for emotion, reasoning, speech, and movement (motor cortex and sensory cortex):

A

Frontal lobe

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9
Q

Part of the brain that controls movement:

A

Motor cortex

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10
Q

Part of the brain responsible for sensation:

A

Sensory cortex

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11
Q

Part of the brain responsible for reactions and recognition:

A

Parietal lobe

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12
Q

Part of the brain responsible for memory, hearing, and language:

A

Temporal lobe

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13
Q

Part of the brain responsible for performing the basic functions of life such as breathing and pumping blood throughout the body.

A

Brain stem

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14
Q

Part of the brain that governs posture and balance:

A

Cerebellum

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15
Q

Part of the brain responsible for processing data seen and perceived by the eyes:

A

Occipital lobe

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16
Q

Accumulation of blood between the calvarium and dura. It is usually the result of trauma to the side of head that fractures the temporal bone and transects the middle meningeal artery. Often fatal if not surgically treated:

A

Epidural hematoma

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17
Q

Accumulation of blood in the subdural space as a consequence of bleeding from torn bridging veins. Caused by rapid rotation of the head. A history of trauma may or may not be present. To tear the bridging veins requires that the brain be accelerated to a critical rate within the head. Most often fatal.

A

Subdural hematoma

18
Q

A bruise on the cortical surface resulting from head trauma:

A

Cerebral contusion

19
Q

Occur at the branch points of arteries at the base of the brain, e.g., circle of Willis. Risk factors for rupture include hypertension, female sex, atherosclerosis, and collagen deficiency. Rupture is a life-threatening event:

A

Saccular (berry) aneurysm

20
Q

Typically involve large intracranial arteries, vertebral arteries, and the basilar artery. The major complication of in the brain is thrombosis:

A

Atherosclerotic aneurysms

21
Q

This hemorrhage occurs most often (65%) in the basal ganglia-thalamus. Approximately 15% occur in the pons, resulting in loss of consciousness:

A

Hypertensive intracerebral hemorrhage

22
Q

During shock (hypoxia due to poor blood circulation or low blood volume) ischemia & necrosis occurs in the brain in wedge shapes associated with tributary veins:

A

Watershed zones of infarction

23
Q

Physical obstruction to flow of CSF, resulting in dilatation of the ventricular system of the brain:

A

Noncommunicating hydrocephalus

24
Q

Most commonly an acquired abnormality in reabsorption of CSF, most frequently secondary to infection, hemorrhage, or tumor:

A

Communicating hydrocephalus

25
Q

Inflammation of the leptomeninges, the thin membranes enveloping the brain. This compartment contains the CSF and provides a rich culture medium for bacteria. The most common bacterial causes are E. coli, H. influenza, Streptococcus pneumoniae and Neisseria meningitidis. The presence of polymorphonuclear leukocytes (neutrophils) in the CSF is a reliable marker:

A

Leptomeningitis (bacterial meningitis)

26
Q

The most common viral disease in the central nervous system. Almost always self-limited and benign. Patients present with fever and severe headache. It is most commonly caused by enteroviruses such as coxsackievirus, but may be caused by mumps virus, Epstein-Barr virus, or herpes simplex virus.

A

Viral meningitis

27
Q

Occurs when bacteria lodge in capillaries in the brain and elicit an acute inflammatory reaction (cerebritis). Multiplication of organisms and the ensuing inflammatory response can result in the formation of this:

A

Cerebral abscess

28
Q

Inflammation primarily involves the brain parenchyma. Typical symptoms include serious neurologic deficits and impaired consciousness. Viral infections of the brain parenchyma are caused by herpes simplex virus, rabies, poliomyelitis, and arboviruses.

A

Viral encephalitis

29
Q

Most common cause of sporadic cases of viral encephalitis and causes a hemorrhagic, necrotizing encephalitis. It is the most important viral infection of the human nervous system:

A

Herpes simplex virus

30
Q

Transmitted to humans through the saliva of an infected animal. However, there are reports of patients with no known bite exposure. Several of these cases involve people visiting caves inhabited by bats, where inhalation of viral particles in bat feces appears to be the route of infection:

A

Rabies

31
Q

Caused by a small non-enveloped single-stranded RNA virus. The virus infects neurons in the spinal cord and brain stem. Mortality ranges from 5 to 25% with death resulting from respiratory failure:

A

Poliomyelitis

32
Q

A chronic demyelinating disease of the CNS in which there are numerous patches of demyelination throughout the white matter. The disease has a genetic contribution and a possible autoimmune etiology. The plaque is the hallmark of multiple sclerosis. Patients frequently present with blurred vision or loss of vision in one eye. Plaques within the spinal cord cause weakness of one or both legs.

A

Multiple sclerosis

33
Q

An encephalopathy caused by deficiency of thiamine. Patients exhibit lateral rectus palsy, nystagmus, ataxia and mental confusion. Seen most commonly in association with chronic alcoholism:

A

Wernicke syndrome

34
Q

A progressive dementing illness that occurs predominantly in persons over 45 years of age, with the highest incidence in the ninth decade of life. The most common cause of senile dementia among the elderly. Defined pathologically by the presence of numerous senile plaques, neurofibrillary tangles, and neuronal loss:

A

Alzheimer disease

35
Q

A progressive neurodegenerative disease characterized clinically by involuntary movements and cognitive deterioration. Gross examination of the brain reveals marked atrophy of the caudate nucleus. There is a clinically observed phenomenon of “anticipation”, in which future generations show symptoms of disease at a younger age:

A

Huntington disease

36
Q

Characterized pathologically by loss of neurons in the substantia nigra and disruption of specific dopaminergic pathways. Clinically, patients have tremors at rest and muscular rigidity:

A

Parkinson disease

37
Q

A degenerative disease of motor neurons. The most common form of adult onset, progressive motor neuron disease. The principal clinical features of this disease are muscular weakness and atrophy:

A

ALS

38
Q

Tumors of astrocytic origin. They represent the largest and most diverse group of glial cell tumors:

A

Astrocytomas

39
Q

Glial cells that support neurons and can form tumors called glioblastomas:

A

Astrocytes

40
Q

The myelin-producing cells of the central nervous system:

A

Oligodendroglial cells

41
Q

This highly malignant glial cell neoplasm shows numerous mitoses, endothelial cell proliferation, and necrosis. The most likely diagnosis is:

A

Glioblastoma multiforme