The Neurological Examination and Diagnostic Tests Flashcards
- An 85-year-old man is being evaluated for gait difficulties. On examination it is found that joint proprioception is absent in his toes. People with impaired position sense will usually fall if they stand with their feet together and do which of the following?
a. Flex the neck
b. Extend their arms in front of them
c. Flex the knees
d. Turn the head
e. Close their eyes
E
(Victor, pp 123, 165–166.) Standing with the feet together and the eyes closed is the Romberg test. The person with poor position sense needs visual cues to remain standing. This test was intro- duced as a helpful way to check for deficits associated with tabes dorsalis, a form of neurosyphilis. In tabes dorsalis, the dorsal columns of the spinal cord are damaged. These dorsal or posterior columns carry the nerve fibers that transmit vibration and position sense to the brain. With the wide- spread use of penicillin, tabes dorsalis has become rare in industrialized nations, and impaired position sense is much more likely to be a consequence of diabetes mellitus or alcoholism. In both of these conditions, the impaired position sense is much more likely to be a consequence of damage to nerves in the limbs than of damage to the posterior columns of the spinal cord. In performing the test, it is important to remember that even normal people will tend to sway slightly more when their eyes are closed, and that those with loss of cerebellar function will also sway more with loss of visual cues.
- An 81-year-old woman with a history of type II diabetes mellitus and atrial fibrillation presents with right body weakness and slurred speech. She realized that there was a problem on awakening in the morning, and her husband called EMS, who brought her to the emergency room. There are no word-finding difficulties, dysesthesia, or headaches. She is taking warfarin. Physical exam findings include blood pressure of 210/95 and irregularly irregular heartbeat. There is left side neglect with slurred speech. There is a corticospinal pattern of weakness of the right body, with the face and upper extremity worse than the lower extremity. Routine chemistries and cell counts are normal. Her INR is 1.7. A head CT reveals a large left-sided subdural hematoma. The intracranial material appearing most dense on computed tomography (CT) of the head is which of the following?
a. Blood clot
b. White matter
c. Gray matter
d. Cerebrospinal fluid (CSF)
e. Pia mater
A
(Osborn, pp 158–159.) Computed tomographic scanning measures the density of intracranial as well as extracranial structures. Bone appears much denser than blood, but blood is obvious on the unenhanced (precontrast) CT scan precisely because it is much denser than white matter, gray matter, and CSF. The resolution of the CT scan is generally not sufficient to differentiate the pia mater from the gray matter on which it lies. Other meningeal structures, such as the dura mater, may appear denser than brain, especially if there is some calcification in the membranes.
- A 21-year-old woman presents with right arm loss of sensation that has been progressive over a few days. Her physician is concerned that this might be some type of demylinating disorder. A relatively small plaque of demyelination, should be evident on which of the following?
a. T1-weighted MRI
b. T2-weighted MRI
c. Precontrast CT
d. Diffusion-weighted MRI
e. PET
B
(Osborn, p 757.) Magnetic resonance imaging looks primarily at the water content of tissues, but it can be customized to look at specific properties of tissues. A variety of methods are available for affecting the information produced by and analyzing the information generated by MRI. The T1-weighted image enhanced by gadolinium contrast agent is useful for identifying inflammation and other causes of fluid extravasation into the brain. The T2-weighted image is not specific for demyelination, but it is useful in following changes in plaques of demyelination, an application that has been used in studies of agents useful in the management of multiple sclerosis. Magnetization transfer and other more complex tech- niques have been developed to look at demyelination specifically, but they are not generally available. The diffusion–weighted image technique looks at the diffusion coefficients of water molecules in tissues and is proving useful in studies of acute stroke. The CT scan cannot readily distinguish between tissues of similar densities. Positron emission tomography is primarily a research tool that is useful in determining what materials are used or are unavailable for use in specific parts of the brain.
A 62-year-old right-handed man has “involuntary twitches” of his left hand. He first noticed between 6 months and 1 year ago that when he is at rest, his left hand shakes. He can stop the shaking by looking at his hand and concentrating. The shaking does not impair his activities in any way. He has no trouble holding a glass of water. There is no tremor in his right hand and the lower extremities are not affected. He has had no trouble walking. There have been no behavioral or language changes. On examination, a left hand tremor is evident when he is distracted. Handwriting is mildly tremulous. He is very mildly bradykinetic on the left.
- The most likely exam finding would be which of the following?
a. Upper motor neuron pattern of weakness on the left
b. Lower motor neuron pattern of weakness on the left
c. Bilateral upper motor neuron pattern of weakness
d. Mild cogwheel rigidity on the left only with distraction
e. Bilateral severe cogwheel rigidity
D
(Greenberg, 5/e, pp 241–243.) This patient gives a typical history for early Parkinson’s disease. The classic triad is asymmetric resting tremor, rigidity, and bradykinesia. The rigidity is generally severe later, not early in the disease. Parkinson’s disease is not characterized by weakness.
A 62-year-old right-handed man has “involuntary twitches” of his left hand. He first noticed between 6 months and 1 year ago that when he is at rest, his left hand shakes. He can stop the shaking by looking at his hand and concentrating. The shaking does not impair his activities in any way. He has no trouble holding a glass of water. There is no tremor in his right hand and the lower extremities are not affected. He has had no trouble walking. There have been no behavioral or language changes. On examination, a left hand tremor is evident when he is distracted. Handwriting is mildly tremulous. He is very mildly bradykinetic on the left.
- Tremor in the hands that is most obvious when the patient is awake and trying to perform an action is most likely due to disease in which of the following structures?
a. Thalamus
b. Cerebellum
c. Substantia nigra
d. Spinal cord
e. Internal capsule
B
( Victor, p 90.) Intention or kinetic tremors are most characteristic of damage to the cerebellum. Kinetic tremors of the hand or arms are most common with disease of the cerebellar hemispheres, but they may also develop with damage to the spinocerebellar tracts of the spinal cord. Damage to the substantia nigra, such as that occurring in Parkinson’s disease, produces a resting tremor that abates when the patient moves the involved limb intentionally. Damage to the thalamus is more likely to produce a sensory disturbance. Tremors may develop with spinal cord damage, but they do not follow a typical pattern and do not suggest a spinal cord origin.
A 62-year-old right-handed man has “involuntary twitches” of his left hand. He first noticed between 6 months and 1 year ago that when he is at rest, his left hand shakes. He can stop the shaking by looking at his hand and concentrating. The shaking does not impair his activities in any way. He has no trouble holding a glass of water. There is no tremor in his right hand and the lower extremities are not affected. He has had no trouble walking. There have been no behavioral or language changes. On examination, a left hand tremor is evident when he is distracted. Handwriting is mildly tremulous. He is very mildly bradykinetic on the left.
- In the person with Parkinson’s disease, the tremor that is evident when a limb is at rest changes in what way when the patient falls asleep?
a. It becomes more rapid
b. Its amplitude increases
c. It generalizes to limbs that were uninvolved when the patient was awake
d. It disappears
e. It transforms into choreiform movements
D
( Hauser, p 27.) Patients with Parkinson’s disease often have a characteristic pill-rolling tremor of the hand while they are awake. The tremors associated with Parkinson’s disease are worse when the patient is at rest and not moving the affected limb. Paradoxically, this resting tremor ceases when relaxation progresses to sleep. In fact, most tremors and other types of movement disorders caused by disease of the caudate, putamen, and globus pallidus (i.e., the basal ganglia) and of the substantia nigra remit during sleep. Choreiform movements are jumping or dancelike movements and occur with Wilson’s disease (hepatolenticular degenera- tion) and Huntington’s disease, a hereditary degenerative disease of the basal ganglia.
- A 25-year-old woman with a history of epilepsy presents to the emergency room with impaired attention and unsteadiness of gait. Her phenytoin level is 37. She has white blood cells in her urine and has a mildly elevated TSH. Examination of the eyes would be most likely to show which of the following?
a. Weakness of abduction of the left eye
b. Lateral beating movements of the eyes
c. Impaired convergence
d. Papilledema
e. Impaired upward gaze
B
(Rowland, p 823.) Most rhythmic to-and-fro movements of the eyes are called nystagmus. Nystagmus has a fast component in one direction and a slow component in the opposite direction. Nystagmus with a fast component to the right is called right-beating nystagmus. Phenytoin (Dilantin) may evoke nystagmus at levels of 20 to 30 mg/dL. The eye movements typically appear as a laterally beating nystagmus on gaze to either side; this type of nystagmus is called gaze-evoked. If the patient has nystag- mus on looking directly forward, he or she is said to have nystagmus in the position of primary gaze. Therapeutic levels for phenytoin are usually 10 to 20 mg/dL, and some patients develop asymptomatic nystagmus even within that range. Ataxia, dysarthria, impaired judgement, and lethargy may also occur at toxic levels of phenytoin. Many other drugs also evoke nystagmus. Weakness of abduction of the left eye, or abducens palsy, is due either to injury to the sixth cranial nerve or to increased intracranial pressure. Impaired convergence can occur normally with age or may be a sign of injury to the midbrain. Papilledema is a sign of increased intracranial pressure. Impaired upward gaze may occur in many conditions, but would not be expected to occur with a toxic phenytoin level.
- A 75-year-old generally healthy man has noticed worsening problems maneuvering over the past 4 months. He has particular trouble getting out of low seats and off toilets. He most likely has which of the following?
a. Poor fine finger movements
b. Poor rapid alternating movements
c. Distal muscle weakness
d. Proximal muscle weakness
e. Gait apraxia
D
( Braunwald, p 2522.) With primary muscle diseases, such as polymyositis, weakness usually develops in proximal muscle groups much more than in distal groups. This means that weakness will be most obvious in the hip girdle and shoulder girdle muscles. The hip girdle is usually affected before the shoulder girdle. To get out of a low seat, the affected person may need to pull him- or herself up using both arms. Per- sons with more generalized weakness or problems with coordination are less likely to report problems with standing from a seated position. Poor rapid alternating movements and poor fine finger movements usually develop with impaired coordination, such as that due to cerebellar damage. With severe weakness in the limbs, patients will do poorly on these tests of function as well. With proximal muscle weakness, the affected person will usually perform relatively well on these tests of distal limb coordination.
- A 50-year-old woman is being examined for hearing loss. A vibrating tuning fork is applied to the center of her forehead. This helps to establish which ear
a. Has the wider range of frequency perception
b. Has the larger external auditory meatus
c. Has infection of the external ear canal
d. Has the longer eustachian tube
e. Has conductive or sensorineural hearing loss
E (Victor,p306.)Thevibrationsfromatuningforkplaced on top of the head are transmitted through the skull to both ears. Bone con- duction of sound through the skull should be equal in both ears. With sensorineural hearing loss, the patient will hear the midline fork more loudly in the unaffected ear. Sensorineural hearing loss is the deafness that develops with injury to the receptor cells in the cochlea or to the cochlear division of the auditory nerve. In conductive hearing loss, the vibrations of the tuning fork are perceived as louder in the affected ear. With this type of hearing loss, the injury is in the system of membranes and ossicles designed to focus the sound on the cochlea. Impairment of the conductive system causes the vibrations of the tuning fork to be transmitted to the cochlea directly through the skull. Much like a person with cotton stuffed into the external auditory meati, the patient with the conductive hearing loss has impaired perception of sound coming from around him or her but an enhanced perception of his or her own voice. This type of tuning fork test is called the Weber test.
- A 67-year-old woman says that she is having problems with dizziness. A more careful history reveals that she has an abnormal sensation of move¬ment intermittently. Which of the following tests would be most helpful in determining the cause of episodic vertigo? a. CSF b. C-spine MRI c. Visual evoked response (VER) d. Electronystagmography (ENG) e. Electroencephalography (EEG)
D (Bradley, pp 733–736.) ENG is used primarily to characterize nystagmus and disturbances of eye movements that involve rel- atively fast eye movements. Abnormal patterns of eye movement may help localize disease in the central or peripheral nervous system in patients with vertigo. The retina is negatively charged in comparison with the cornea, which creates a dipole that is monitored during ENG studies by electrodes placed on the skin about the eyes. Movement of the most posterior elements of the retina toward an electrode is registered as a negative voltage change at that electrode. Damage to the pons may produce characteristic conjugate deviations of the eyes. The conjugate eye movements are rhythmic and directed downward, but they lack the rapid component characteristic of nystagmus. This type of abnormal eye movement is called ocular bobbing. A lesion at the cervicomedullary junction, such as a meningioma at the foramen magnum, will produce a down-beating nystagmus with both eyes rhythmically deviating downward, with the rapid component of this nys- tagmus directed downward as well. Cervicomedullary refers to the cervical spinal cord and the medulla oblongata. Damage to the midbrain, thalamus, or hypothalamus may disturb eye movements, but down-beating nystagmus would not ordinarily develop with damage to these structures.
- A 67-year-old woman says that she is having problems with dizziness. A more careful history reveals that she has an abnormal sensation of move¬ment intermittently. This patient develops increased sensitivity to sound in her left ear, and a brain MRI reveals a posterior fossa mass. This symptom may develop in one ear with damage to the ipsilateral cranial nerve a. V b. VII c. VIII d. IX e. X
B (Victor, pp 1451–1452.) The facial nerve innervates the stapedius muscle of the middle ear. With paralysis of this muscle, undamped transmission of acoustic signals across the stapedius bone of the middle ear produces hyperacusis. Hyperacusis is an indication that the damage to the facial nerve is close to its origin from the brainstem, because the nerve to the stapedius muscle is one of the first branches of the facial nerve. The tensor tympani is controlled by the motor fibers in the fifth cranial nerve. With damage to this nerve, the tympanic membrane has some inappropriate slack, but the patient does not usually comment on increased sensitivity to sound in the affected ear.
- A 42-year-old woman is being evaluated for gait difficulties. On examination, it is found that her ability to walk along a straight line touching the heel of one foot to the toe of the other is impaired. This finding is most common with which of the following? a. Cerebellar dysfunction b. Parietal lobe damage c. Temporal lobe damage d. Ocular motor disturbances e. Dysesthesias in the feet
A (Greenberg, 5/e, p 104.) Walking along a straight line with the heel of one foot touching the toe of the other foot is called heel-to- toe walking, or tandem gait. It is a routine test for ethanol intoxication because alcohol exposure impairs the coordination of gait as governed by the cerebellum. Tandem gait will be abnormal with many other problems, including weakness, poor position sense, vertigo, and leg tremors, but such abnormality in the absence of these other problems suggests a cerebellar basis for the problem.
- A 55-year-old woman is being examined. The clinician notices the presence of fine twitching movements beneath the surface of the tongue and wasting of one side of the tongue. This finding suggests damage to cranial nerve a. V b. VII c. IX d. X e. XII
E (Greenberg, 5/e, p 360.) The hypoglossal nerve innervates the tongue. The fine movements noted under the surface of the tongue with injury to the hypoglossal nerve are called fasciculations and are an indication of denervation. They are presumed to occur through hypersensi- tivity to acetylcholine acting at the denervated neuromuscular junction. Atrophy and fasciculations are likely to occur together and are highly suggestive of denervation of the tongue. This is most often seen with brainstem disease, such as stroke or bulbar amyotrophic lateral sclerosis (ALS), or with transection of the hypoglossal nerve.
- A 46-year-old longshoreman complains of lower back pain radiating down the posterior aspect of his left leg, and paresthesias in the lateral aspect of his left foot. This has been present for 6 months. Strength and bowel and bladder function have been normal. Examination would be most likely to show which of the following? a. Left Babinski sign b. Loss of pinprick sensation over the webspace between the first and second digits of the left foot c. Hyperreflexia at the left knee jerk d. Hyporeflexia in the left Achilles tendon reflexe. Decreased rectal tone
D ( Victor, pp 213–215.) This patient has a history most consistent with a herniated lumbar disk. The most common locations for lumbar disk herniation are between the fifth lumbar and first sacral vertebrae (producing S1 nerve root compression) and between the fourth and fifth lumbar vertebrae (producing L5 root compression). S1 nerve root compression, or radiculopathy, is associated with pain in the lower back or buttock region, often radiating down the posterior thigh and calf to the lateral and plantar surfaces of the foot and affecting the fourth and fifth digits of the foot. Motor function of the foot and toe flexors, toe abductors, and hamstring muscles may be impaired but more often is not. Bowel and bladder function are usually preserved. The loss of the ankle jerk, or Achilles tendon reflex, is often the only objective sign of S1 radiculopathy. Deep tendon reflexes such as the ankle jerk are diminished or lost when there is damage to the sensory fibers from the tendon stretch organs. A Babinski sign is an indication of upper motor neuron damage, which is not expected in this case with preserved autonomic and motor function. Loss of pinprick sensation over the web space between first and second toes is found in association with injury to the fifth lumbar nerve root or to the peroneal nerve. Hyperreflexia of the knee jerk is another sign of an upper motor neuron lesion and would not be expected in this case. Straight-leg raising (Lasègue maneuver) is used to determine whether symptoms are due to nerve root compression by stretching the nerve root. With compression, lifting the leg passively may be limited to between 20 and 30°. This test may be positive on the contralateral side (crossed straight-leg raising sign), but it is usually more prominent on the affected side.
- A 28-year-old graduate student presents with confusion and mild right hemiparesis developing over the course of an evening. His girlfriend relates that he has been complaining of severe headaches each morning for the past 2 weeks. While being evaluated in the emergency room, he has a generalized tonic—clonic seizure. When examined 2 h later, he is lethargic and unable to recall recent events, has difficulty naming, and has a right pronator drift. There is mild weakness of abduction of the eyes bilaterally. Funduscopic examination might be expected to show which of the following? a. Pigmentary degeneration of the retina b. Hollenhorst plaques c. Retinal venous pulsations d. Blurring of the margins of the optic disc e. Pallor of the optic disc
D (Victor, pp 258–260, 684–686.) The presentation with subacute onset of morning headaches culminating in confusion, right hemiparesis, and seizure in a young person suggests an expanding mass lesion, most likely a tumor. The weakness of eye abduction bilaterally is what may be referred to as a false localizing sign. Although this suggests injury to the sixth cranial nerves bilaterally, the injury is not restricted to the sixth cranial nerve. The increase in intracranial pressure (ICP) from the mass causes stretching of the sixth-nerve fibers, which consequently leads to their dysfunction. Diplopia may be appreciated only on lateral gaze, which requires full function of the sixth nerve. Funduscopic exam in such a case would most likely reflect changes of increased ICP. The first sign of this is usually blurring of the margins of the optic disc and elevation of the disc due to swelling. Changes in the optic disc—the area in which all the nerve fibers from the retina come together and exit as the optic nerve— occur with problems other than increased ICP (such as optic neuritis), but blurring of the margins should be routinely considered a sign of increased ICP.This is especially true if the appearance of the disch as changed in association with the development of headache, obtundation, and vomiting. Pigmentary degeneration of the retina may occur with some infections, such as congenital toxoplasmosis or cytomegalovirus, or as part of a hereditary metabolic disorder, as in retinitis pigmentosa. Hollenhorst plaques are cholesterol and calcific deposits seen in the retinal arterioles in the setting of at her oembolism to the eye, along with visual loss. Retinal venous pulsations are typically not present when there is increased ICP, although they may also be absent in up to 15% of normal individuals.
- Taking a normal, awake person who is lying supine with head slightly elevated (30°) and irrigating one external auditory meatus with warm water will induce a. Tonic deviation of the eyes toward the ear that is stimulated b. Nystagmus in both eyes toward the ear that is stimulated c. Tonic deviation of the ipsilateral eye toward the ear that is stimulated d. Nystagmus in both eyes away from the ear that is stimulated e. Tonic deviation of both eyes away from the ear that is stimulated
B (Victor,p319.)Caloric stimulation of th ear drives the endolymphatic fluid in the inner ear up or down, depending on whether warm or cold water is used. By tilting the head of a supine patient up 30° from the horizontal, the semicircular canal responsible for detecting hori- zontal head movements is placed in a vertical plane and caloric stimulation drives the endolymph in that canal more effectively than it will the endolymph in the other semicircular canals. The vestibular organ exposed to warm water sends impulses to the brainstem that indicate that the head is moving to the side that is being warmed. The eyes deviate to the opposite side to maintain fixation on their targets, but the eye movement actually breaks fixation. A reflex nystagmus toward the ear that is being stimulated develops as the brain tries to establish refixation while the vestibular signals repeatedly prompt deviation of the eyes contralateral to the warm stimulus.
- A 33-year-old woman has the acute onset of right orbital pain after a ten¬nis match. The following morning, her 10-year-old son comments that her right eye looks funny. On examination, she has a mild right ptosis and anisocoria. The right pupil is 2 mm smaller than the left, but both react normally to direct light stimulation. Visual acuity, visual fields, and eye movements are normal. The site of injury is due to interruption of fibers from which of the following structures? a. Optic tract b. Optic chiasm c. Cranial nerve III d. T1 nerve root e. Superior cervical ganglion
E ( Victor, p 319. Kandel, p 963.) The presence of ptosis and miosis indicate oculosympathetic palsy, or Horner syndrome. This indicates injury to the sympathetic supply to the eye. This pathway begins in the hypothalamus, travels down through the lateral aspect of the brain- stem, synapses in the intermediolateral cell column of the spinal cord, exits the spinal cord at the level of T1, and synapses again in the superior cervical ganglion. From there, postganglionic fibers travel along the surface of the common carotid and internal carotid artery until branches leave along the ophthalmic artery to the eye. Fibers of the sympathetic nervous system, which are destined to serve the sudomotor function of the forehead, travel with the external carotid artery. Thus, diseases affecting the internal carotid artery and the overlying sympathetic plexus do not produce anhidrosis, the third element of Horner syndrome. In this case, the occurrence of painful Horner syndrome acutely after vigorous activity is virtually diagnostic of carotid artery dissection. Dissections may occur more frequently in migraineurs. The preservation of visual fields and acuity excludes significant disease of the optic tract and chiasm, which also would not be expected to cause ptosis. Lesions of cranial nerve III (CN 3) do cause ptosis, but they would also be expected to cause ipsilateral mydriasis, or pupillary enlargement, not miosis. The degree of ptosis is usually much more severe in third-nerve palsy than in Horner syndrome; this is because CN 3 supplies the levator palpebrae, the primary levator of the lid, whereas the sympathetics supply Müller’s muscle, which plays an accessory role. The sympathetic pathway does exit the spinal cord at T1, but injury at this location would not cause orbital pain, which is typical of carotid arterial dissection.