Neurology Flashcards

1
Q

A 44-year-old male smoker presents with a 9-year history of recurrent headaches. Headaches occurred twice-monthly initially, always in the early hours of the morning (2 a.m. to 3 a.m.). The headaches have increased to an average of 2 episodes per day. The acute episodes can occur at any time, and last between 2 and 4 hours. He always has a nocturnal event. Attacks are triggered immediately after drinking alcohol or with the smell of strong aftershave or petrol. The pain is excruciating and focused around his right eye. The right eye reddens and tears, the right eyelid droops, and the right nostril runs. He becomes severely agitated during attacks, often pacing the room or rocking back and forth. Physical examinations, lumbar puncture, brain magnetic resonance imaging (including pituitary views), and pituitary function blood tests are normal.

A

Cluster headache

Migrainous features can be seen in cluster headache, including aura symptoms (14% of patients [1] ), ipsilateral photophobia and/or phonophobia (61.2%), and nausea and vomiting (27.8%). [3] During remission periods, patients may report mild pre-headache sensations or shadows in the same location as the cluster headaches. Three percent of patients fail to report autonomic features and agitation during attacks. Continuous background pain has been reported in nearly one third of patients with chronic cluster headache.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

A 37-year-old woman presents with a 12-year history of episodic headaches. She experiences these 4 times a week, typically beginning at the end of a working day. The pain is generalised and described as similar to wearing a tight band around her head. The headaches are bothersome, but not disabling, and she denies any nausea or vomiting. She is slightly sensitive to noise but has no photophobia. Pain during her attacks typically responds to ibuprofen. Examination reveals tenderness of her scalp and both trapezius muscles.

A

Tension headache

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

A 32-year-old woman presents with a 13-year history of 1 to 3 attacks per month of disabling pounding pain over one temple, with nausea and sensitivity to light. She says that her headaches can be triggered by lack of sleep and made worse by physical exertion, and are more common during menstrual bleeding. Untreated, they last for 2 days. On 4 occasions, headaches were preceded by the gradual appearance of a shimmering, zigzag line that enlarged, moved to the peripheral visual field, and then faded away over 45 minutes. Examination is normal.

A

Migraine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

A 40-year-old man complains of a 1-year history of twice-monthly global headache, worse on the left side in the post-auricular region. It comes on gradually and, at its most severe, the vision in his left eye becomes distorted. He often has to stop watching television as the picture becomes “blurry”. His nose becomes blocked, although sometimes he has a “runny nose”. He takes a non-steroidal anti-inflammatory drug (NSAID) that helps a little, but he feels that his head is about to explode at times. When the headache occurs, he needs to go into a dark quiet room and sleep until it resolves. He reports that the problem is “really getting him down”, and he is having difficulties with his employer due to loss of work time.

A

Migraine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

A 56-year-old man presents with a 25-year history of constant headache. The onset was insidious and he is certain that the only time he is headache-free is when he sleeps. He states the headache is generalised and his neck and shoulders are always ‘tight’. He denies any associated autonomic symptoms including eye tearing, nasal congestion, light and sound sensitivity, nausea, or vomiting.

A

Tension headache

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

A 55-year-old woman recently diagnosed with a brain tumour in the left hemisphere has a witnessed seizure event. The seizure is initially recognised when the patient begins staring and is unresponsive to those around her. She seems to be picking at her clothes with her left hand, but the right arm and leg are not moving. After 20 seconds, she displays rapid head-turning and eye deviation to the right, with tonic extension of the right arm and flexion of the left arm. This is quickly followed by tonic extension of the left arm as well, then clonic jerking occurring in both arms synchronously. This jerking gradually slows and stops after about 30 seconds. The patient then becomes quite somnolent, and she appears to be using her arm and leg less on the right than the left.

A

generalised epilepsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

An 18-year-old girl presents with several episodes of confusion over the past several months. Typically, she experiences a warning signal, which she describes as a rising sensation within her abdomen that travels upwards through her chest. She is usually unaware for a few minutes, but others have told her that she smacks her lips, picks at her clothing, and is unable to speak during these episodes. After the event she feels tired, has a headache, and prefers to lie down. She notes that her memory has not been as good as it was in the past, and her school grades have declined. Her past medical history is notable for several febrile seizures as a young child, although she was not treated for seizures at that time. An aunt was diagnosed with seizures many years ago.

A

focal seizures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

A middle-aged woman presents with a complaint of frequent (once or twice daily for 3 weeks), brief (lasting several seconds) episodes of intense, sharp left-sided jaw pain. She has experienced these attacks for several years, but they had previously been relatively rare (1 episode daily for several consecutive days followed by months with no attacks). She says that episodes are sometimes brought on by eating but can occur without an apparent stimulus. The patient states that even though the pain is brief, she lives in fear of repeat flares.

A

Trigeminal Neuralgia

Maxillary/mandibular (V2/V3) distribution symptoms occur in the majority of patients. This can present as sharp pain running from the mouth to the jaw (commonly mistaken for dental pain) or less commonly as pain from the upper lip to the orbit. Symptoms in an exclusively ophthalmia (V1) distribution are the least common, and patients typically refer to the pain as headache.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

A 40 year old woman presents with a 7 month history of continuous, but fluctuating, left facial pain. It is usually dull but there can be piercing pain in the cheek. It is aggravated by chewing and diminished by relaxing or massaging facial muscles. The dentist cannot find a cause.

A

Facial arthromyalgia (TMJ syndrome)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

An 80 year old man arrives in A&E distressed. He has had excruciating pain and tenderness over the left side of his forehead since an episode of shingles 3 months previously.

A

Postherpetic neuralgia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

A 32 year old woman presents with a 3 year history of constant dull L facial pain. There are no aggravating or relieving factors and she has gained no benefit from tricyclics, gabapentin or opiate analgesics. The pain is dominating her life, preventing work, and making her depressed. Her GP, dentist and an ENT surgeon have not found a cause. O/E normal

A

Atypical facial pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

A 65-year-old woman presents with a chief complaint of dizziness. She describes it as a sudden and severe spinning sensation precipitated by rolling over in bed onto her right side. Symptoms typically last <30 seconds. They have occurred nightly over the last month and occasionally during the day when she tilts her head back to look upwards. She describes no precipitating event prior to onset and no associated hearing loss, tinnitus, or other neurological symptoms. Otological and neurological examinations are normal except for the Dix-Hallpike manoeuvre, which is negative on the left but strongly positive on the right side.

A

Benign paroxysmal positional vertigo

BPPV can occur as a result of a closed-head injury or vestibular neuronitis, and it can also be associated with Meniere’s disease or migraine. Most patients give the classic description of a short-lived vertigo sensation following rolling over in bed. However, many patients may not sense an actual turning sensation and may use other dizziness descriptors to describe their sensation. Because of the frightening intensity of the sensations, patients often report that the spells last for 5 or 10 minutes when in reality they typically last for no more than 20 seconds.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

A 40-year-old woman presents with a 1-year history of recurrent episodes of vertigo. The vertigo spells are described as a sensation of the room spinning that lasts from 20 minutes to a few hours and may be associated with nausea and vomiting. The spells are incapacitating and are accompanied by dizziness, vertigo, and disequilibrium, which may last for days. No loss of consciousness is reported. The patient also reports aural fullness, tinnitus, and hearing loss in the right ear that is more pronounced around the time of her vertigo spells. Physical examination of the head and neck is normal. A horizontal nystagmus is noted. She is unable to maintain her position during Romberg’s testing or the Fukuda stepping test. She turns towards the right side and she is unable to walk tandem. Her cerebellar function tests are normal.

A

Meniere’s Disease

Patients may present with any combination of hearing loss, tinnitus, vertigo, or aural fullness.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

A 69-year-old man presents with a 1-year history of mild slowness and loss of dexterity. His handwriting has become smaller, and his wife feels his face is less expressive and his voice softer. Over the last few months he has developed a subtle tremor in the right hand, noted while watching television. His symptoms developed insidiously but have mildly progressed. He has no other medical history, but he has noted some mild depression and constipation over the last 2 years. His examination demonstrates hypophonia, masked facies, decreased blink rate, micrographia, and mild right-sided bradykinesia and rigidity. An intermittent right upper extremity resting tremor is noted while he is walking. The rest of his examination and a brain MRI are normal.

A

Parkinson’s

PD can present in myriad ways. The cardinal features of resting tremor, bradykinesia, rigidity, and postural instability can occur in various combinations and sequences during the course of the disease. The signs and symptoms are typically asymmetrical. Bradykinesia and rigidity often present in subtle fashion early in the disease course. For example, reduced arm swing, shuffled gait, softened voice, decreased blink rate, decreased facial expressivity, and reduced spontaneous movement are all signs of parkinsonism. The non-motor symptoms of PD, such as depression, fatigue, autonomic dysfunction (constipation, incontinence, dysphagia), and sleep disturbance may even precede the evolution of motor symptoms. Given their non-specificity, however, their relationship to PD is only made after motor symptoms/signs have been identified.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

A 67-year-old man with a prior history of hypertension, diabetes, hyperlipidaemia, and a 50 pack-year smoking history noted rapid onset of right-sided weakness and subjective feeling of decreased sensation on his right side. His family reported that he seemed to have difficulty forming sentences. Symptoms were maximal within a minute and began to spontaneously abate 5 minutes later. By arrival in the emergency department 30 minutes after onset, his clinical deficits had largely resolved with the exception of a subtle weakness of his right hand. Forty minutes after presentation, all of his symptoms were completely resolved.

A

TIA

Presentation of TIA is dictated by the region of brain supplied by the obstructed vessel. Unilateral weakness or sensory deficits may result from ischaemia in the carotid distribution. This presentation represents 67% of all TIAs. [5] Aphasia from ischaemia of Wernicke’s or Broca’s area occurs in 13% of TIAs. [5] Posterior cerebral artery occlusion may give homonymous hemianopsia, whereas thrombus in the retinal artery leads to amaurosis fugax. Posterior circulation ischaemia may lead to symptoms of ataxia, vertigo, incoordination, cranial nerve deficits, or syncope, and such symptoms are described in 17% of new TIAs. [5] Isolated dizziness is rarely a symptom of TIA or stroke. [6] Lacunar symptoms tend to give isolated sensory or isolated motor deficits but also a number of less common symptom complexes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

A 70-year-old right-handed man is discovered by a family member to have difficulty speaking and comprehending spoken language, and an inability to raise his right arm. He was last known to be fully functional 1 hour ago when the family member spoke to him by phone. There is a history of treated hypertension and diabetes.

A

ischaemic stroke

The presenting symptoms of stroke vary by cerebral location. Most common symptoms are partial or total loss of strength in upper and/or lower extremities, expressive and/or receptive language dysfunction, sensory loss in upper and/or lower extremities, visual field loss, slurred speech, or difficulty with fine motor co-ordination and gait. In most cases the symptoms appear rapidly, over seconds or minutes, and may be preceded by one or more transient ischaemic attacks. There are no symptoms or signs that reliably distinguish between ischaemic and haemorrhagic stroke. The acute onset of neurological symptoms referable to the brain territory of a cerebral artery strongly suggests ischaemic stroke, but mimicking conditions such as intracerebral haemorrhage, focal seizure, and complicated migraine need to be considered and excluded.

17
Q

A 70-year-old man with a history of chronic hypertension and atrial fibrillation is witnessed by a family member to have nausea, vomiting, and right-sided weakness as well as difficulty speaking and comprehending language. The symptoms started with only mild slurred speech before progressing over several minutes to severe aphasia and right arm paralysis. The patient is taking warfarin.

A

haemorrhagic stroke (intracerebral hg)

Headache occasionally accompanies intracerebral haemorrhage, but its absence does not rule out the diagnosis.

18
Q

A 53-year-old black woman complains of a sudden, excruciating headache while sitting at work. The headache is diffuse, intense, and accompanied by nausea and vomiting. She describes the headache as the worst headache of her life. She loses consciousness following onset of the headache and is on the floor for less than 1 minute. She is being treated for hypertension and is a smoker. On examination she has a normal mental state, meningismus, bilateral subhyaloid haemorrhages, and right third cranial nerve palsy. There are no sensory deficits or weakness. Brain computed tomography (CT) reveals diffuse subarachnoid blood in basal cisterns and sulci.

A

SAH

An atypical history of SAH includes less severe headaches, headaches accompanied by vomiting and low-grade fever, and prominent neck pain. Around 10% to 43% of patients experience a sentinel headache during the 3 months prior to SAH. [2] Some of these headaches are caused by minor leaks from the aneurysm, which CT is unreliable in detecting. [3] Patients who experience sentinel headache might have an increased risk of rebleeding.

19
Q

A 48-year-old insurance salesman presents with a 25-year history of back pain. He developed severe back pain while stacking shelves at the local supermarket at age 23. The pain resolved after 10 days of bed-rest, followed by 3 months of physiotherapy. He has had multiple episodes of back pain occurring at increasing regularity over the years and, in the past 10 years, has changed his occupation to salesperson. Currently, he has back pain measuring 8 out of 10 on a visual analogue scale and bilateral leg pain. The back pain is exacerbated by flexion, and the leg pain is reproduced by a straight leg raise of 70 degrees. He has numbness of both feet in the L5 dermatome; motor and reflexes are normal.

A

Disc degeneration

Progression of disc degeneration may lead to additional painful manifestations, including loss of disc height and facet joint arthrosis, disc herniation and nerve root irritation, [1] and hypertrophic changes resulting in spinal stenosis. [2] As a result, patients with degenerative disc disease may present with a variety of symptoms that range from mild localised tenderness to severe excruciating radicular pain and lower extremity symptoms.

20
Q

A 65-year-old retired builder has had lower back pain for 3 years. For the past 12 months he has been experiencing bilateral leg pain and a sense of heaviness in the legs when he is walking. The pain is relieved by bending over or sitting down. Over the past few months the distance he is able to walk has become progressively shorter and he has assumed a stooped posture. Physical examination is essentially unremarkable. Distal pulses are palpable and there is no appreciable weakness or muscle atrophy in the legs, or findings of hip or knee pathology.

A

Spinal stenosis

Patients with a congenitally narrowed lumbar spinal canal present at a younger age. Rarely, patients present with symptoms of significant leg muscle weakness and atrophy or sphincter dysfunction, but this is unusual in the absence of substantial low back or leg pain. Symptoms of leg pain, numbness, and tingling upon standing or ambulation may be unilateral but more often are bilateral. Radiculopathy, characterised by pain radiating in a specific dermatomal pattern rather than causing symptoms of neurogenic claudication, is usually the result of stenosis in the lateral recesses and the neural foramina.

21
Q

A 28-year-old man presented to the emergency department for low back pain and numbness in both lower extremities. Two days earlier, he had sharp, shooting pains in the back and buttocks after moving boxes. The pain was relieved with hydrocodone with acetaminophen. However, on the morning of presentation, the patient awoke with numbness in both lower extremities and had left leg weakness so severe that the patient was unable to stand or walk without support. The patient described the pain as mild while he was supine and worse when he sat or stood. The patient reported some urinary hesitancy, dribbling of urine, and constipation. He did have morning erections. The patient reported that he had had an industrial injury five years before that resulted in a herniated lumbar disk and subsequent laminectomy; he had been doing well since then until the time of presentation.

A

Cauda equina syndrome

22
Q

A young man is brought to the emergency department after being involved in a high-speed motor vehicle accident. He was an unrestrained driver, and no airbags were deployed. He has multiple areas of abrasions, lacerations, and ecchymosis on his scalp and face. On neurological examination, he does not open his eyes to painful stimuli; he is intubated, and he withdraws his left side to pain. His right side is plegic. His right pupil is 3 mm and reactive to light and his left pupil is 8 mm and non-reactive.

A

subdural haematoma

23
Q

A 75-year-old man presents with problems walking that have developed over the previous 2 years, consisting of slow gait, imbalance (especially on turning), short stride length, and gait initiation failure. He reports urinary frequency, occasional urge incontinence, and some memory loss. On examination, his symptoms are symmetrical and much more prominent in the lower half of the body, with relative sparing of hand function, and normal facial expressiveness. He has previously been diagnosed with Parkinson’s disease; however, therapy with levodopa has not improved his symptoms.

A

normal pressure hydrocephalus

Faecal incontinence is a feature of advanced disease and is rare.

24
Q

A 29-year-old woman presents with a 3-month history of worsening headaches and increasing visual loss. She describes occasional episodes of bilateral visual greyouts lasting 20 seconds that may be precipitated by bending forwards or standing. Over the last 2 weeks she has often heard a ‘whooshing’ sound, synchronous with her pulse, that is more noticeable when she is about to go to sleep. Her visual acuity is 20/30 (6/9 metres) in each eye. Fundus examination shows bilateral optic disc swelling, and Humphrey automated perimetry shows enlargement of the blind spot and scattered abnormal test locations. Magnetic resonance imaging shows a partially empty sella, and a magnetic resonance venogram shows no evidence of a thrombosis but does demonstrate bilateral transverse sinus venous stenoses. Lumbar puncture opening pressure is 280 mm H2O.

A

Idiopathic intracranial hypertension

25
Q

An older man with a longstanding history of atrial fibrillation on anticoagulation with warfarin is brought into the emergency department by his carer, who states his concern about the patient’s confusion at home. The carer describes frequent falls over the last several months and says that the patient is dropping utensils from his right hand. On neurological examination, his pupils are equal, round, and reactive to light. He has a right-sided pronator drift and is weaker on his right side than on his left. His mental status testing reveals poor concentration and attention, and impaired short- and long-term recall and registration.

A

Subdural haematoma

26
Q

A 20-year-old woman with no significant past medical history presents with lower back pain and bilateral foot and hand tingling. Her symptoms rapidly progress over 4 days to include lower extremity weakness to the point that she is unable to mobilise her lower extremities. She reports coryzal symptoms 2 weeks ago. On examination, she has 0/5 power in her lower extremity with areflexia, but despite the paraesthesias she does not have sensory deficits. Her aminotransferases are elevated, and lumbar puncture reveals mildly elevated protein with no cells and normal glucose. She weighs 70 kg and her admission vital capacity is 1300 mL, maximum inspiratory pressure is -30 cmH₂O, and maximum expiratory pressure is 35 cmH₂O.

A

Guillian Barre Syndrome

27
Q

A 67-year-old man with a medical history of pancreatoduodenectomy (Whipple procedure) in September 2015 due to a pancreatic cancer was admitted to our department of neurology 1 year later with a progressively disturbed gait. He reported weakness and numbness of both legs. Clinical examination revealed a spastic sensomotoric tetraparesis with ataxia and bladder dysfunction. MRI showed longitudinal myelopathy exactly limited to the posterior tracts (fasciculus gracilis and fasciculus cuneatus) indicating a metabolic origin

A

subacute combined degeneration of the spinal cord