paraperesis
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Clinical features of Paraperesis
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MULTIPLE SCLEROSIS
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Patients with MS may present with many other
manifestations, including the following:
Aphasia or dysphasia (occurs very rarely)
Seizures (5% of patients with MS)
Other paroxysmal symptoms (eg, ataxia,
akinesia, paresthesias, pruritus) Significant motor complaints without sensory
deficits
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Fatigue
Fatigue is one of the most common symptom
of MS, reported by at least 75% of patientswith the disease.
An estimated 50-60% of persons with MS
describe fatigue as one of their mostbothersome symptoms, and it is a majorreason for unemployment among MSpatients.
Rule out comorbid medical conditions, such as infections, anemia, vitamindeficiencies (eg, vitamin B12, folic acid, vitamin D deficiency) or thyroid
disease, before attributing fatigue to MS.
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Optic neuritis
Optic neuritis can be the first demyelinatingevent in approximately 20% of patients with MS.
Approximately 40% of these patients develop
optic neuritis. Characterized by loss of vision in the affected eye
and pain on movement of the eye.
Much less commonly, patients get phosphenes
(transient flashes of light or black squares) lasting
from hours to months. Phosphenes may occur before or duringan ON event or even several months following recovery.
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Partial acute transverse myelitis is usually amanifestation of multiple sclerosis. Acute
partial loss of motor, sensory, autonomic,
reflex, and sphincter function below the levelof the lesion indicates acute transverse
myelitis.
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Spasticity
Is characterized by increased muscle tone and
resistance to movement; it occurs most
frequently in muscles that function to
maintain upright posture. The muscle stiffness
greatly increases the energy expended to
perform activities of daily living (ADLs), whichin turn contributes to fatigue.
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Cognitive dysfunction
May occur early in the course of disease. Areas of
cognition affected may include any of the following:
Comprehension and use of speech
Attention
Memory Visual perception
Planning
Problem solving
Executive function (ability to correctly followsequential steps)
Abstract reasoning
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Pain in MS can be classified as primary or secondary.
Primary pain is related to the demyelinating processitself. This neuropathic pain is often characterized ashaving a burning, gnawing, or shooting quality.
Secondary pain in MS is primarily musculoskeletal innature and possibly results from poor posture, poorbalance, or abnormal use of muscles or joints as aresult of spasticity.
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Constipation
Constipation is the most frequent bowelcomplaint in patients with multiple sclerosis
and is characterized as the infrequent ordifficult passage of stools.
N/B Multiple sclerosis patients withadvancing disability and impaired bladderfunction may experience recurrent urinarytract infections.
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Heat intolerance
Persons with MS often experience an increase
in symptoms of fatigue or weakness when
exposed to high temperatures due to weather,exercise, hot showers or baths, or fever.
May result in blurring of vision (Uhthoff sign),
usually in an eye previously affected by opticneuritis. They typically reverse rapidly when exposure to hightemperature ends.
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HEREDITARY SPASTIC PARAPLEGIA
hereditary spastic paraplegia (HSP) is a
group of clinically and genetically diverse
disorders that cause progressive and
generally severe lower extremity weaknessand spasticity.
After normal gestation, delivery, and early
childhood development, subjects develop legstiffness and gait disturbance (eg, stumbling,
tripping) because of difficulty in dorsiflexing
the foot and as a result of weakness in hip
flexion.
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The classic symptom of HSP is progressive difficulty in
walking. Some patients eventually may require the useof a wheelchair, while others may never need any typeof assistive device. Patients usually have difficulty lifting their toes;as a result, they drag their toes when walking and catch them on stairs oron uneven sidewalks or curbs.
In later stages, patients complain of reduced sensationin the distal regions of the legs.
Some people also experience urinary problems egincontinence or a sense of urgency even when thebladder is not full
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Decreased sense of balance
A common symptom that the patient firstnotices.
Most of these patients have an impaired
sense of foot position. If the brain does notreceive accurate signals relating to the body's
position, it may not be able to respond
properly to those signals, and loss of balanceoccurs.
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In complicated HSP, a rare disorder, additionalsymptoms may include the following:
Peripheral neuropathy Epilepsy
Ataxia
Optic neuropathy
Retinopathy
Dementia
Ichthyosis Mental retardation
Deafness
Problems with speech, swallowing, or breathing
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ADEM
Clinically, acute disseminated encephalomyelitis (ADEM) isusually readily distinguishable from multiple sclerosis(MS) by the presence of certain clinical features, includingthe following:
History of preceding infectious illness or immunization
Association with constitutional symptoms and signs suchas fever
Prominence of cortical signs such as mental statuschanges and seizures
Comparative rarity of posterior column abnormalities,which are common in MS
Age younger than 11-12 years in ADEM and age olderthan 11-12 years in MS
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The mean age at presentation is about 7 years.
Typical cases of ADEM arise 1-20 days after a childhood
infectious illness, which is febrile in more than 94% ofcases. There is usually a clearly defined phase of afebrile improvement
lasting 1-20 days or more before onset of neurologic findings.
Documentation of at least 1 fever-free day is especially
suggestive of ADEM. Occasionally, ADEM may occur in the wake of several
weeks of fever of unknown origin.
Some patients have back pain prior to the development
of ADEM-related inflammatory myelitis. Various vaccines have been suggested as the exogenous
provocation of cases of ADEM and may account for 3-6%of ADEM cases.
evidence exists for the role of the Pasteur rabies vaccine
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The first signs of ADEM usually include abruptonset of irritability and lethargy (>94% of
cases).The onset of neurologic abnormalities isabrupt in more than 95% of ADEM cases.Occasionally, the development of diffuse marked neurologic abnormalitiesrequires only a few hours
Changes in mental status (88% of cases) arecommonly observed in ADEM.
Convulsive seizures occur around the onset ofADEM in as many as 25% of cases.
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ADEM-associated optic neuritis is usually
bilateral, although the onset in a second eye may
follow onset in the first by days to months. Opticneuritis in MS is frequently unilateral.
A wide variety of cranial nerve abnormalitiesmay occur in addition to optic nerve disease.
Long tract signs (eg, clonus, increased musclestretch reflexes, upgoing toes) are present early
in as many as 80% of cases.
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Fairly symmetric leg weakness is seen in many cases ofADEM-related transverse myelitis with associatedabnormalities of bowel and bladder function.
Most ADEM presentations may be summarized into 7clinical syndromes as follows: Mild encephalopathy, sometimes associated with long tract
signs
Severe encephalopathy with bilateral paresis, often associated
with brainstem signs, particularly the lower cranial nerves Predominantly brainstem presentation with features suggesting
Fisher syndrome in some cases
Hemiparesis, ipsilateral long tract signs, with or without seizure
ADEM-associated ataxia is often associated with nystagmus,
extremity ataxia, and long tract signs EMRN: Encephalomyeloradiculoneuropathy is a syndrome that
combines upper and lower motor neuron signs. EMRN maymanifest recurrences.
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SPINAL CORD INFARCTION
Spinal cord infarction is usually marked by anacute onset, often heralded by sudden andsevere spinal (back) pain, which may radiatecaudad.
This is associated with bilateral weakness,paresthesias, and sensory loss. Loss ofsphincter control with hesitancy and inabilityto void or defecate becomes evident within a
few hours. The spinal cord stroke, either ischemic or
hemorrhagic, has an acute onset evolvingover minutes.
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Spinal Arteries
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Neurologic deficit may occur without pain, butmost (>80%) spinal infarcts are painful. The mimicof coronary ischemia is seen because of the
occurrence of chest pain, which may be severe.
Uncomplicated spinal cord infarction is most
commonly thoracic
and presents as acuteparaparesis or paraplegia, numbness of the legs,and inability to void.
The syndrome depends on the level of the cordlesion and may vary from mild or moderate andeven reversible leg weakness to quadriplegia.
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Fever is a warning ("red flag"); consider infectious origins ofa spinal cord syndrome, particularly acute bacterialmeningitis, and focal extramedullary spinal lesions
(eg, epidural and subdural abscess, granuloma)and viralmyelitis due to herpes simplex.
Many reports exist, whereby cases of spinal cord infarctionoccur due to complications of surgical procedures in whichhypotension and prolonged positioning may be prominentfactors.
Also, aortic surgeries, injections for foraminal nerve block
for epidural anesthesia, or even self-injection by the addictseeking an intravenous accesshave been reported inassociation with and may be a causative of spinal cordinfarction.
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TRANSVERSE MYELITIS
Signs and symptoms of transverse myelitis usually develop over afew hours and worsen over a few days. Depending on the cause,one or both sides of the body may be affected.
Typical signs and symptoms include:
Pain.Pain associated with transverse myelitis often beginssuddenly in your neck or back, depending on the part of your spinalcord that's affected. Sharp, shooting sensations may also radiatedown your legs or arms or around your abdomen.
Abnormal sensations.Some people with transverse myelitis reportsensations of numbness, tingling, coldness or burning. Some areespecially sensitive to the light touch of clothing or to extreme heator cold.
Weakness in your arms or legs.Some people with mild weaknessnotice that they're stumbling or dragging one foot or that their legsfeel heavy as they move. Others may develop paralysis.
Bladder and bowel problems.These problems may include anincreased urinary urge, urinary incontinence, difficulty urinating andconstipation.
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Thank you..
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