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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Distinguishing features between acute inflammatory demyelinating polyneuropathy (Guillain-Barré syndrome) and transverse myelitis

Distinguishing features between acute inflammatory demyelinating polyneuropathy (Guillain-Barré syndrome) and transverse myelitis
Characteristics Acute myelitis Guillain-Barré syndrome Distinguishing features
Motor findings Paraparesis or quadriparesis Ascending weakness LE>UE in the early stages

Myelopathy: if UE involvement, often as severe as LE; often no UE involvement.

GBS: there usually is UE involvement and it is less severe than LE involvement early in the disease.
Sensory findings Typically with a spinal cord sensory level demarcating intact (above) from diminished (below) pin and light touch sensation Ascending sensory loss LE>UE in the early stages

Myelopathy: sensory level usually identified; often no arm involvement.

GBS: no sensory level; usually UE less affected than LE early in the disease.
Autonomic findings Early loss of bowel and bladder control Autonomic dysfunction of the cardiovascular system

Myelopathy: urinary urgency or retention early and prominent; cardiovascular instability only in severe cases higher than T6 spinal level.

GBS: urinary urgency or retention less common; cardiovascular instability is more common.
Cranial nerve findings None Extra-ocular muscle palsies or facial weakness GBS: cranial neuropathies are more common than in acute myelopathy.
Electrophysiologic findings

EMG/NCS findings may be normal or may implicate the spinal cord

Prolonged central conduction on SEP latencies or missing SEP in conjunction with normal sensory nerve action potentials
EMG/NCS findings confined to the peripheral nervous system: motor and/or sensory nerve conduction velocity reduced, distal latencies prolonged; conduction block; reduced H reflex usually present

The lack of peripheral nerve abnormalities in a patient with progressive weakness and sensory loss should suggest evaluation of the spinal cord for pathology.

Conversely, patients with suspected acute myelopathy but equivocal clinical, laboratory, or radiologic findings may warrant peripheral nerve examination.
MRI findings Usually a focal area of increased T2 signal in the spinal cord, with or without gadolinium enhancement May be normal, or may reveal thickening and enhancement of the intrathecal spinal nerve roots and cauda equina. Abnormalities of the posterior columns are described in exceptional cases of Miller Fisher syndrome. MRI abnormalities may be helpful in diagnosing a patient who is suspected of having GBS from acute myelopathy.
CSF Usually, CSF pleocytosis and/or increased IgG index Usually, elevated protein in the absence of CSF pleocytosis CSF pleocytosis and elevated IgG index may be helpful in diagnosing a patient who is suspected of having GBS from acute myelopathy.
LE: lower extremity; UE: upper extremity; GBS: Guillain-Barré syndrome; EMG: electromyography; NCS: nerve conduction study; SEP: somatosensory evoked potentials; MRI: magnetic resonance imaging; CSF: cerebrospinal fluid; IgG: immunoglobulin G.
Graphic 88912 Version 4.0

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