Differentials

Myelopathy due to cervical spondylosis

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

The patient's symptoms and signs are all below the neck (although they may have dizziness and headache).

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MRI of the cervical spine shows compression of the spinal cord.

Fibromyalgia

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SIGNS / SYMPTOMS

Generalised weakness and non-specific fatigue are common.

Neurological examination is normal apart from possible functional overlay.

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MRI brain may show non-specific white matter changes, but not the characteristic MS findings.

Postural orthostatic tachycardia syndrome with or without cervicogenic migraine

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

History is significant for headaches and dizziness, particularly with change of head position or standing. Examination is normal.

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MRI of the cervical spine may show cervical spondylosis.

Tilt table testing may be abnormal.

Sleep disorders

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Patient describes non-restful sleep with variable features of snoring, restless legs, and apnoea. Memory changes and mood disturbances may be prominent. Neurological examination is normal.

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Abnormal sleep study.

Sjogren syndrome

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Symptoms of dry eyes and dry mouth as well as joint stiffness and pain. Neurological examination is usually normal.

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Elevated autoantibodies (anti-Ro/SSA and anti-La/SSB).

MRI brain and spinal cord are normal.

Vitamin B12 deficiency

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Numbness, fatigue, and possible memory loss. Posterior column loss of sensation (vibration and proprioception) in the presence of increased reflexes on examination.

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Low vitamin B12 level, high methylmalonic acid level.

MRI does not show characteristic lesions of MS.

Ischaemic stroke

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

History indicates sudden onset of symptoms. Signs and symptoms usually explainable on the basis of a single neurological lesion, rather than multiple lesions.

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CT head shows ischaemic changes.

Diffusion-weighted MRI will be abnormal in the acute setting.

Peripheral neuropathy

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Loss of sensation and reflexes in the feet and hands if large nerve fibre, severe pain if small nerve fibre.

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Abnormal electromyogram if large nerve fibre, abnormal skin biopsy for number of nerve fibres if small fibre.

Blood tests for specific cause (e.g., haemoglobin A1c [HbA1c] or thyroid-stimulating hormone) are abnormal.

Lymphoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Patient has gradual onset of severe disability.

INVESTIGATIONS

MRI shows persistent enhancing lesion over time, which may worsen despite treatment.

Neoplastic cells seen on cerebrospinal fluid cytology.

Inherited disorders such as mitochondrial diseases and leukodystrophies

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SIGNS / SYMPTOMS

Patient has gradual onset of memory or cognitive problems, sometimes in the setting of neuropathy.

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MRI appearance is quite distinct and includes prominent symmetrical white matter changes and normal spinal cord MRI.

Some blood tests are available for specific disorders.

Sarcoidosis

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Patient may have prior history of pulmonary sarcoid and shortness of breath.

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Highly elevated serum ACE level.

Abnormal chest x-ray and gallium scans.

MRI brain non-specific white matter changes; MRI brain or spinal cord may show meningeal enhancement.

Guillain-Barre syndrome

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Loss of reflexes with predominantly motor symptoms. Dangerous respiratory complications are more common.

INVESTIGATIONS

MRI is normal.

Cerebrospinal fluid shows characteristic cytoalbumin dissociation, and the classical MS findings of oligoclonal bands and elevated IgG and IgG synthesis are absent.

Amyotrophic lateral sclerosis (ALS)

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Mixed upper and lower motor neuron signs are present: increased reflexes (upper motor neuron) with atrophy and fasciculations (lower motor neuron).

Visual changes are absent.

ALS may involve dysphagia and pulmonary function abnormalities, but the dysphagia, unlike in MS, is usually accompanied by tongue fasciculations and dysphonia.

INVESTIGATIONS

Electromyogram is diagnostic of ALS. It is normal in MS unless there is a comorbidity such as diabetes or B12 deficiency.

Compressive lesions may resemble ALS and MRI of the spinal cord is recommended to exclude compressive syndromes; if MS is present, characteristic lesions are usually seen on MRI.

Muscle biopsies are useful to exclude primary muscle pathology.

Systemic lupus erythematosus

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Patient may have fevers, joint pain and swelling, muscle tenderness, (malar) rash.

INVESTIGATIONS

Elevated anti-nuclear antibodies (however, it is common to have mild elevation in MS), positive anti-DS DNA.

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