n_neuropathies
Table of Contents
Neuropathies
see neurology
Mononeuropathies:
definition:
- lesions of individual nerve bundles
aetiology:
- trauma, compression
- causes that may result in more than one nerve affected (ie. mononeuritis multiplex):
- acute (usually vascular):
- diabetes mellitus
- polyarteritis nodosa, SLE, Rh.A
- chronic:
- multiple compressive neuropathies, esp. with joint deforming arthritis
- sarcoid
- amyloid
- acromegaly
- Lyme disease
- leprosy
- neoplasia (rare)
common nerves involved:
- median nerve
- ulnar nerve
- radial nerve
- sciatic nerve
- lateral popliteal nerve
- tibial nerve
Polyneuropathies:
introduction:
- derangements of peripheral nerves which usually begin distally & spread proximally giving rise to 'glove & stocking' anaesthesia (peripheral neuropathy)
- distal motor weakness may also occur, & reflexes reduced
- different patterns are discernible with different causes
- pain & tenderness in affected muscles is notable in neuropathies of diabetes & alcoholics
aetiology:
- common causes of peripheral neuropathy:
- Guillain-Barre syndrome
- metabolic:
- diabetes mellitus, renal failure, liver failure, alcohol, hypothyroidism, porphyria, hypoglycaemia xanthomatosis
- CT diseases:
- polyarteritis nodosa
- malignancy:
- incl. polycythaemia rubra vera
- infections:
- esp. leprosy, TB, syphilis
- vitamin deficiencies:
- B1
- B6
- B12 (subacute combined degeneration of the cord):
- symmetric post. column loss (vibration & position sense) ⇒ ataxic gait
- symmetric UMN signs in lower limbs with absent ankle jerks
- knee reflexes may be absent, or, more often, exaggerated
- peripheral sensory neuropathy (less common & mild)
- optic atrophy, dementia
- genetic:
- Refsum's syndrome
- Charcot-Marie-Tooth syndrome (HMSN Type I):
- pes cavus, distal muscle atrophy, absent reflexes, thickened nerves, optic atrophy
- toxins:
- lead, metronidazole, phenytoin, vincristine, nitrofurantoin, amiodarone
predominantly motor peripheral neuropathy:
- Guillain-Barre syndrome
- Charcot-Marie-Tooth syndrome
- acute intermittent porphyria
- lead poisoning
- diabetes
- NB. remember MND & NM junction disorders
predominantly sensory peripheral neuropathy
- unusual & results in sensory ataxia & pseudoathetosis
- carcinoma eg. lung, ovary, breast
- paraproteinaemia
- B6 intoxication
- Sjogren's syndrome
- diabetes
- syphilis
- B12 deficiency (occas)
painful peripheral neuropathy:
- diabetes
- alcohol
- B12 or B1 deficiency
- carcinoma
- porphyria
- arsenic or thallium poisoning
- hereditary
- NB. burning soles of feet may be painful periperal neuropathy, tarsal tunnel syndrome or an S1 lesion
extensor plantar response with absent ankle jerks:
- B12 deficiency
- conus medullaris lesion
- UMN lesion + cauda equina compression or peripheral neuropathy
- syphilis (tabo-paresis)
- Friedrich's ataxia
- diabetes (uncommon)
- adrenoleukodystrophy or metachromatic leukodystrophy
rapid onset neuropathies (within days)
- ischaemic
- pressure - direct pressure on a nerve; compartment syndrome; etc.
- iatrogenic - injection into nerves
- penetrating wounds or thermal injury
- polyarteritis nodosa
- rheumatoid arthritis
- diabetic cranial neuropathies
- diabetic amyotrophy
- Guillain-Barré syndrome
- Acute intermittent porphyria
- Critical illness polyneuropathy
- Diphtheric neuropathy
- thallium toxicity
subacute onset (weeks to months)
- Maintained exposure to toxic agents/medications
- Persisting nutritional deficiency
- Abnormal metabolic state
- Paraneoplastic syndrome
- chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)
insidious onset with chronic course
- Hereditary motor sensory neuropathies
- Dominantly inherited sensory neuropathy
- chronic inflammatory demyelinating polyradiculoneuropathy
relapsing/remitting course
- Guillain-Barré syndrome
- chronic inflammatory demyelinating polyradiculoneuropathy
- HIV/AIDS
- toxic
- porphyria
investigations:
- FBE, ESR, glucose, U&E, TFT, B12, protein electrophoresis, syphilis serology, ANA, CXR
- consider: porphyria screen; nerve conduction studies & electromyography
treatment:
- Rx cause
Multiple cranial nerve palsies:
- see also bulbar palsy
aetiology:
- think of malignancy first
- nasopharyngeal carcinoma
- chronic meningitis eg. carcinoma, TB, sarcoid
- Guillain-Barre syndrome (usually spares I, II, & VIII)
- brainstem lesions:
- usually due to vascular disease causing crossed sensory or motor paralysis(ie. cranial nerve lesions on one side & contralateral long tract signs)
- pts with brainstem gliomas may have similar signs & may live for many years
- Arnold Chiari malformation - protrusion of the cerebellar tonsils through the foramen magnum, with the more severe types (II to IV) which may cause lower cranial nerve palsies, cerebellar limb signs & upper motor neurone signs in legs
- trauma
- lesion of base of skull (eg. Paget's disease, metastasis)
- rarely, mononeuritis multiplex (eg. diabetes)
References
n_neuropathies.txt · Last modified: 2017/10/02 13:13 by 127.0.0.1