Approach to the Patient with Upper Extremity Pain, Paresthesias, and Entrapment Neuropathies



Approach to the Patient with Upper Extremity Pain, Paresthesias, and Entrapment Neuropathies


Mark A. Ross



Upper extremity (UE) pain and paresthesias are common clinical complaints that often accompany reversible peripheral nervous system (PNS) or musculoskeletal (MSK) disorders. Common PNS disorders causing these symptoms include cervical radiculopathy, brachial plexopathy, and peripheral nerve entrapment syndromes (mononeuropathies). Muscle weakness and atrophy may complicate these PNS disorders but typically do not occur with MSK disorders. The location of symptoms and signs of these PNS disorders usually reflects PNS anatomy and thus helps to suggest the diagnosis. Electrodiagnostic studies (EDS) are regularly used to clarify a specific diagnosis. The causes of UE complaints can be determined by integrating clinical history, physical findings, and diagnostic study results.


I. DIFFERENTIAL DIAGNOSIS AND ETIOLOGY

Differential diagnosis and etiology of UE pain (see Table 24.1).


II. EVALUATION


A. History.


1. Symptoms.

The patient’s description of symptoms should be obtained. Clarification of reported symptoms is helpful as patients may misuse terms, for example, saying weakness to describe numbness. The examiner should inquire about symptoms in the unaffected UE and legs, as well as performing a general review of systems to address the possibility of a generalized process or a systemic disorder.



  • Sensory symptoms.



    • Pain. Pain descriptions are never pathognomonic of specific disorders. Tingling or radiating pain suggests a peripheral nerve, plexus, or root disorder, whereas dull, aching, nonradiating pain is typical of MSK disorders. Exceptions to this rule occur frequently. Acute onset of excruciating pain in the shoulder or arm is common with idiopathic brachial plexopathy. Pain radiating from the neck to the arm or hand suggests radiculopathy. The pain location may suggest the root involved—for example, lateral arm (C5), lateral forearm or thumb (C6), middle finger (C7), or medial hand and forearm (C8). Pain localized to the shoulder may result from MSK disorders, such as bicipital tendinitis, rotator cuff injury, and adhesive capsulitis, or from PNS disorders, such as C5 radiculopathy, brachial plexopathy, or entrapment of the suprascapular or dorsal scapular nerves (DSNs). Pain radiating distant from the site of pathology may belie the location—for example, carpal tunnel syndrome (CTS) occasionally manifests as forearm or shoulder pain. Forearm pain may occur with C6 radiculopathy, plexopathy, or nerve entrapment in the forearm. Pain involving specific digits may help localization. Pain involving the thumb, index finger, or middle finger suggests a median mononeuropathy, a C6 or C7 radiculopathy, or middle brachial plexus disorder. Pain involving the ring and little fingers suggests an ulnar mononeuropathy, a lower plexus disorder, or C8-T1 radiculopathy. Digital pain may also result from local MSK disorders—for example, arthritis. Bizarre descriptions of pain are typical of psychological or functional disorders.



    • Paresthesias and sensory loss. Paresthesias are spontaneous sensations originating from nerve fibers, which patients describe as “tingling” or “pins and needles.” Sensory loss indicates absence of normal sensation, which patients may describe as “numbness” or “like Novocain.” Paresthesias and sensory loss may occur together or independently, and either suggests that PNS disease is more likely than an MSK disorder. The distribution of paresthesias or sensory loss helps localize a nerve disorder. However, patients may report a distribution of sensory symptoms that varies from the precise anatomic distribution of an affected nerve or nerve root. Patients with CTS may complain of sensory symptoms in any of the first three hand digits and often report the entire hand is numb. Thus, failure of sensory symptoms to localize precisely to a specific nerve or nerve-root distribution should not exclude these disorders. The differential diagnosis of paresthesias and sensory loss should include CNS disease, especially when pain is absent. Intermittent paresthesias also occur in normal individuals, usually related to a specific activity or limb position resulting in nerve compression, stretch, or irritation. Thus, paresthesias in isolation do not always indicate a pathologic state


  • Motor symptoms. Patients complaining of weakness should be asked to describe specific activities that cause difficulty. Impaired fine motor skills—for example, buttoning buttons—indicate distal muscle weakness and suggest involvement of C8 or T1 roots, lower plexus, or nerves supplying hand muscles (median or ulnar nerves). Difficulty with arm and shoulder movements indicates proximal muscle weakness, suggesting involvement of the C5 or C6 roots, upper plexus, or nerves supplying proximal muscles (e.g., long thoracic, suprascapular, or axillary nerves). Patients with pain or sensory loss may misconstrue impaired motor performance as weakness. This possibility may be clarified during the exam or by asking the patient to state which factor chiefly limits physical performance. CNS disorders can also produce weakness of either the proximal or distal musculature.








TABLE 24.1 Differential Diagnosis and Etiology of UE Pain


























































































Disorder


Common Etiologies


PNS disorders


Radiculopathy


Root compression (disk and bone), trauma


Brachial plexopathy


Idiopathic, trauma, tumor, radiation, compressive (TOS)


Mononeuropathy



Suprascapular n.


Trauma, IBP



Dorsal scapular n.


Trauma, IBP



Long thoracic n.


Trauma, IBP



Musculocutaneous n.


Trauma, IBP



Median n.




Anterior interosseous n.


Compression, trauma




Pronator teres syndrome


Compression, trauma




CTS


Compression


Ulnar n.



Cubital tunnel syndrome


Compression, trauma



Guyon’s canal


Compression, trauma


Radial n.



Spiral groove


Compression, trauma



Posterior interosseous


Compression, trauma



Superficial radial


Compression, trauma


MSK disorders


Rotator cuff injury


Overuse, trauma


Biceps tendinitis


Overuse, trauma


Adhesive capsulitis


Immobility, shoulder weakness


Lateral epicondylitis


Overuse, trauma


Abbreviations: IBP, idiopathic brachial plexopathy; n. nerve.




2. Onset and precipitating factors.

The history should address specific activities the patient participated with during or just preceding the onset of symptoms and whether or not physical activity exacerbates the symptoms.



  • Physical activities. Some physical activities may predispose to specific PNS disorders. Heavy lifting may precipitate cervical disk herniation and resultant radiculopathy. Head turning often exacerbates pain or paresthesias associated with radiculopathy. Arm abduction or shoulder rotation exacerbates the pain of MSK shoulder disorders and also the pain associated with brachial plexopathy. Repetitive flexion and extension movements of the elbow or sustained elbow flexion may predispose to ulnar mononeuropathy at the elbow (cubital tunnel syndrome). Repetitive flexion and extension movements at the wrist or fingers may predispose to median mononeuropathy within the carpal tunnel (CTS). Repetitive pronation and supination may lead to hypertrophy of the pronator teres muscle and median nerve entrapment in the forearm (pronator teres syndrome). The radial nerve may be compressed in the axillary region by the improper use of a crutch, or in the arm when pressure is applied by a tourniquet, a hard surface, or the body’s weight. Radial nerve compression in the arm is especially likely to occur when consciousness is reduced by anesthesia, sedatives, or alcohol intoxication. Handcuffs or other tight-fitting objects at the wrist—for example, watchbands or bracelets—may injure the median, ulnar, or superficial radial sensory nerves. The history should include review of occupation, hobbies, and recent changes in physical activity. Sporting activities, playing musical instruments, gardening, and knitting are examples of physical activities that could predispose to compressive nerve injuries.


  • Trauma often causes UE pain and sensorimotor complaints. Even remote trauma may contribute to UE pain or sensorimotor symptoms. Examples include entrapment of a nerve by the callus of a healing fracture and development of a central cavity in the spinal cord (syringomyelia).



    • Motor vehicle accident (MVA). The severe trauma of a MVA may cause multiple neurologic complications including vertebral fracture with direct spinal cord injury, nerve-root avulsion, radiculopathy, brachial plexus injury, peripheral nerve injury, or late development of syringomyelia. Arm traction or stretching the arm and neck in opposite directions may cause cervical root avulsions or a stretch injury to the brachial plexus. An MVA may cause more than one PNS disorder—for example, cervical nerve-root avulsions and concomitant peripheral nerve injury. After an MVA, attention to multiple life-threatening injuries, or casting for multiple limb fractures, may preclude detection of PNS disorders until late in the course of recovery.


    • Fractures and dislocations may cause specific nerve injuries. Shoulder dislocation or fracture of the humerus may injure the axillary nerve. Fracture of the clavicle may injure components of the brachial plexus. Fracture of the humerus predisposes to radial nerve injury in the spiral groove, whereas fracture or dislocation of the radius may injure the posterior interosseous nerve (PIN) branch of the radial nerve. Fracture of the elbow predisposes to ulnar mononeuropathy, which may not manifest until years after the trauma, hence the name “tardy ulnar palsy.” A wrist fracture may cause either median or ulnar mononeuropathy.


    • Laceration. When UE pain or sensorimotor symptoms begin after a skin laceration or puncture wound, direct injury to a nerve needs to be considered. Exploration is needed to determine if the nerve requires repair.


  • Physiologic compression sites. The median and ulnar nerves are vulnerable to injury at specific sites where normal ligamentous and bony structures predispose to physical compression. The common compression sites are the wrist for the median nerve (carpal tunnel) and the elbow for the ulnar nerve (cubital tunnel). At these locations, the nerves are particularly susceptible to compression injury, hence the term “physiologic compression sites.” A patient with UE sensorimotor symptoms, without any clear predisposing factors, is likely to have an abnormality of one of these nerves.


  • Systemic illnesses. Systemic illness may predispose to the development of PNS disorders that manifest as UE sensorimotor symptoms. A complete listing of systemic
    illnesses with PNS complications exceeds the scope of this chapter, but several common examples are given.



    • Endocrine disorders. Patients with diabetic polyneuropathy are more vulnerable to development of mononeuropathies at physiologic compression sites. Patients with hypothyroidism are prone to developing CTS.


    • Rheumatologic disorders. Several rheumatologic disorders predispose to UE nerve or nerve-root injury. Rheumatoid arthritis causes joint and degenerative bone disease that may lead to cervical radiculopathy, CTS, and PIN injury. Systemic vasculitis may involve individual peripheral nerves in either the upper or lower extremities. Abrupt onset of a mononeuropathy is occasionally the presenting manifestation of systemic vasculitis. Primary and hereditary amyloidosis are associated with CTS.


    • Renal failure and dialysis. Patients receiving chronic hemodialysis are particularly likely to develop CTS, owing to the deposition of amyloid material (ß-2 microglobulin) within the carpal tunnel. Placement of arteriovenous fistulas for hemodialysis may cause median or ulnar neuropathies and, less often, a severe distal ischemic injury to all UE nerves, called ischemic monomelic neuropathy. Diabetic patients seem particularly prone to this severe nerve injury.


    • Malignancy. A patient with a history of cancer—particularly of the breast or lung—who develops UE sensorimotor complaints needs to be evaluated for metastases to the brachial plexus. Patients with radiation therapy to the brachial plexus region can develop radiation-induced brachial plexopathy, which may begin many years after radiation therapy.


3. Other history.

The medical history should also include inquiry about symptoms of depression and a review of the social situation for factors that might influence the patient’s symptoms. Specific questions should be asked regarding employment, accidents, work injuries, and possible litigation. Evidence of CNS disease should be sought, which might include seizures, disturbed consciousness, personality change, or problems with cognition, language, or vision.


B. Physical examination.


1. Motor examination.



  • Muscle inspection. Muscles are inspected for atrophy and spontaneous muscle contractions. Muscle atrophy is present when reduction of the normal muscle bulk is revealed by visual inspection or direct measurement of limb circumference. Atrophy of specific muscles helps localize the disorder. Atrophy of the thenar eminence alone suggests a disorder of the median nerve or the deep terminal branch of the ulnar nerve. Atrophy of the thenar and hypothenar areas and the interossei muscles should raise considerations of combined median and ulnar mononeuropathies, lower trunk brachial plexopathy, C8-T1 radiculopathy, or C8-T1 spinal cord disease. Winging or elevation of one scapula suggests a long thoracic nerve mononeuropathy. Muscle inspection also involves a careful search for fasciculations, which are fine muscle twitches visible through the skin. Fasciculations may occur infrequently as an isolated finding in asymptomatic individuals. However, when present in conjunction with muscle weakness and atrophy, fasciculations are a sign of a lower-motor neuron process. The exam should include inspection for fasciculations in all four limbs, as well as in the back and abdomen. Fasciculations occur most commonly with anterior horn cell diseases—for example, amyotrophic lateral sclerosis—but can also occur with diseases affecting the motor root, plexus, or peripheral nerve.


  • Muscle strength ratings. Muscle strength is assessed with manual muscle testing using the Medical Research Council strength rating scale (Table 22.1). It should be tested in proximal and distal muscles in all four limbs. This allows quantification of weakness and may reveal weakness the patient was not aware of. Muscles that should be tested bilaterally in the UE include muscles for arm abduction (deltoid and supraspinatus), arm external rotation (infraspinatus), elbow flexion (biceps), elbow extension (triceps), wrist flexion (flexor carpi radialis and flexor carpi ulnaris), wrist extension (extensor carpi radialis), finger flexion (flexor digitorum [FD] superficialis
    and FD profundis), finger extension (extensor digitorum communis), finger spreading (interossei), thumb abduction (abductor pollicis brevis), and grip strength.

    Patients with MSK disorders and patients with depression, psychological disturbances, or malingering may exhibit a type of weakness known as “breakaway” weakness, in which incomplete effort gives the appearance of weakness. Features suggesting breakaway weakness include pain complaints during testing, reasonable initial strength that decreases, variability in motor performance on serial exams, improved strength with encouragement, and absence of other objective signs of motor impairment. Patients with breakaway weakness due to a psychological disturbance or malingering often make facial expressions or body contortions to convey that great effort is being made.

    Only gold members can continue reading. Log In or Register to continue

    Stay updated, free articles. Join our Telegram channel

Aug 18, 2016 | Posted by in NEUROLOGY | Comments Off on Approach to the Patient with Upper Extremity Pain, Paresthesias, and Entrapment Neuropathies

Full access? Get Clinical Tree

Get Clinical Tree app for offline access