Pronator teres syndrome

Changed by Mark Thurston, 3 Feb 2018

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Pronator teres syndrome (also called pronator syndrome) is one of three common median nerve entrapment syndromes; the other two being anterior interosseous nerve syndrome and the far more common carpal tunnel syndrome. It comprises a constellation of signsSigns and symptoms that result from compression of the median nerve in the upper forearm 1.

Epidemiology

PTS aPronator teres syndrome is rare entrapment syndrome but is most common in women past. Women over the age of 40 are more frequently affected.

Clinical presentation

PTS canPatients may present with 5 :  

  • volar pain of the proximal lower arm
  • paresthesia of the volar forearm and the radial three digits and radial aspect of the fourth digit
  • weakness, on the other hand, is variable, often with unspecified grip clumsiness
  • the proximal volar forearm is painful to palpation, and Tinel’s sign can be elicited on palpation of the pronator teres muscle

Symptoms provoked by examination maneuvers, such as during resisted forearm pronation (suggesting median nerve compression by pronator teres muscle), or resisted elbow flexion and forearm supination (indicating median nerve compression by biceps aponeurosis / lacertus fibrosus) can help pinpoint the site of compression.5

Clinical presentation can harbor some pitfalls. Sensory and pain symptoms of PTS and carpal tunnel syndrome can overlap: distinguish the two by looking for numbness of the forearm, which does not occur in CTS, and asking about nocturnal exacerbation, which would atypical in PTS. Provocation tests as detailed above can help further.

Pathology

The median nerve can be involved at several locations around the elbow 5:

Distribution

In complete PTSpronator teres syndrome, affected muscles are the pronator teres (PT), flexor carpi radialis (FCR), palmaris longus (PL), flexor digitorum superficialis (FDS), along with muscles innervated by the anterior interosseous nerve

Radiographic features

Ultrasound and MRI are the two imaging modalities which best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes [e.g. primary nerve or sheath tumors, ganglion cysts, osseous spurs, anatomical variants (e.g. Gantzer muscle), recognising pathological muscle signal patterns on MRI can inversely point to the affected nerve.

MRI

Look for the pattern of muscle signal changes on fluid-sensitive (STIR, PD, or T2W fat sat) sequences to uncover the affected nerve. 

In PTS, the pronator teres (PT), flexor carpi radialis (FCR), palmaris longus (PL), flexor digitorum superficialis (FDS) will reveal hyperintense signal changes secondary to denervation oedema, which can occur 24-48 hours after an inciting event; electromyography, the most sensitive neurophysiological study for inferring denervation syndromes, needs 7-14 days to show pattern changes.

Treatment

PTS canConservative treatment may be treated conservativelyeffective in 50–70% of cases with extremity rest and NSAR; corticosteroidsnon-steroidal anti-inflammatory drugs. Corticosteroids have also been used, as well. Surgical decompression is indicated in space-occupying lesions and failure of conservative treatment over 12 weeks, with success rates of up to 90% 6.

Differential diagnosis

Pronator-teres syndrome must be differentially diagnosed from:

See also

  • -<p><strong>Pronator teres syndrome </strong>(also called <strong>pronator syndrome</strong>) is one of three common <a href="/articles/median-nerve-entrapment-syndromes">median nerve entrapment syndromes</a>; the other two being <a href="/articles/anterior-interosseous-nerve-syndrome-1">anterior interosseous nerve syndrome</a> and the far more common <a href="/articles/carpal-tunnel-syndrome-1">carpal tunnel syndrome</a>. It comprises a constellation of signs and symptoms that result from compression of the median nerve in the upper forearm <sup>1</sup>.</p><h4>Epidemiology</h4><p>PTS a is rare entrapment syndrome but is most common in women past 40.</p><h4>Clinical presentation</h4><p>PTS can present with <sup>5</sup> :  </p><ul>
  • +<p><strong>Pronator teres syndrome </strong>(also called <strong>pronator syndrome</strong>) is one of three common <a href="/articles/median-nerve-entrapment-syndromes">median nerve entrapment syndromes</a>; the other two being <a href="/articles/anterior-interosseous-nerve-syndrome-1">anterior interosseous nerve syndrome</a> and the far more common <a href="/articles/carpal-tunnel-syndrome-1">carpal tunnel syndrome</a>. Signs and symptoms result from compression of the <a title="Median nerve" href="/articles/median-nerve-2">median nerve</a> in the upper forearm <sup>1</sup>.</p><h4>Epidemiology</h4><p>Pronator teres syndrome is rare. Women over the age of 40 are more frequently affected.</p><h4>Clinical presentation</h4><p>Patients may present with <sup>5</sup> :  </p><ul>
  • -<li>distal <a href="/articles/humerus">humerus</a>: avian spur and <a href="/articles/supracondylar-spur">ligament of Struthers</a>
  • -</li>
  • +<li>distal humerus: <a title="Avian spur" href="/articles/supracondylar-spur">avian spur</a> and ligament of Struthers</li>
  • -</ul><h5><strong>Distribution</strong></h5><p>In complete PTS, affected muscles are the pronator teres (PT), <a href="/articles/flexor-carpi-radialis">flexor carpi radialis</a> (FCR), <a href="/articles/palmaris-longus">palmaris longus</a> (PL), <a href="/articles/flexor-digitorum-superficialis">flexor digitorum superficialis</a> (FDS), along with muscles innervated by the anterior interosseous nerve. </p><h4>Radiographic features</h4><p>Ultrasound and MRI are the two imaging modalities which best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes [e.g. primary nerve or sheath tumors, ganglion cysts, osseous spurs, anatomical variants (e.g. Gantzer muscle), recognising pathological muscle signal patterns on MRI can inversely point to the affected nerve.</p><h5>MRI</h5><p>Look for the pattern of muscle signal changes on fluid-sensitive (STIR, PD or T2W fat sat) sequences to uncover the affected nerve. </p><p>In PTS, the pronator teres (PT), flexor carpi radialis (FCR), palmaris longus (PL), flexor digitorum superficialis (FDS) will reveal hyperintense signal changes secondary to denervation oedema, which can occur 24-48 hours after an inciting event; electromyography, the most sensitive neurophysiological study for inferring denervation syndromes, needs 7-14 days to show pattern changes.</p><h4>Treatment</h4><p>PTS can be treated conservatively in 50–70% of cases with extremity rest and NSAR; corticosteroids have been used, as well. Surgical decompression is indicated in space-occupying lesions and failure of conservative treatment over 12 weeks, with success rates of up to 90% <sup>6</sup>.</p><h4>Differential diagnosis</h4><p>Pronator-teres syndrome must be differentially diagnosed from:</p><ul>
  • +</ul><h5><strong>Distribution</strong></h5><p>In complete pronator teres syndrome, affected muscles are the pronator teres (PT), <a href="/articles/flexor-carpi-radialis">flexor carpi radialis</a> (FCR), <a href="/articles/palmaris-longus">palmaris longus</a> (PL), <a href="/articles/flexor-digitorum-superficialis">flexor digitorum superficialis</a> (FDS), along with muscles innervated by the <a title="Anterior interosseous nerve" href="/articles/anterior-interosseous-nerve">anterior interosseous nerve</a>. </p><h4>Radiographic features</h4><p>Ultrasound and MRI are the two imaging modalities which best lend themselves to investigating entrapment syndromes. Next to directly visualising direct causes [e.g. primary nerve or sheath tumors, ganglion cysts, osseous spurs, anatomical variants (e.g. Gantzer muscle), recognising pathological muscle signal patterns on MRI can inversely point to the affected nerve.</p><h5>MRI</h5><p>Look for the pattern of muscle signal changes on fluid-sensitive (STIR, PD, or T2W fat sat) sequences to uncover the affected nerve. </p><p>In PTS, the pronator teres (PT), flexor carpi radialis (FCR), palmaris longus (PL), flexor digitorum superficialis (FDS) will reveal hyperintense signal changes secondary to denervation oedema, which can occur 24-48 hours after an inciting event; electromyography, the most sensitive neurophysiological study for inferring denervation syndromes, needs 7-14 days to show pattern changes.</p><h4>Treatment</h4><p>Conservative treatment may be effective in 50–70% of cases with extremity rest and non-steroidal anti-inflammatory drugs. Corticosteroids have also been used. Surgical decompression is indicated in space-occupying lesions and failure of conservative treatment over 12 weeks, with success rates of up to 90% <sup>6</sup>.</p><h4>Differential diagnosis</h4><p>Pronator-teres syndrome must be differentially diagnosed from:</p><ul>

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