Carpal tunnel syndrome (CTS) is compression of the median nerve at the wrist. It is the commonest entrapment neuropathy, affecting roughly 3-6% of UK adults, with a female preponderance (3:1) and peak incidence between 40 and 60 years. Risk factors include pregnancy, obesity, diabetes, hypothyroidism, rheumatoid arthritis, and repetitive forceful wrist activity. Most cases are idiopathic and respond to conservative measures, but persistent or progressive disease threatens permanent motor and sensory loss in the median distribution.
The carpal tunnel is a fibro-osseous canal at the wrist bounded by the carpal bones dorsally and the flexor retinaculum (transverse carpal ligament) volarly. It transmits the median nerve and nine flexor tendons (four FDS, four FDP, and FPL). The space is unforgiving: any reduction in cross-sectional area or increase in content compresses the nerve.
Pathophysiology is mechanical compression and microvascular ischaemia of the median nerve. Sustained pressure raises intraneural pressure, reduces endoneurial blood flow, and triggers focal demyelination of the largest myelinated fibres first. With time, axonal loss follows, with motor fibres particularly vulnerable. Pressure rises with wrist flexion or extension, explaining the night-time and provocation-related symptoms. The recurrent motor branch supplies the thenar muscles and is the first motor casualty.
The recurrent motor branch of the median nerve exits radially from the main trunk just distal to the flexor retinaculum, supplying abductor pollicis brevis (APB), opponens pollicis, and the superficial head of flexor pollicis brevis. Thenar wasting and weak APB are late but important findings.
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