Diagnosis of brachial and lumbosacral plexus lesions.

Handb Clin Neurol

Department of Neurology and Clinical Neurophysiology, Radboud University Nijmegen Medical Centre, The Netherlands. Electronic address:

Published: April 2014

AI Article Synopsis

  • Brachial and lumbosacral plexopathies are complex disorders due to their intricate anatomy and rarity, making them challenging for doctors to diagnose.
  • Common causes include neuralgic amyotrophy for brachial plexopathy and diabetic amyotrophy for lumbosacral plexopathy, while traumatic and malignant cases are less frequent but severe.
  • The chapter emphasizes the importance of clinical examination, diagnostic techniques, prognosis, and treatment options for these conditions.

Article Abstract

To most doctors, brachial and lumbosacral plexopathies are known as difficult disorders, because of their complicated anatomy and relatively rare occurrence. Both the brachial, lumbar, and sacral plexuses are extensive PNS structures stretching from the neck to axillary region and running in the paraspinal lumbar and pelvic region, containing 100000-200000 axons with 12-15 major terminal branches supplying almost 50 muscles in each limb. The most difficult part in diagnosing a plexopathy is probably that it requires an adequate amount of clinical suspicion combined with a thorough anatomical knowledge of the PNS and a meticulous clinical examination. Once a set of symptoms is recognized as a plexopathy the patients' history and course of the disorder will often greatly limit the differential diagnosis. The most common cause of brachial plexopathy is probably neuralgic amyotrophy and the most common cause of lumbosacral plexopathy is diabetic amyotrophy. Traumatic and malignant lesions are fortunately rarer but just as devastating. This chapter provides an overview of both common and rarer brachial and lumbosacral plexus disorders, focusing on clinical examination, the use of additional investigative techniques, prognosis, and treatment.

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http://dx.doi.org/10.1016/B978-0-444-52902-2.00018-7DOI Listing

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