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Peripheral nerve disorders

Peripheral nerve disorders

Peripheral nerve disorders

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Nerve Injury & Repair - Anatomy Under Attack

  • Nerve Sheaths

    • Epineurium: Dense connective tissue covering the entire peripheral nerve.
    • Perineurium: Surrounds nerve fascicles; forms the blood-nerve barrier.
    • Endoneurium: Surrounds individual axons and their Schwann cells.
  • Seddon Classification of Nerve Injury

TypeMyelin DamageAxon DamageSheath DamageRecovery
NeuropraxiaYesNoNoComplete
AxonotmesisYesYesNo (Endo intact)Good
NeurotmesisYesYesYesPoor/Incomplete
  • Wallerian Degeneration & Regeneration

⭐ Axonal regeneration in the PNS occurs at a rate of approximately 1 mm/day or 1 inch/month.

Guillain-Barré Syndrome - Ground-Up Invasion

  • Acute, immune-mediated demyelinating polyneuropathy, often post-infection (Campylobacter jejuni, viruses).
    • Pathogenesis involves molecular mimicry, targeting peripheral nerve myelin or axons.

Guillain-Barré Syndrome (GBS) symptoms and treatment

  • Clinical: Rapidly progressive, symmetric ascending weakness (📌 "ground-to-brain").
    • Starts in legs, ascends to arms, trunk, and face.
    • ↓ or absent deep tendon reflexes.
    • Autonomic dysfunction (tachycardia, BP changes) and respiratory failure are life-threatening complications.
  • Diagnosis & Management:
    • Nerve conduction studies show slowed velocity.
    • Treatment: IV immunoglobulin (IVIG) or plasmapheresis.

⭐ Key finding is albuminocytologic dissociation in CSF: markedly ↑ protein with a normal cell count, typically seen after the first week.

Chronic Neuropathies - Slow Burn & Wreckage

  • Diabetic Neuropathy: Most common cause of peripheral neuropathy.

    • Pathogenesis: Metabolic & vascular damage from chronic hyperglycemia. ↑Advanced glycation end products (AGEs) & sorbitol, ischemic injury to vasa nervorum.
    • Clinical: Distal, symmetric sensory or sensorimotor "stocking-and-glove" pattern. Autonomic neuropathy (gastroparesis, orthostatic hypotension) is common.
    • Morphology: Axonal degeneration. Hyalinization of endoneurial arterioles.
  • Charcot-Marie-Tooth (CMT) Disease: Most common hereditary peripheral neuropathy.

    • Pathogenesis: Genetic defects in myelin- or axon-related proteins (e.g., PMP22 duplication in CMT1A).
    • Clinical: Distal muscle atrophy (e.g., peroneal), sensory loss, pes cavus ("stork leg" deformity).
    • Morphology: Repetitive demyelination & remyelination forms concentric layers of Schwann cells.

Exam Favorite: The characteristic finding in demyelinating forms of CMT is "onion bulb" formation, visible on nerve biopsy, resulting from cycles of Schwann cell proliferation.

Pes cavus and distal muscle atrophy in Charcot-Marie-Tooth

High‑Yield Points - ⚡ Biggest Takeaways

  • Guillain-Barré syndrome is an acute, ascending paralysis, often post-Campylobacter infection, with albuminocytologic dissociation in CSF.
  • Diabetic neuropathy, the most common type, manifests as a distal, symmetric "stocking-glove" sensory loss.
  • Charcot-Marie-Tooth is a hereditary motor-sensory neuropathy causing pes cavus and distal muscle atrophy.
  • Wallerian degeneration refers to axonal breakdown distal to injury, with debris cleared by macrophages.
  • Segmental demyelination from Schwann cell damage slows nerve conduction velocity, a key feature in GBS.

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