What are the clinical manifestations of Acute Transverse Myelitis (ATM)?

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Clinical Manifestations of Acute Transverse Myelitis

Acute Transverse Myelitis (ATM) typically presents with a combination of motor weakness, sensory symptoms, and bowel/bladder dysfunction that develops over hours to days, with progression to maximum severity within 4 hours to 21 days.

Core Clinical Manifestations

Motor Symptoms

  • Bilateral limb weakness (paraparesis or quadriparesis)
  • Rapidly progressive paralysis
  • Spasticity
  • Hyperreflexia
  • Positive Babinski signs

Sensory Symptoms

  • Sensory level deficit (clear demarcation of sensory loss below a specific spinal level)
  • Paresthesias
  • Numbness
  • Pain (often radicular or band-like around the trunk)
  • Loss of vibration and proprioception

Autonomic Dysfunction

  • Urinary retention or incontinence
  • Bowel dysfunction (constipation or incontinence)
  • Sexual dysfunction
  • Cardiovascular instability in high cervical lesions

Specific Presentations Based on Lesion Level

Cervical Lesions

  • Quadriparesis/quadriplegia
  • Respiratory insufficiency (may require ventilatory support if vital capacity falls below 15 ml/kg) 1
  • Diaphragmatic weakness
  • Four-limb sensory disturbances

Thoracic Lesions

  • Paraparesis/paraplegia
  • Truncal sensory level
  • Preserved upper limb function
  • Thoracic band-like pain

Temporal Profile

  • Acute onset: Symptoms develop over hours to days
  • Progression to nadir: 4 hours to 21 days 2
  • May be preceded by prodromal illness (fever, respiratory or gastrointestinal infection) in 30-60% of cases

Diagnostic Indicators

MRI Findings

  • Longitudinally extensive spinal cord lesion (≥3 vertebral segments) 3
  • T2 hyperintensity within the spinal cord
  • Spinal cord swelling
  • Gadolinium enhancement may be present

CSF Abnormalities

  • Neutrophilic pleocytosis 3
  • Elevated protein levels
  • Absence of oligoclonal bands (helps distinguish from multiple sclerosis)

Variants and Associated Conditions

ATM may present as part of:

  • Idiopathic ATM (most common)
  • Multiple sclerosis
  • Neuromyelitis optica spectrum disorders (check for AQP4-IgG)
  • MOG-antibody associated disease
  • Post-infectious/parainfectious myelitis
  • Systemic autoimmune diseases (SLE, Sjögren's syndrome) 4
  • Paraneoplastic syndromes

Severity Indicators and Prognostic Factors

Poor prognostic factors include:

  • Rapid progression to maximum deficit (<24 hours)
  • Complete paralysis
  • Sphincter dysfunction at onset
  • Extensive lesions on spinal MRI
  • Delayed treatment initiation 1

Complications

  • Respiratory failure (in high cervical lesions)
  • Pressure ulcers
  • Deep vein thrombosis
  • Urinary tract infections
  • Spasticity
  • Neuropathic pain
  • Permanent disability

Diagnostic Criteria

The diagnosis of ATM requires all of the following 5:

  1. Bilateral signs/symptoms attributable to spinal cord dysfunction
  2. Clearly defined sensory level
  3. Progression to maximum deficit between 4 hours and 21 days
  4. Evidence of inflammation within the spinal cord (CSF pleocytosis, elevated IgG index, or MRI enhancement)
  5. Exclusion of compressive, vascular, infectious, and other causes

Early recognition of these clinical manifestations is critical for prompt diagnosis and treatment initiation, which may significantly impact long-term outcomes and reduce permanent disability 6.

References

Guideline

Treatment of Paget's Disease with Chronic Demyelinating Neuropathy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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