Intramedullary Lesion, Diffuse/Ill-Defined Enhancement
Jeffrey S. Ross, MD
DIFFERENTIAL DIAGNOSIS
Common
Multiple Sclerosis
Transverse Myelitis (ATM)
ADEM
Viral Myelitis
Neuromyelitis Optica (NMO)
Less Common
Type I Spinal Dural A-V Fistula
Dural A-V Fistula (Brain)
Arterial Infarction
Spinal Cord Metastases
Astrocytoma
Rare but Important
Radiation Myelopathy
Abscess/Myelitis
Parasitic or Bacterial Infections
ESSENTIAL INFORMATION
Helpful Clues for Common Diagnoses
Multiple Sclerosis
Patchy or confluent enhancement
Cervical > thoracic
Small focal areas of T2 signal abnormality
Dorsal cord at C1-2 common location
Transverse Myelitis (ATM)
Can be secondary to known cause (e.g., MS, ADEM, cord ischemia)
Can be idiopathic (unknown cause) 15%
Thoracic > cervical
Imaging normal in up to 50%
ADEM
Immune-mediated, inflammatory white matter disorder
Para/post-infectious
Post-immunization
Typically monophasic illness
Any age (more common in child, young adult)
Brain affected more than spinal cord
Can be multifocal, patchy, or confluent
Check brain for multifocal white matter lesions with relatively little mass effect
Viral Myelitis
Acute/subacute viral infection (e.g., HIV, enteroviruses, HHSV6)
Usually multisegmental
Variable enhancement from subtle to profound
Neuromyelitis Optica (NMO)
Autoimmune, inflammatory disorder involving myelin of optic nerves and spinal cord
Longitudinally extensive (> 3 vertebral segments) T2 hyperintensity within cord
Presence of brain WM lesions does not exclude NMO
May reflect autoimmune targeting of Aquaporin-4 transmembrane channel proteins
Respiratory failure due to extensive cervical involvement in up to 1/3 cases (very uncommon in MS)
Radicular pain in 35% (uncommon in MS)
Lhermitte symptom common in MS and NMO
Helpful Clues for Less Common Diagnoses
Type I Spinal Dural A-V Fistula
Causes venous hypertension
Intradural flow voids on cord surface from arterialized veins
Swollen, edematous cord
Multisegmental T2 signal abnormality
Variable enhancement
Arterial Infarction
Sudden onset weakness, loss of sensation
Rapidly progressive
Causes
Anterior spinal or radicular artery occlusion
Hypotension
Thoracic (conus) > cervical
Nonspecific T2 hyperintensity ± ill-defined cord enhancement
Spinal Cord Metastases
Focal, enhancing cord lesion(s) with extensive edema
Lung, breast most common primary
Rapidly progressive flaccid paraparesis
Full craniospinal imaging when focal cord lesion found
Edema out of proportion to focal small cord lesion suggests metastasis, even if solitary
Astrocytoma
Helpful Clues for Rare Diagnoses
Radiation Myelopathy
Spindle-shaped cord swelling with irregular, focal rind of enhancement
Typically with doses over 50 Grey (Gy)
Demyelination in lateral, dorsal tracts
Concurrent chemotherapy may be a predisposing factor, especially if intrathecal
Parasitic or Bacterial Infections
Typical is well-defined, ring-enhancing mass within cord, with appropriate clinical history of inflammation/infection
More uncommon ill-defined or patchy enhancement
Schistosomiasis ill-defined punctate enhancement of conus
Other Essential Information
Long (multisegmental) cord enlargement with edema, patchy enhancement favors infection/inflammation over neoplasm
Do sagittal FLAIR or T2WI of brain in patients with unexplained myelopathy, cord lesions!
MS, ADEM usually have coexisting brain lesions
Alternative Differential Approaches
Acute transverse myelopathy
Includes both inflammatory and noninflammatory etiologies
Excludes compressive lesions
Differential considerations include
⇒ MS
⇒ Systemic disease
Sjögren, SLE
⇒ Vascular
⇒ Parainfectious (ADEM)
⇒ Radiation myelopathy
⇒ Idiopathic
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