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