Antecedent Minor Trauma and Hyperacute Presentations in Childhood Transverse Myelitis

Jocelyn Lim1, Ehab Shaban Hamouda2, Marielle Valerie Fortier3

  • 1Neurology Service, Department of Paediatric Medicine, 37579KK Women's and Children's Hospital, Singapore.

Insights

Minor trauma or hyperacute onset in children with transverse myelitis does not always mean fibrocartilaginous embolism or spinal cord infarction. These children often have a distinct syndrome with good outcomes after immunotherapy.

Area of Science:

  • Pediatric Neurology
  • Neuroscience
  • Spinal Cord Disorders

Background:

  • Fibrocartilaginous embolism and spinal cord infarction can mimic transverse myelitis, particularly after minor trauma or with hyperacute onset.
  • Differentiating these conditions is crucial for appropriate diagnosis and management in pediatric patients.

Purpose of the Study:

  • To investigate the clinical and neuroimaging characteristics of transverse myelitis in children with antecedent minor trauma or hyperacute presentation.
  • To compare outcomes between children with and without these specific clinical features.

Main Methods:

  • A 10-year cohort study (2007-2016) of children (1 month to 16 years) diagnosed with transverse myelitis.
  • Application of diagnostic criteria for fibrocartilaginous embolism and spinal cord infarction.
  • Comparison of clinical, laboratory, neuroimaging, and outcome data based on the presence of antecedent minor trauma or hyperacute onset.

Main Results:

  • Of 32 children, 10 (31%) had antecedent minor trauma and 6 (19%) had hyperacute presentations.
  • Only one patient met spinal cord infarction criteria; none had fibrocartilaginous embolism.
  • Children with minor trauma preceding transverse myelitis showed distinct clinicoradiologic features, including single, short spinal cord lesions, and generally good outcomes (80%) after immunotherapy.

Conclusions:

  • Antecedent minor trauma or hyperacute onset in pediatric transverse myelitis does not invariably indicate fibrocartilaginous embolism or spinal cord infarction.
  • A distinct clinicoradiologic syndrome is observed in children with minor trauma preceding transverse myelitis.
  • This specific group demonstrates favorable outcomes with immunotherapy.
Abstract

Related Concept Videos

Poliomyelitis01:17

Poliomyelitis

Poliomyelitis is caused by poliovirus, a small, non-enveloped, positive-sense RNA virus of the Picornaviridae family and Enterovirus genus. Transmission occurs primarily via the fecal-oral route, often through ingestion of contaminated water or food. The virus initially replicates in the oropharynx and intestinal mucosa, particularly in lymphoid tissues such as the tonsils, Peyer’s patches, and regional lymph nodes. Primary viremia follows, allowing dissemination throughout the body.In most...
Bacterial Meningitis I: Introduction01:22

Bacterial Meningitis I: Introduction

Bacterial meningitis is a severe, life-threatening inflammation of the meninges, particularly the pia mater and arachnoid mater, affecting the subarachnoid space, ventricles, and cerebrospinal fluid (CSF). If untreated, it can lead to significant neurological complications or death.Causative AgentsCommon pathogens vary with age and immune status. In adults, major organisms include Streptococcus pneumoniae, Neisseria meningitidis, and Haemophilus influenzae. Streptococcus agalactiae (group B...
Encephalitis l: Introduction01:19

Encephalitis l: Introduction

Encephalitis is inflammation of the brain parenchyma, most often due to infections or autoimmune processes. It presents with neuropsychiatric features such as fever, altered mental status, behavioral changes, cognitive dysfunction, seizures, focal deficits, and sometimes autonomic instability. In some cases, the meninges are also involved, resulting in meningoencephalitis.Infectious CausesInfectious encephalitis is most commonly viral but can also result from bacterial, fungal, or parasitic...
Encephalitis ll: Pathophysiology01:26

Encephalitis ll: Pathophysiology

Encephalitis is inflammation of the brain parenchyma caused by direct viral invasion or immune-mediated mechanisms triggered by infections or tumors. Both processes lead to neuronal injury, disrupted neurotransmission, and diverse neurological symptoms, often with overlapping clinical and pathological features.Autoimmune EncephalitisIn autoimmune encephalitis, antibodies target neuronal antigens on cell surfaces, synapses, or within neurons. A key example is anti-NMDAR encephalitis, which can...
Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
Secondary Spinal Cord Injury llI: Pathophysiology01:25

Secondary Spinal Cord Injury llI: Pathophysiology

Early Ischemia and Ionic ImbalanceWithin minutes of spinal cord injury, a secondary cascade begins, progressing over hours to weeks. Vascular damage reduces blood flow, causing ischemia and mitochondrial dysfunction. ATP depletion leads to ion pump failure, membrane depolarization, sodium influx, potassium efflux, and water accumulation, resulting in cellular swelling. Increased intracellular calcium further disrupts mitochondria and accelerates cellular injury.Excitotoxicity and Neuronal...