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A Toddler With New Seizures, Progressive White Matter Lesions, and Multifocal Microhemorrhages
Dana Tlais1, Stephanie Fetzko1, Nitya Gulati1
1Pediatric Hematology/Oncology.
Insights
A previously healthy child developed severe neurological symptoms including seizures and motor deficits following an enterovirus infection. Specialized testing revealed a rare condition, highlighting diagnostic challenges in atypical pediatric cases.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Neuroimaging
Background:
- A 16-month-old male presented with new-onset seizures and was found to have an enterovirus/rhinovirus infection.
- Initial workup revealed white matter abnormalities, microhemorrhages on MRI, liver enzyme elevation, and low platelets.
Observation:
- Symptoms initially improved with steroid therapy but recurred with motor deficits upon steroid tapering.
- Repeat MRI showed significant progression of white matter lesions and microhemorrhages.
- The patient developed fever, seizure recurrence, cerebral salt wasting, encephalopathy, cerebral edema, and diffuse brain injury.
Findings:
- A rare condition was suspected and confirmed through specialized testing.
- The case highlights diagnostic challenges posed by atypical presentations and modified disease progression.
Implications:
- This case underscores the importance of considering rare conditions in pediatric neurological emergencies.
- Understanding atypical presentations and the impact of interventions is crucial for accurate diagnosis and management.
- Advances in neuroimaging and specialized diagnostics are vital for identifying uncommon neurological disorders in children.
Abstract:
A 16-month-old, previously healthy male is hospitalized for new onset seizures. Initial investigation is significant for enterovirus/rhinovirus respiratory infection, abnormal T2 signal predominantly in the white matter and scattered microhemorrhages on brain MRI, transaminitis, and thrombocytopenia. His symptoms initially improve on steroid therapy and he is discharged from the hospital. During the ensuing month with the tapering of the steroids, he develops new motor deficits for which he is rehospitalized. His laboratory investigation on readmission is unremarkable. However, there is significant progression of white matter lesions and microhemorrhages on repeat MRI. While in the hospital, he becomes febrile and has seizure recurrence and worsening neurologic symptoms, including cerebral salt wasting and encephalopathy. Subsequent neuroimaging demonstrates cerebral edema and diffuse brain injury. A high index of suspicion for a rare condition ultimately leads us to perform the specialized testing that confirms the diagnosis. We will discuss the diagnostic challenges that arise from an atypical presentation of an uncommon condition, and from the disease progression that is modified by previous interventions.
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