Acute disseminated encephalomyelitis in an infant with incontinentia pigmenti

Naoya Matsumoto1, Satoru Takahashi, Naohisa Toriumi

  • 1Department of Pediatrics, Abashiri Kosei Hospital, Abashiri, Hokkaido, Japan. naoya5p@mac.com

Brain & Development
|September 24, 2008
PubMed

Insights

Incontinentia pigmenti (IP) patients may develop acute disseminated encephalomyelitis (ADEM), an inflammatory brain disease. Early ADEM diagnosis is crucial for IP patients experiencing neurological symptoms.

Area of Science:

  • Genetics
  • Neurology
  • Immunology

Background:

  • Incontinentia pigmenti (IP) is a rare genetic disorder affecting skin, hair, nails, and teeth.
  • Neurological complications, including seizures, can occur in IP patients.

Observation:

  • A female Japanese infant with IP presented with repetitive seizures at 7 months.
  • The patient was diagnosed with acute disseminated encephalomyelitis (ADEM), potentially triggered by Mycoplasma pneumoniae infection.

Findings:

  • The IP diagnosis was confirmed by characteristic skin lesions and a genetic deletion in the nuclear factor-kappa B essential modulator gene (NEMO) at Xq28.
  • The patient responded well to immunosuppressive corticosteroid therapy.

Implications:

  • This case highlights the susceptibility of IP patients to ADEM, a serious inflammatory central nervous system condition.
  • ADEM should be considered in the differential diagnosis of acute neurological illness in infants with IP.

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