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Published on: November 20, 2015
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
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.
Abstract:
We report the case of a female Japanese infant who was diagnosed with incontinentia pigmenti (IP) on the basis of the clinical and pathological findings of characteristic skin lesions and the detection of deletion in the nuclear factor-kappa B essential modulator gene at Xq28. The patient developed repetitive seizures at the age of 7 months when she was diagnosed with acute disseminated encephalomyelitis (ADEM), an inflammatory demyelinating disease of the central nervous system that often occurs after vaccination or infection. The causative infectious agent in this patient seemed to be Mycoplasma pneumoniae because of the increased titer of its serum antibody and the detection of its DNA in the initial cerebrospinal fluid sample. This patient showed significant improvement on receiving immunosuppressive therapy with corticosteroids. This is the second case report presenting an IP patient susceptible to ADEM, and therefore, ADEM should be considered early in the differential diagnosis of acute neurological illness for IP patients.
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