Radiological manifestation of familial acute necrotizing encephalopathy with RANBP2 mutation in a Far-East Asian family: Case report

Medicine (Baltimore). 2021 Mar 26;100(12):e25171. doi: 10.1097/MD.0000000000025171.

Abstract

Rationale: Acute necrotizing encephalopathy (ANE) is a specific type of encephalopathy usually followed by febrile infection. It has an aggressive clinical course; however, it usually does not recur after recovery in cases of spontaneous ANE. Nevertheless, there are several studies reporting recurrences in familial ANE with RAN-binding protein 2 (RANBP2) mutation. There are few cases of familial ANE with RANBP2 mutation in Asian populations.

Patients concerns: A 21-month-old Korean boy who was previously healthy, presented with seizure following parainfluenza - a virus and bocavirus infection, followed by 2 recurrent seizure episodes and encephalitis after febrile respiratory illnesses. Meanwhile, his 3-year-old sister had focal brain lesions on neuroimaging studies when evaluated for head trauma. The siblings also had an older brother who presented status epilepticus after febrile respiratory illness at the age of 10 months old.

Diagnosis: Brain magnetic resonance imaging was performed to evaluate the seizure and neurologic symptoms. Imaging findings showed variable spectrum - from non-specific diffuse white matter injury pattern to typical "tricolor pattern" of the ANE on diffusion-weighted images. The other 2 siblings showed focal lesions in both external capsules and severe diffuse brain edema. Genetic tests identified a heterozygous missense mutation in the RANBP2 [c.1754C>T (p.Thr585Met)] in 2 siblings and their mother.

Interventions: Patients were treated conservatively with anticonvulsive agents, intravascular immunoglobulin, and steroids.

Outcomes: Among the 3 siblings, 2 male siblings died from familial ANE, whereas the female sibling was asymptomatic.

Lessons: These cases highlight the radiological aspects of familial ANE with incomplete penetrance of the RANBP2 gene in 3 family members, showing variable involvements of the brain and natural history on magnetic resonance images. Radiologists should be aware of the typical and atypical imaging findings of familial ANE for prompt management of affected patients.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Anticonvulsants / therapeutic use
  • Asian People / genetics*
  • Child, Preschool
  • Diffusion Magnetic Resonance Imaging
  • Female
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use
  • Infant
  • Leukoencephalitis, Acute Hemorrhagic / complications
  • Leukoencephalitis, Acute Hemorrhagic / diagnostic imaging*
  • Leukoencephalitis, Acute Hemorrhagic / drug therapy
  • Leukoencephalitis, Acute Hemorrhagic / genetics*
  • Male
  • Molecular Chaperones / genetics*
  • Mutation, Missense*
  • Nuclear Pore Complex Proteins / genetics*
  • Penetrance
  • Seizures / drug therapy
  • Seizures / etiology
  • White Matter / diagnostic imaging
  • Young Adult

Substances

  • Adrenal Cortex Hormones
  • Anticonvulsants
  • Immunoglobulins, Intravenous
  • Molecular Chaperones
  • Nuclear Pore Complex Proteins
  • ran-binding protein 2