A long time radiological follow-up of neuronal intranuclear inclusion disease: Two case reports

Medicine (Baltimore). 2018 Dec;97(49):e13544. doi: 10.1097/MD.0000000000013544.

Abstract

Rationale: Neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative disease identified with diffusion-weighted imaging (DWI) high-intensity signal in magnetic resonance imaging (MRI). The disappearance of the abnormal signal is extremely rare.

Patient concerns: We present the 2 cases of patients, both of them were suffering from heterogeneous symptoms. We followed up one of them for 7 years with MRI, the other accepted comprehensive MRI inspections.

Diagnoses: DWI high-intensity signal were observed along the corticomedullary junction in MRI plan scan of heads of 2 patients. For patient 1, the hyperintensities in DWI and fluid-attenuated inversion recovery (FLAIR) images in the occipital lobe disappeared 5 years after onset. Based on the biopsy, patient 1 and 2 were diagnosed as NIID.

Interventions: There have not effective medication and prevention for NIID. Patient 1 and 2 received symptomatic treatment.

Outcomes: Up until now, the patients are alive but the disease is progressing.

Lessons: DWI high-intensity signal is a strong clue for the diagnosis of NIID, but the rare case of the disappearance of it may lead to misdiagnosis.

Publication types

  • Case Reports

MeSH terms

  • Diagnosis, Differential
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Humans
  • Intranuclear Inclusion Bodies / pathology
  • Magnetic Resonance Imaging*
  • Male
  • Middle Aged
  • Neurodegenerative Diseases / diagnostic imaging*
  • Neurodegenerative Diseases / pathology
  • Neurodegenerative Diseases / physiopathology*
  • Neurodegenerative Diseases / therapy
  • Skin / pathology

Supplementary concepts

  • Neuronal intranuclear inclusion disease