An autopsy case of progressive multifocal leukoencephalopathy with massive iron deposition in juxtacortical lesions

Kosuke Okamoto1, Akitoshi Takeda1, Hiroyuki Hatsuta1,2,3

  • 1Department of Neurology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Insights

This study reports a rare case of progressive multifocal leukoencephalopathy (PML) in a lymphoma patient with significant iron deposits. The findings highlight iron deposition as a potential feature in PML, observed both via imaging and autopsy.

Area of Science:

  • Neuroscience
  • Neuropathology
  • Oncology

Background:

  • Progressive multifocal leukoencephalopathy (PML) is a serious demyelinating disease caused by JC virus.
  • Iron deposits in PML are not well-documented.
  • Follicular lymphoma treatment can sometimes lead to opportunistic infections like PML.

Observation:

  • A 71-year-old woman with follicular lymphoma developed PML after chemotherapy (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisolone).
  • She presented with visual disturbances and aphasia.
  • MRI revealed white matter lesions with substantial juxtacortical iron deposition.

Findings:

  • JC virus PCR confirmed PML diagnosis.
  • Autopsy showed demyelination and abundant hemosiderin-laden macrophages and ferritin-containing reactive astrocytes in juxtacortical regions.
  • This case demonstrates significant iron deposition in PML, confirmed radiologically and pathologically.

Implications:

  • This case expands the understanding of PML pathology, particularly concerning iron accumulation.
  • It suggests that iron deposition may be a notable feature in certain PML cases, especially in immunocompromised patients.
  • Further research is warranted to explore the role and mechanisms of iron deposition in PML pathogenesis.

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