Pathological and biochemical studies on a case of Pick disease with severe white matter atrophy

Kazuo Yamakawa1, Masashi Takanashi, Masao Watanabe

  • 1Department of Neurology, Juntendo Urayasu Hospital, Chiba, Japan.

Insights

This study details a rare case of Pick disease with early and severe frontal lobe white matter atrophy. Findings suggest both white matter myelinated fibers and neurons are primary targets in Pick disease.

Area of Science:

  • Neurology
  • Neuroscience
  • Pathology

Background:

  • Pick disease is a rare neurodegenerative disorder.
  • It typically affects the frontal and temporal lobes, leading to cognitive and behavioral changes.

Observation:

  • A male patient with Pick disease presented with early-onset apathy and severe frontal lobe white matter atrophy.
  • MRI scans revealed significant cortical and white matter atrophy in the frontal lobe.
  • Autopsy confirmed severe atrophy in frontal and temporal lobes, white matter loss, ventricular dilatation, and cortical thinning.

Findings:

  • Histopathology showed extensive loss of myelinated fibers in the frontal white matter.
  • Severe neuronal loss and gliosis were observed in the frontal and temporal cortices.
  • Numerous Pick bodies were present, characteristic of the disease.

Implications:

  • This case highlights a rare presentation of Pick disease with predominant frontal lobe and early white matter involvement.
  • The findings suggest that Pick disease may primarily affect both cerebral neurons and white matter myelinated fibers.