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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.
Abstract:
We report on a male patient with Pick disease who had shown severe white matter atrophy and dilatation of the lateral ventricle in the frontal lobe from an early stage. Upon admission to our hospital 2 years after disease onset, the patient showed apathy, and MRI revealed severe atrophy of the cortex and white matter of the frontal lobe. He died at age 74, 11 years after disease onset. Autopsy revealed severe atrophy of the frontal and temporal lobes, severe loss of white matter in the frontal lobe, dilatation of the lateral ventricles, and cortical thinning. Histopathological examination showed severe loss of myelinated fibers in the frontal white matter and severe neuronal loss with gliosis in the frontal and temporal cortices. Many Pick bodies were seen. Our patient had a rare case of Pick disease predominantly affecting the frontal lobe with severe involvement of the white matter from an early stage. This case suggests that myelinated fibers in the white matter as well as cerebral neurons are primarily affected in Pick disease.
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.
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