An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease

Seishi Terada, Hideki Ishizu, Osamu Yokota, Takeshi Ishihara, Hanae Nakashima, Aki Kugo, Yuji Tanaka, Tadao Nakashima, Yoshihiko Nakashima, Shigetoshi Kuroda

Research output: Contribution to journalArticle

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Abstract

We report here a case of orthochromatic leukodystrophy with spheroids. A 40-year-old woman developed forgetfulness. About 1-year after the onset, clinical examination confirmed global intellectual deterioration with amnesia, spatiotemporal disorientation, and impairment of judgment. At age 43, she experienced tonic-clonic convulsions several times, and died of pneumonia at the age of 44. Alzheimer's disease was suspected clinically. Pathologically, there was severe diffuse demyelination of the deep white matter of the frontal, parietal and occipital lobes with relative preservation of the subcortical U fibers. In the central demyelinated areas, myelin loss was severe with diffuse gliosis, moderate loss of axons, and many axonal spheroids. At the periphery of the severely degenerated regions, there were a lot of macrophages and most had non-metachromatic lipid granules. The cerebral cortex was intact. The neuropathological findings of this case are consistent with hereditary diffuse leukoencephalopathy with spheroids (HDLS). Ten cases of HDLS were reviewed and presented many findings in common. The gray matter was intact and U fibers were well preserved in most cases. In white matter lesions, severe loss of myelin, moderate to severe axonal loss, much axonal swelling, and the presence of macrophages and hypertrophic astrocytes were common findings. In some cases with HDLS, dementia appeared without obvious neurological manifestations in the early stage. We should remember that some cases with HDLS show clinical symptoms similar to Alzheimer's disease, especially in the early stage.

Original languageEnglish
Pages (from-to)538-545
Number of pages8
JournalActa Neuropathologica
Volume108
Issue number6
DOIs
Publication statusPublished - Dec 2004

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Autopsy
Alzheimer Disease
Myelin Sheath
Macrophages
Tonic-Clonic Epilepsy
Occipital Lobe
Confusion
Parietal Lobe
Gliosis
Amnesia
Frontal Lobe
Demyelinating Diseases
Neurologic Manifestations
Astrocytes
Cerebral Cortex
Axons
Dementia
Pneumonia
Lipids
Hereditary Diffuse Leukoencephalopathy with Spheroids

Keywords

  • Alzheimer's disease
  • Forgetfulness
  • Hereditary diffuse leukoencephalopathy with spheroids
  • Leukodystrophy
  • Orthochromatic leukodystrophy

ASJC Scopus subject areas

  • Clinical Neurology
  • Pathology and Forensic Medicine
  • Neuroscience(all)

Cite this

An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease. / Terada, Seishi; Ishizu, Hideki; Yokota, Osamu; Ishihara, Takeshi; Nakashima, Hanae; Kugo, Aki; Tanaka, Yuji; Nakashima, Tadao; Nakashima, Yoshihiko; Kuroda, Shigetoshi.

In: Acta Neuropathologica, Vol. 108, No. 6, 12.2004, p. 538-545.

Research output: Contribution to journalArticle

Terada, S, Ishizu, H, Yokota, O, Ishihara, T, Nakashima, H, Kugo, A, Tanaka, Y, Nakashima, T, Nakashima, Y & Kuroda, S 2004, 'An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease', Acta Neuropathologica, vol. 108, no. 6, pp. 538-545. https://doi.org/10.1007/s00401-004-0920-5
Terada, Seishi ; Ishizu, Hideki ; Yokota, Osamu ; Ishihara, Takeshi ; Nakashima, Hanae ; Kugo, Aki ; Tanaka, Yuji ; Nakashima, Tadao ; Nakashima, Yoshihiko ; Kuroda, Shigetoshi. / An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease. In: Acta Neuropathologica. 2004 ; Vol. 108, No. 6. pp. 538-545.
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