Familial dementia due to adult polyglucosan body disease

E. H. Bigio, M. F. Weiner, F. J. Bonte, C. L. White

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Background: Adult polyglucosan body disease (APBD) is a rare disorder, presenting with varying combinations and severity of upper and lower motor neuron dysfunction, sensory deficits, dementia, and urinary incontinence. Onset is in the 40s or 50s. The diagnosis is made by finding polyglucosan bodies (PB) in histologic sections of brain or spinal cord, peripheral nerve, or dermal sweat glands. Although 2 pairs of the 22 previously reported cases were siblings, the familial nature of the disease has not been emphasized. Methods: We report 2 adult siblings, a male and a female, each of whom had the clinical diagnosis of vascular dementia. Both were confirmed at autopsy to have APBD. We characterized the lesions in autopsy tissues using a battery of histological stains, lectin histochemistry, and electron microscopy. Results: Innumerable PB were distributed throughout brain, heart, skeletal muscle, liver, and dermal sweat glands. PB were highlighted by periodic acid Schiff stain and concanavalin A lectin. Ultrastructurally, PB were composed of aggregates of filaments within axons and astrocytic processes, and lying free in the neuropil, but not within neuronal perikarya. Conclusions: It is important to consider APBD in cases of familial dementia of unknown etiology. Ante-mortem biopsy of axillary skin may be diagnostic.

Original languageEnglish (US)
Pages (from-to)227-234
Number of pages8
JournalClinical Neuropathology
Volume16
Issue number4
StatePublished - Jul 1997

Fingerprint

Dementia
Sweat Glands
Lectins
Skin
Siblings
Autopsy
Coloring Agents
Vascular Dementia
Periodic Acid
Neuropil
Brain
Urinary Incontinence
Motor Neurons
Concanavalin A
Peripheral Nerves
Axons
Spinal Cord
Myocardium
Electron Microscopy
Skeletal Muscle

Keywords

  • Adult polyglucosan body disease
  • Carbohydrate metabolism
  • Dementia
  • Hereditary diseases
  • Lafora disease
  • Metabolic diseases
  • Polyglucosan bodies

ASJC Scopus subject areas

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

Cite this

Bigio, E. H., Weiner, M. F., Bonte, F. J., & White, C. L. (1997). Familial dementia due to adult polyglucosan body disease. Clinical Neuropathology, 16(4), 227-234.

Familial dementia due to adult polyglucosan body disease. / Bigio, E. H.; Weiner, M. F.; Bonte, F. J.; White, C. L.

In: Clinical Neuropathology, Vol. 16, No. 4, 07.1997, p. 227-234.

Research output: Contribution to journalArticle

Bigio, EH, Weiner, MF, Bonte, FJ & White, CL 1997, 'Familial dementia due to adult polyglucosan body disease', Clinical Neuropathology, vol. 16, no. 4, pp. 227-234.
Bigio, E. H. ; Weiner, M. F. ; Bonte, F. J. ; White, C. L. / Familial dementia due to adult polyglucosan body disease. In: Clinical Neuropathology. 1997 ; Vol. 16, No. 4. pp. 227-234.
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