Format

Send to

Choose Destination
See comment in PubMed Commons below
Acta Neuropathol. 2004 Nov;108(5):379-85. Epub 2004 Sep 4.

Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

Author information

1
Department of Neurology, University of Texas Southwestern Medical School, 5323 Harry Hines Blvd., Dallas, TX 75390-9129, USA. Anne.Lipton@UTSouthwestern.edu.

Abstract

This report presents the largest series of consecutive, neuropathologically confirmed cases of frontotemporal degeneration (FTD). Prior studies have found dementia lacking distinctive histology (DLDH) to be the most common pathology underlying the clinical diagnosis of FTD. In this series of 76 cases, 29 (38%) were found to have frontotemporal lobar degeneration with motor neuron disease-type inclusions (FTLD-MND-type) or FTLD-MND (with ALS), the most common neuropathological classification in our series. Only eight (11%) were classified as Pick's disease. Several cases originally designated as DLDH could be reclassified as FTLD-MND-type based on current recommendations for classification of FTD.

PMID:
15351890
DOI:
10.1007/s00401-004-0900-9
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Springer
    Loading ...
    Support Center