Dementia lacking distinctive histology (DLDH) revisited

Ian R A Mackenzie, Jing Shi, Catherine L. Shaw, Daniel DuPlessis, David Neary, Julie S. Snowden, David M A Mann, Daniel Du Plessis

Research output: Contribution to journalArticlepeer-review

Abstract

Although immunohistochemistry has helped to classify the histology of frontotemporal lobar degeneration (FTLD), there have been many cases, described in the literature as showing "dementia lacking distinctive histology" (DLDH), in which this technique has failed to disclose signature pathological changes. Using an automated procedure we have repeated immunostaining for ubiquitin protein (UBQ) in 41 patients with FTLD, 25 of whom were previously considered, on the basis of UBQ immunostaining performed in Manchester, UK, to show FTLD-ubiquitin (FTLD-U) histology and 16 described as DLDH. Both the quality and amount of UBQ immunoreactive (UBQ-ir) pathology (neurites and intraneuronal cytoplasmic inclusions) was significantly increased using the newer staining method. Although the original histological diagnosis was confirmed in the 25 cases previously classified as FTLD-U, the median UBQ score for slides stained in Vancouver increased significantly compared to those stained in Manchester. More importantly, however, some degree of UBQ-ir changes was now disclosed in 13 of the 16 cases previously classified as DLDH and these were now classed as definite or probable FTLD-U. Of the remaining three DLDH cases, clinical diagnostic uncertainties could have explained the lack of specific pathology in two instances. Hence, we conclude that DLDH is a very rare disorder, and that lack of sensitivity for UBQ immunostaining is likely responsible for the failure to disclose this pathology and to provide a diagnosis of FTLD-U. © Springer-Verlag 2006.
Original languageEnglish
Pages (from-to)551-559
Number of pages8
JournalActa Neuropathologica
Volume112
Issue number5
DOIs
Publication statusPublished - Nov 2006

Fingerprint

Dive into the research topics of 'Dementia lacking distinctive histology (DLDH) revisited'. Together they form a unique fingerprint.

Cite this