Immunohistochemical properties of ocular adenomas, adenocarcinomas and medulloepitheliomas

Ocular medulloepitheliomas, adenomas and adenocarcinomas share a common phenotype and originate from the optic cup neuroectoderm. This can make it very difficult to differentiate between these tumors histopathologically. Therefore, this study focused on identifying a combination of immunologic marke...

Full description

Saved in:
Bibliographic Details
Published inVeterinary ophthalmology Vol. 9; no. 6; pp. 387 - 394
Main Authors Klosterman, E, Colitz, C.M.H, Chandler, H.L, Kusewitt, D.F, Saville, W.J.A, Dubielzig, R.R
Format Journal Article
LanguageEnglish
Published Malden, USA Malden, USA : Blackwell Publishing Inc 01.11.2006
Blackwell Publishing Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Ocular medulloepitheliomas, adenomas and adenocarcinomas share a common phenotype and originate from the optic cup neuroectoderm. This can make it very difficult to differentiate between these tumors histopathologically. Therefore, this study focused on identifying a combination of immunologic markers that might be used in the diagnosis of these tumors. These markers included AE1/AE3, CK7, CK20, and telomerase reverse transcriptase (TERT). Routine immunohistochemical staining was performed on 27 whole globes diagnosed with one of these tumors. The tumors that immunostained for TERT showed increasing immunoreactivity as the tumor types increased in aggressiveness. None of the tumor types were immunopositive for CK7. CK20 immunostaining was found in the adenomas but not in the adenocarcinomas or medulloepitheliomas. AE1/AE3 expression was present more consistently in the adenocarcinomas and less frequently in the adenomas. AE1/AE3 expression was present in only one of six medulloepitheliomas. Furthermore, CK20 and TERT showed inverse expression patterns, i.e. TERT increased in expression and CK20 decreased in expression with increasing aggressiveness. These results may be important diagnostic and prognostic indicators for these tumors.
Bibliography:http://dx.doi.org/10.1111/j.1463-5224.2006.00478.x
ArticleID:VOP478
istex:7330915292D0F254215CD6EE8DFCBA53D99981C0
ark:/67375/WNG-HHSBF7K0-7
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1463-5216
1463-5224
DOI:10.1111/j.1463-5224.2006.00478.x