KI67 EXPRESSION IN LICHEN-SCLEROSUS OF VULVA IN PATIENTS WITH AND WITHOUT ASSOCIATED SQUAMOUS-CELL CARCINOMA

Citation
J. Scurry et al., KI67 EXPRESSION IN LICHEN-SCLEROSUS OF VULVA IN PATIENTS WITH AND WITHOUT ASSOCIATED SQUAMOUS-CELL CARCINOMA, Histopathology, 32(5), 1998, pp. 399-404
Citations number
8
Categorie Soggetti
Cell Biology",Pathology
Journal title
ISSN journal
03090167
Volume
32
Issue
5
Year of publication
1998
Pages
399 - 404
Database
ISI
SICI code
0309-0167(1998)32:5<399:KEILOV>2.0.ZU;2-Y
Abstract
Aims: To investigate the malignant potential of lichen sclerosus, a st udy using the cell proliferation marker Ki67 comparing lichen sclerosu s with and without associated squamous cell carcinoma was performed, M ethods and results: Formalin-fixed, paraffin-embedded slides of 13 cas es of lichen sclerosus with associated carcinoma, and 31 cases without associated carcinoma, including 16 random cases, seven with epidermal thickening and eight with epidermal thinning, were examined by the im munoperoxidase technique for Ki67, a cell proliferation marker. Ki67 r eactivity was mostly seen in the basal and parabasal cells in both gro ups of lichen sclerosus and this pattern was similar to normal skin. s quamous cell hyperplasia and analogous to that of one form of squamous cell carcinoma. There was a mean of 50 Ki67 positive cells per 100 ba sal cells in lichen sclerosus with associated squamous cell carcinoma; however, in squamous cell hyperplasia adjacent to carcinoma this rose to 90 Ki67 positive cells per 100 basal cells. In lichen sclerosus wi thout associated carcinoma, the random cases had a count of 53 per 100 basal cells, those with epidermal thickening 53 and those with thinni ng 42. Non-genital normal skin had a count of 71 per 100 basal cells. Conclusion: The lack of qualitative differences of Ki67 expression in normal skin, in lichen sclerosus with and without carcinoma, in squamo us cell hyperplasia and in one form of squamous cell carcinoma indicat es that these conditions share a common localized pattern of cell prol iferation and does not support or deny the malignant potential of lich en sclerosus, The higher Ki67 count in squamous cell hyperplasia adjac ent to carcinoma could indicate premalignancy or a reaction to the car cinoma. In patients without carcinoma, the higher Ki67 count in thicke ned lichen sclerosus compared to thinned suggests that some or all of the cases of thickened lichen sclerosus were lichen sclerosus with squ amous cell hyperplasia or that lichen simplex chronicus superimposed o n lichen sclerosus has a higher Ki67 expression or that the distinctio n between squamous cell hyperplasia and lichen simplex chronicus is on ly one of terminology.