Manuscript accepted on :August 05, 2016
Published online on: --
M. K. Masthan, E. Rajesh, U. Tamilarasi and N. Anitha
Department of Oral Pathology, Sree Balaji Dental College and Hospital, Bharath University, Pallikaranai, Chennai-600100.
DOI : https://dx.doi.org/10.13005/bpj/1012
Abstract
Pathologist assess oral precancerous lesions with their dysplastic features by grading of oral epithelial dysplasia (OED) .Evaluating of precancerous lesion arises from two factors (1) lack of knowledge in predicting future development of cancer. (2) Lack of evaluating the criteria which is already established. This article provide a detail review of all the grading systems.
Keywords
epithelial dysplasia; precancerous; photographic
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Introduction
Oral squamous cell carcinoma is a most common changes in the oral mucosa1. leukoplakia is one of the most common potentially malignant disorders2. Dysplasia is reversible. When the stimulus is removed , the dysplastic changes will revert back to normal. When the irritant is removed , epithelium shows cellular atrophy3. It manifest as a cell death or neoplastic transformation. In epithelial dysplasia malignant development is more important than the clinical characteristics2,4.
Grading in dysplasia
Many combinations of dysplastic features are used in grading system and there is difficulty in assessing the various degrees of epithelial dysplasia . To assess the severity of the dysplastic features many grading systems have been proposed . There are various grading systems given by many authors , following are the most commonly used grading systems
Smith and Pindborg’s classification5
1978 WHO classification6
Ljubljana classification squamous intraepithelial lesions (SIL)7,8
2005 WHO classification9
New Binary system10
Smith and Pindborg Classification5
In the year 1969 Smith and Pindborg were first to standardize the grading for epithelial dysplasia . This system was based on the means of the different histological changes and photographic method. In this method standardized photographs are being compared with histologic sections and given 13 histologic features. Now they graded the epithelial dysplasia as absent , marked or slightly and also the score is given. For absent the score was given as zero and for marked or slightly the score was between 1 and 10
1978 WHO Classifi cation6
The “histopathological typing of cancer and precancer lesions ” was given by WHO in the year 1997 . They have given 12 characteristics of the epithelial dysplasia which was graded as mild , moderate and severe according to the characters which are present.
List of Characteristic features are
Loss of polarity of basal cells
An increased nuclear-cytoplasmic ratio
Drop shaped rete pegs
The presence of more than one layer of cells havingthe basaloid appearance
Increased number of mitotic figures
Irregular epithelial stratification
The presence of mitotic figures in the superficial halfof the epithelium
Nuclear hyperchromatism
Cellular polymorphism
Reduction of cellular cohesion
Enlarged nucleoli
Keratinization of single cells or cell groups in the
prickle cell layer
They graded epithelial dysplasia as
Mild
Moderate
Severe
Mild dysplasia
Nuclear abnormality is slight in the basal third of epithelium and it was minimal in the upper layer with cell maturation. Few abnormal mitosis maybe seen accompanied by chronic inflammation.
Moderate dysplasia
Basal 2/3rd of the epithelium shows nuclear abnormalities persisting up to thesurface. Cell maturation and stratification are seen in the upper layer. Mitosis occurs in the Parabasal and intermediate layer.
Severe dysplasia
More than 2/3rd of the epithelium shows nuclearabnormalities and cell maturation is lost. stratification and abnormal mitosis is seen in the superficial layers. Carcinoma in situ was mergedinto severe dysplasia.
Ljubljana Classifi cation SIL
In the year 2003 zeodner proposed criteria for grading hyperplastic epithelial lesions of the oral cavity as simple , atypical and abnormal hyperplasia
Simple hyperplasia
Basal and parabasal layer remains intact without any cellular atypia and thickening of the prickle cell layer is seen.
Abnormal hyperplasia
It shows increase in size from basal layer up to halfof the epithelial thickness. Stratification remains unchanged with moderately enlarged nuclei. Basal cell layer shows mitosis and dyskeratosis is seen less than 5% of the epithelial cells
Atypical hyperplasia (risky epithelium)
Cells of the epithelium are altered showing malignant changes but it is not to form carcinomatous cells . Epithelial stratification remains unchanged and nuclei is enlarged with irregular contour. Mitotic figures is increased upto to the 2/3rd of the epithelium with increasednuclear-cytoplasmic ratio. Civatte bodies and Dyskeratotic cells may be present.
Carcinoma in situ
Stratification is completely lost and mitotic figures are seen all over the epithelium7
2005 WHO Classifi cation9
In the year 2003 WHO classified the oral epithelial dysplasia as Mild, moderate,severe, carcinoma in situ or hyperplasia based on the architectural changes and the presence or severity of cellular atypia according tothe presence and severity of cellular atypia and thearchitectural features. It was issued by WHO in the new book “classification of tumors of the head andneck.”9
Architectural characteristics
Abnormally superficial mitoses
Irregular epithelial stratification
Drop-shaped rete ridges
Keratin pearls within rete pegs
Loss of polarity of basal cells
Increased number of mitotic figures
Cellular characteristics
Anisonucleosis and Anisocytosis
Nuclear and Cellular pleomorphism
Dyskeratosis
Increased number and size of nucleoli
Increased nuclear-cytoplasmic ratio
Atypical mitotic figures
Grading systems of oral epithelial dysplasia
Mild dysplasia
Architectural changes limited only tothe lower third of the epithelium along with the cytological atypia
Moderate dysplasia
Architectural changes is seen extending tothe middle third of the epithelium. Degree of cytologicatypia requires upgradation
Severe dysplasia
Architectural disturbances is seen Greater than 2/3rd of the epithelium and the increasednumber of the cytologic atypia
Carcinoma in situ
Architectural disturbances are seen throughout the full thickness of the epithelium. Abnormal mitosis is seen on the superficial layer with atypical figures
Conclusion
Histopathological assessed severity of oral epithelial dysplasia remains the gold standard for the prediction of malignant transformation of precancerous lesions
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