Description

Certain histologic features of squamous cell carcinoma arising in the oropharynx can be combined to give a score which characterizes the tumor. A somewhat similar score termed the histologic malignancy score (HMS) by Woolgar et al is described in the next section.


 

Parameters:

(1) degree of keratinization

(2) nuclear differentiation

(3) mitotic rate

(4) inflammatory response

(5) vascular and/or lymphatic invasion

(6) pattern of invasion

 

Histologic Parameter

Finding

Points

cytoplasmic keratinization

highly degree, with well-formed pearls

1

 

moderate, 20-50% of the cells, attempts at pearl formation

2

 

poor, 5-20% of the cells with suggestion of keratinization

3

 

no evidence of keratinization

4

nuclear differentiation

few enlarged nuclei, > 75% mature appearing

1

 

50-75% mature appearing nuclei

2

 

considerable nuclear pleomorphism, 25% mature appearing

3

 

anaplastic tumor

4

mitoses, average number per high power field

0-1

1

 

2-3

2

 

4-5

3

 

> 5

4

inflammatory (lymphoplasmacytic) response

continuous rim

1

 

patchy rim

2

 

occasional patch

3

 

none

4

vascular/lymphatic invasion

not identified

1

 

not identified

2

 

not identified

3

 

identified

4

pattern of invasion

pushing border

1

 

solid cords

2

 

thin irregular cords

3

 

single cells

4

 

where:

• The scoring of vascular-lymphatic invasion when it is "not identified" is confusing to me. The score of Jakobsson et al used responses none, possible, few, and numerous. I have used the latter in the spreadsheet.

 

total histologic score =

= (points for keratinization) + (points for nuclear differentiation) + (points for mitotic activity) + (points for inflammatory response)+ (points for vascular/lymphatic invasion pattern) + (points for invasion pattern)

 

Interpretation:

• minimum score: 6

• maximum score: 24

• The total score did not demonstrate prognostic value, but certain elements did.

 

Prognostic significance of elements:

• The pattern of invasion: for pushing margin (1) and solid cords, the 5 year survival (from Figure 6, page 2999, Crissman) was 62.5%; for thin, irregular cords (3) and single cells (4) it was 25%.

• If clinical parameters (tumor size, clinical node status, sex and age) were not included, then the mitotic rate became significant in predicting the patient survival rate.

• In T2 and T3 tumors, the mitotic rate and pattern of invasion were important in predicting which patients would die of their disease., while the presence of tumor in vascular spaces was a predictor of survival.

 


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