Professional Documents
Culture Documents
2 August 1999
ORAL SURGERY
ORAL MEDICINE
ORAL PATHOLOGY
Objective. The purpose of this study was to clarify characteristic sonomorphologic features of parotid lesions statistically and
to propose new criteria for the differential diagnosis.
Study design. Eighty-six tumorous lesions were analyzed with regard to the following sonomorphologic features: boundary,
shape, echo intensity level, distribution of internal echoes, and acoustic enhancement. Stepwise polychotomous logistic
regression analysis was performed to assess characteristic sonographic features. As dependent variables, we used pleomorphic
adenoma, Warthin tumor, malignant tumors and other benign lesions; as predictor variables, we used the aforementioned sonomorphologic features. Proportion of the occurrence of each dependent variable was calculated.
Results. Lobular shape and homogeneous internal echoes predicted pleomorphic adenoma. A lesion with multiple anechoic
areas would be Warthin tumor with very high sensitivity. Malignant tumors showed either heterogeneous internal echoes
without characteristic structures or polygonal shape.
Conclusions. These sonomorphologic features should be observed to make more exact differential diagnoses for operation
and therapy planning.
(Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999;88:226-33)
Many kinds of imaging techniques have been developed for diagnosing salivary gland diseases, including
plain radiography, sialography, scintigraphy, computed
tomography (CT), CT-sialography, magnetic resonance
imaging (MRI), and ultrasonography. In recent years,
ultrasonography has become one of the most important
imaging techniques because of its ease of use and
absence of ionizing radiation. Ultrasonography, when
This work was supported in part by DAAD (Deutscher
Akademischer Austausch-dienst) and carried out at University
Hospital Eppendorf, Hamburg University.
aInstructor, Department of Oral & Maxillofacial Radiology, Faculty
of Dentistry, Kyushu University.
bPrivatdozent and Oberarzt, Ear-Nose-Throat Clinic, University
Hospital Eppendorf, Hamburg University.
cProfessor and Chairman, Ear-Nose-Throat Clinic, Siloah Hospital.
dProfessor and Chairman, Department of Oral Pathology, Institute
for Pathology, Hamburg University.
eInstructor, Department of Medical Information Science, Faculty of
Medicine, Kyushu University.
Received for publication Nov 2, 1998; returned for revision Dec 19,
1998; accepted for publication Feb 27, 1999.
Copyright 1999 by Mosby, Inc.
1079-2104/99/$8.00 + 0 7/16/99050
226
Shimizu et al 227
Classes
Boundary
Very clear
Relatively clear
Partially unclear
Oval
Lobular
Polygonal
Glandular parenchymal
slightly hypoechoic
Very hypoechoic
Homogeneous
Multiple anechoic areas
Heterogeneous with characteristic structures
Heterogeneous without characteristic structures
Enhanced
Unchanged
Attenuated
Shape
Acoustic enhancement
(posterior echoes)
No. of cases
72
22
30
20
4
2
4
5
5
1
1
1
2
14
2
2
2
1
1
2
4
Sonographic features
Before surgical intervention, ultrasonography was
performed with a linear small-parts electronic sonographic scanner (7.5 MHz center frequency; Quantum
2000, Siemens, Erlangen, Germany). Both transversal
and longitudinal scan sections were obtained at the
greatest dimensions of the lesions. The contralateral
(normal) parotid glands were also examined.
Sonographic features of the lesions are listed in Table
I. With regard to boundaries, if a lesion had either a
thin hyperechoic line on the anterior side or a capsulelike structure, it was categorized as very clear. If a
contour showed any interruption, it was classified as
partially unclear. For echo intensity level, if a lesion
showed approximately the same echo intensity level as
glandular parenchyma, it was termed glandular
parenchymal level. If anechoic areas in a lesion
accounted for less than 50% of the lesion, it was categorized as slightly hypoechoic; if more than 50%, as
very hypoechoic. For the distribution of internal
echoes, we categorized multiple anechoic areas as a
specific class. We categorized other characteristic findings of internal echoes, such as a hilus and regularly
distributed hyperechoic lines, as heterogeneous with
characteristic structures. Acoustic enhancement was
228 Shimizu et al
Statistical methods
Stepwise polychotomous logistic regression analysis
was performed to assess characteristic sonographic features of the various parotid diseases to determine which
could be used as the criteria for sonographic differential
diagnoses. We used a BMDP PR module (BMDP Statistical Software Inc, Los Angeles, Calif) for data analysis.
The dependent variable, Y, had 4 groups: pleomorphic
adenoma (Pleo), Warthin tumor (Warth), malignant
tumors (Malig), and other benign lesions (Others).
As candidates for independent (predictor) variables, we
used the 5 features on sonograms listed in Table I:
boundary, shape, echo intensity level, distribution of
internal echoes, and acoustic enhancement. Categories of
independent variables were also made on the basis of the
classes in Table I. The design variables were generated
from independent variables by means of the partial
method in the BMDP PR. The reference categories for
the 5 variables were very clear, oval, glandular
parenchymal slightly hypoechoic, homogeneous, and
enhanced, respectively. Therefore, the exponentiated
value of the coefficient for each category could be
considered an odds ratio to the reference category.
We analyzed 78 cases for this statistical analysis. We
excluded 2 cases that could be diagnosed as malignant
tumors only by attenuated posterior echoes (including
internal shadow)15 and another 6 cases whose shape or
enhancement we could not estimate.
Shimizu et al 229
p(Y) =
uY =
Pleo
b Pleo
XO + b shape(oval) +
Pleo (homogeneous).
b distribution
To select an effective set of predictors for differential diagnoses from the 5 variables, stepwise analysis
was performed as a forward-stepping procedure with
a P value of less than .05 for variable inclusion and
greater than .06 by likelihood ratio test for exclusion
from the model.
RESULTS
Histopathologic diagnoses of the lesions
Table II contains the histopathologic results for
the lesions. There were 72 cases of benign lesions,
58 of which were benign tumors (67.4% of all lesions).
Most were pleomorphic adenomas (22 cases, 37.9% of
benign tumors, 25.6% of all lesions) or Warthin tumors
(30 cases, 51.7% of benign tumors, 34.9% of all
lesions). Figs 1 and 2 are representative cases of pleomorphic adenoma and Warthin tumor, respectively.
Four cases of lipoma and 2 cases of basal cell adenoma
were also seen as benign tumors. We had 14 cases of
various malignant tumors (16.3% of all lesions; Fig 3).
For the other benign lesions, 4 cases of cyst and 5 cases
of lymphadenitis were observed.
Sonomorphology of the tumorous lesions
Table III contains the sonomorphologic results for
the tumorous lesions. Pleomorphic adenoma showed
relatively clear boundaries in 17 (77.3%) of 22 cases,
Statistical analysis
In the final logistic regression model, 2 variables
were selected as independent variables: distribution of
internal echoes and shape (P < .0001 and P = .0007 for
likelihood ratio test, respectively). The BMDP PR
module provided coefficient, standard error (SE), coefficient/SE, odds ratio, and 95% confidence interval to
reference category for each independent variable. Table
IV contains coefficient and SE for pleomorphic
adenomas, Warthin tumors, and malignant tumors.
Though SE for some independent variables showed
very wide range because of the small number of cases,
the P value was less than .05 by likelihood ratio test.
230 Shimizu et al
Very
clear
Boundaries
Relatively
clear
Partially
unclear
Oval
5
21
17
8
2
19
3
1
3
4
3
2
42
1
1
1
1
2
5
36
7
8
1
1
3
5
1
2
34
Lobular
Polygonal
Unable
to
classify
20
8
3
1
1
3
7
43
4
6
1
1
3
Hetero 1, Heterogeneous with characteristic structures; Hetero 2, heterogeneous without characteristic structures.
Pleo
b Pleo
XO + bshape(lobular) +
Pleo
b distribution
(multiple anechoic areas) =
-0.1612 + 1.870 + (-19.75),
uWarth =
uMalig =
-0.5108 + 0 + (-25.67),
0.869,
p(Malig) <
0.001,
DISCUSSION
Ultrasonography has become the preferred diagnostic
method for tumorous lesions in the salivary glands. If we
could diagnose lesions precisely by means of ultrasonography, it would be of great value for treatment and operation planning. Inasmuch as there are many kinds of tumorous lesions, especially in parotid glands, and some of
them show characteristic sonomorphology, it should be
possible to make reliable diagnostic criteria for parotid
tumorous lesions. Although many authors1-5,7-15 have
reported ultrasonic differential diagnoses for the salivary
gland diseases, their criteria have not been used widely,
because the diagnoses were made empirically in the
authors own hospitals and are not uniform. Complexes
of characteristic findings of some representative diseases
were stated, and sensitivity, specificity, and accuracy in
each disease were calculated; however, because no statistical analyses were performed, the most important factors
for differential diagnoses have remained obscure. Therefore, we performed a statistical study to clarify which
sonographic features should be emphasized in the criteria
for differential diagnoses of parotid tumorous lesions.
We used 5 sonographic features (Table I): boundary,
shape, echo intensity level, distribution of internal
echoes, and acoustic enhancement.1,4 Other authors
have used only the first 4 of these features.7,8,11 However,
because attenuated posterior echoes in acoustic
enhancement have been stated to be one of the malignant signs,3,15 we used the former series of features.
Sonomorphologic features of pleomorphic adenoma
were reported in the literature as follows: clear
boundary,3,7,10 lobulated shape,1 slightly hypoechoic
echo intensity level,1,7,10 homogeneous internal
echoes,3,7,8,10,11 and enhanced posterior echoes.3,7,11
Because lobular shape was a main characteristic
feature of pleomorphic adenoma (Table V) and is also
listed among the histopathologic features of pleomor-
Shimizu et al 231
Acoustic enhancement
Unable
to
classify
20
12
2
18
20
2
28
16
11
4
19
4
2
1
3
2
12
56
3
2
3
2
30
1
3
1
4
31
30
4
1
1
4
3
4
19
6
6
3
2
2
5
40
2
2
1
3
3
7
41
2
2
232 Shimizu et al
Independent variables
Distribution of internal echoes
Homogeneous
Multiple anechoic areas
Hetero 1
Hetero 2
Shape
Oval
Lobular
Polygonal
Constant
Dependent variables
Warthin tumors
Coef
SE
Pleomorphic adenomas
Coef
SE
0
19.75
2.894
1.017
0
1.870
6.121
0.1612
0
4590
0.958
1.660 l05
0
2.932
20.78
1.265
0
0.943
385
0.901
0
0.9848
8.331
0.0510
Malignant tumors
Coef
SE
0
1.06
7420.
1.560 l05
0
25.67
1.887
26.12
0
1.02
117
0.851
0
0
19.84
0.5108
0
2790.
1.27
1.270 l05
0
0
191
0.730
Lobular
Oval
Lobular
Polygonal
Oval
Lobular
Polygonal
Polygonal
Polygonal
Oval
Oval
Lobular
Totals
Homogeneous
Multiple anechoic areas
Multiple anechoic areas
Multiple anechoic areas
Hetero 2
Hetero 2
Homogeneous
Hetero 1
Hetero 2
Homogeneous
Hetero 1
Hetero 1
4.7
94.7
86.9
100.0
0.0
0.0
0.0
0.0
0.0
27.9
0.0
0.0
8.0
0.0
0.0
0.0
100.0
100.0
100.0
100.0
100.0
17.6
8.0
6.5
13.4
5.3
13.1
0.0
0.0
0.0
0.0
0.0
0.0
29.4
87.9
71.6
1
18*
7*
2*
0
0
0
0
0
1
0
0
29
3
0
0
0
1*
2*
1*
3*
0*
0
0
1
11
2
1
1
0
0
0
0
0
0
3*
6*
5*
18
22
19
8
2
1
2
1
3
0
6
6
8
78
Pleo, Pleomorphic adenoma; Warth, Warthin tumor; Malig, malignant tumors; Others, other benign lesions.
*Case predicted correctly.
Shimizu et al 233
Table VI. Sensitivity, specificity, accuracy, and true positive rates for dependent variables
Dependent variables
Sensitivity
Specificity
Accuracy
Pleomorphic adenoma
80.0 (16/20)
0.557-0.965
93.1 (27/29)
0.758-1.019
63.6 (7/11)
0.306-0.966
77.8 (14/18)
0.519-0.959
93.1 (54/58)
0.824-0.991
95.9 (47/49)
0.848-1.012
100 (67/67)
0.932-1.023
90.6 (58/64)
0.800-0.971
89.7 (70/78)
0.802-0.959
94.9 (74/78)
0.867-0.994
94.9 (74/78)
0.867-0.994
92.3 (72/78)
0.834-0.977
72.7 (16/22)
0.495-0.907
93.1 (27/29)
0.758-1.019
100 (7/7)
0.561-1.150
70.0 (14/20)
0.474-0.926
Warthin tumor
Malignant tumors
Other benign lesions
*Percentage (no. of cases); 95% confidence intervals (lower and upper limits).
6.
7.
8.
9.
10.
11.
12.
13.
14.
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Reprint requests:
M. Shimizu, DDS, PhD
Department of Oral & Maxillofacial Radiology
Faculty of Dentistry, Kyushu University
Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582
Japan