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1251

Value of MR Imaging in Differentiating Benign from Malignant Soft-Tissue Masses: Study of 95 Lesions

Thomas H. Berquist1 Richard L. Ehman1 Bernard F. King1 Charles G. Hodgrnan1 Duane M. llstrup2

MR imaging has largely replaced CT as the technique of choice for preoperative staging of patients with soft-tissue masses. Whether MR imaging can be used to differentiate benign from malignant masses is controversial. Our experience suggests that MR imaging often can characterize soft-tissue masses accurately. To evaluate this question further, we studied 95 consecutive lesions (50 benign and 45 malignant). Consecutive cases were selected to simulate our clinical practice. Surgical proof was available for all masses except hematomas, for which clinical follow-up confirmed the diagnosis. MR images were interpreted twice by three radiologists. The first review was accomplished without any clinical history and the second review with clinical history. Reviewers were asked to classify the lesion as benign or malignant on the basis of their clinical knowledge and analysis of MR image features (size, lesion margin, signal homogeneity, and neurovascular or bone involvement). Although interpretation varied somewhat because of the experience of the reviewers, the specificity and accuracy of diagnosis averaged 90% for both benign and malignant lesions. Negative predictive value for malignancy averaged 94% among the three reviewers. MR imaging is the technique of choice for identification and characterization of softtissue masses. The nature of the lesion (benign vs malignant) can be determined in the majority of cases. AJR

Received

April 5, 1 990; accepted

June26, 1990. 1 Department

of Diagnostic

Clinic and Mayo Foundation,

after

Radiology,

Rochester,

revision

Section

Foundation,

of Biostatistics, Rochester,

Mayo

MN 55905.

0361-803X/90/1 556-1251 C American Roentgen Ray Society

Clinic

December

1990

MR imaging has become the premier method for identifying and staging softtissue masses of the musculoskeletal system. Although MR imaging is sensitive, many authors have reported that it is not useful in differentiating benign from malignant soft-tissue masses [1-S]. Our experience indicates that certain image features are useful in differentiating benign from malignant lesions. Therefore, we elected to perform a blind study of MR images of benign and malignant soft-tissue masses. Images were obtained and interpreted before biopsy or surgical data were obtained. Ninety-five (SO benign and 45 malignant) consecutive soft-tissue masses were studied to determine the usefulness of MR imaging features in differentiating benign from malignant lesions. Nonneoplastic lesions such as abscess and hematoma were included with benign tumors. The primary goal of this study was to determine the value of morphologic characteristics (e.g., lesion size, margins, signal intensity, and neurovascular involvement) in predicting the nature of soft-tissue masses. We also chose radiologists with different levels of experience with MR imaging to determine what effect experience has on the accuracy of interpretation.

Mayo

MN 55905.

Address reprint requests to T. H. Berquist. 2

155:1251-1255,

Materials

and Mayo

and

Methods

MR examinations biopsies The

were

specific

selected diagnoses

of 95 consecutive for

review.

are given

This in Table

and other lesions that mimic neoplasms.

patients series

with included

soft-tissue 45 malignant

masses and

who had not had 50 benign masses.

masses included hematomas, abscesses, Surgical proof was available in all cases except for

1 . Benign

BERQUIST

1252

TABLE

1: Diagnoses

of 95 Soft-Tissue

ET

AL.

TABLE

Masses

Type of Mass

AJR:155,

2: MR Features

of Soft-Tissue

No. (%)

r:5

Feature

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12 9

Cyst Hematoma Lipoma

8

Hemangioma

5

Desmoid Neuroma

4 4

Abscess

2

Malignant

Size (cm) 5 Margin Well

2 1 i i

aneurysm vein

Total Malignant

Irregular Signal

histiocytoma

0 0 6(13) 39 (87)

1 (2) 10(20) 14(28) 25 (50)

7 (i 5)

22 (44)

1 3 (29)

20 (40)

25 (56)

8 (16)

homogeneous

2 (5) 1 1 (24)

21 (42) i 7 (34)

Inhomogeneous

32 (71)

i 2 (24)

17

Liposarcoma Synovial sarcoma

7 6

Mesenchymal sarcoma Rhabdomyosarcoma

3 3

Chondrosarcoma Leiomyosarcoma Neurofibrosarcoma

2 2 2

the lesions (which were to be defined as smooth, partially well defined, or irregular) and the signal intensity and/or homogeneity (recorded on both Ti - and T2-weighted sequences). Also evaluated were neurovascular encasement or displacement, hemorrhage and/or edema in or around the lesion, and bone involvement. After each of

Fibrosarcoma

1

these features was evaluated,

Epithelioid

1

the lesion

as benign

or malignant

histologic

diagnosis.

Specific

(soft tissue)

sarcoma

Lymphoma Total

45

information

hematomas. In these patients, follow-up and hematomas confirmed the clinical was

not

available

to the

in both

upper

and

lower

with resolution diagnosis. This

the lower extremity: 29 (31 %) in 1 1 (i 2%) around the knee. The upper extremity and trunk. The 71 %) also were in the lower always immediately adjacent to

extremities.

MR images were obtained on either a 0.i5-T resistive system (25 patients) or a 1 .5-T Signa system (70 patients). Both Ti -weighted, 500/20 (TRITE), and T2-weighted, 2000/60, spin-echo (SE) sequences were available for each examination. Only pertinent images were selected for review. All patient data were removed from the

images, and all cases were randomized not

separated)

before

(benign and malignant

were

evaluation.

Images were interpreted blindly in separate sessions by three different radiologists. Two radiologists were fellows in cross-sectional imaging

and in the process

of taking

a 3-month

when they began their participation was

a consultant

imaging. in two

Images different

with

were settings.

5 years

MR

imaging

fellowship

in the study. The third radiologist

of experience

randomized

in musculoskeletal

and reviewed

In the first

part

of the

MR

by each radiologist study,

the

radiologists

were given images to review

without any clinical information or other imaging studies to compare with the MR study. After 3-6 months, the images were put in a different order and given to the interpreters a second

of other

evaluation.

imaging

studies

At this

were

able in only about one-third

time,

made

several recorded

the

clinical

available.

of cases because

technique of choice for soft-tissue The reviewers were instructed

were asked to categorize

and, when

diagnoses

possible,

to provide

a

for benign lesions such as

negative

for accuracy,

predictive

sensitivity,

specificity,

and positive and

values.

reviewers.

The majority of all lesions were in the thigh, 1 7 (1 8%) in the leg, and remainder of the lesions were in the majority of malignant lesions (32/45, extremity. Benign cysts were almost joints

the reviewers

hematoma or abscess were also requested when it was possible to provide one. Data were tabulated for both reviews for each of the three examiners. The final diagnoses (lesions benign vs malignant)

were evaluated posttraumatic of symptoms

for

(n=50)

intensity

Homogeneous Majority of mass

50 fibrous

irregular

Benign

(n=45)

defined

Partially

1

Angiolipoma

Malignant

1990

Masses

Benign

Myxoma Thrombosed Thrombosed Epidermoid

December

history

CT scans

and

results

were

MR imaging

availis the

masses at our institution. to categorize cases according

to

specific criteria. The size and location of each lesion were by each radiologist. Other features included the margins of

Results

For lesion size, as measured on MR images, the average of the three measurements was used. The sizes of lesions are summarized in Table 2. No malignant lesions were less than 3 cm in diameter. On the other hand, 22% of benign lesions were less than 3 cm in diameter. Thirteen percent of malignant lesions were 3-5 cm; 87% were larger than 5 cm. On the surface this may seem important; however, 50% of benign lesions also were larger than 5 cm. Forty-four percent of benign lesions had well-defined or sharp margins (Table 2). Slight irregularity was described in 40% of benign masses. Only eight (1 6%) showed total or nearly complete irregularity of margins. Most of the tumor margin was irregular in 38 malignant lesions (85%). However, sharp margins were noted in seven cases (15%). At least some inhomogeneous signal intensity was noted in 43 malignant lesions (95%) (Table 2). Homogeneous signal intensity was unusual in malignant lesions. Small areas of inhomogeneity were present in 1 2 benign lesions (24%). Neurovascular involvement was not common in either benign or malignant lesions; however, some displacement of neurovascular structures occurred in 32 malignant lesions (71 Three malignant lesions (7%) had neurovascular encasement. This was also observed with desmoid tumors (which are considered benign). Hemorrhage or edema or both %).

AJR:155,

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were

December

present

MR

1990

in 27%

of benign

and

54%

OF

of malignant

SOFT-TISSUE

lesions.

The prevalence of hemorrhage and edema in benign lesions was due to the number of hematomas (9/50) included in this group of patients. Bone involvement was noted with malignant lesions and desmoid tumors. Accuracy of interpretation varied somewhat among the reviewers. There were also differences in diagnostic ability related to the type of lesions (benign vs malignant) and availability of clinical data. The latter was especially important for the less experienced radiologists. Accuracy in predicting whether lesions were benign or malignant ranged from a low of 88% in the less experienced group to 93% for the physician experienced in MR imaging (Table 3). Radiologists were able to predict the histology of the lesions in up to 26% of cases, mostly for benign lesions, when no history was available. When

a history

was

available,

the

two

less

experienced

TABLE Masses

4: Observer

Performance

Benign Sensitivity Specificity Positive

Negative Accuracy Malignant Sensitivity Specificity

predictive

Physician

value

(%)

value (%)

(%) (%) (%)

Positive predictive Negative predictive Accuracy (%) experienced

of Soft-Tissue

No. A

(%) (%) predictive

for Detection

Ob server

Type of Mass/ Statistical Measure

a

changed their diagnoses 1 3% and 19% of the time overall. The more experienced physician changed the diagnosis only once on the basis of historical information. The less experienced physicians predicted the nature of benign lesions 38-40% of the time without clinical data and

1253

MASSES

value (%) value (%)

i

2

3

verage

90 90 92 88 90

82 83 95 83 88

90 96 96 90 93

88 90 94 87 90

90

96

96

94

90 88 92

82 93 95

96 90 96

90 87 94

90

88

93

90

in MR imaging.

reviewers

50-52%

of the time

when

history

was

available.

The

physician

more experienced in MR imaging accurately predicted the nature of a benign lesion in 74% of cases. The reviewers were not successful in predicting the histology of malignant lesions. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy were calculated for benign and malignant lesions (Table 4). The data for malignant lesions are particularly important. The specificity for malignant lesions ranged from 82% to 96%, with a negative predictive value of 92-96% and a positive predictive value of 88-90%.

Discussion An

increasingly

common

indication

for

MR

imaging

is to

determine the presence or absence of musculoskeletal masses. When a mass is found in such an examination, the immediate challenge is to characterize it. Several authors [3, 6-9] have noted that clinical data, especially patient age, lesion location, and duration of symptoms, are helpful in addition to image features for characterizing lesions. Some authors [5, 7, 1 0-i 2] have reported, however, that differentiation of benign and malignant lesions is inconsistent when MR features are used. Manipulation of Ti and T2 relaxation times has not improved specificity [1 , 6].

TABLE

3: Accuracy

in Predicting No. (%) (n

Observer

No. Accuracy

Benign =

Lesions

of Diagnoses

95)

Exact Histology

Changed with History i3 1 ga 1

1

85(90)

i5(16)

2

84 (88)

25 (26)

3b

88 (93)

24 (25)

a Diagnosis interpretation b Physician

and Malignant

less accurate after history was changed. experienced in MA imaging.

in 1 1 % of

patients

when

initial

Our results provide support for using MR imaging to characterize soft-tissue masses. By using traditional radiologic criteria, such as homogeneity and boundary characteristics, experienced and inexperienced observers were able to identify malignant lesions with an average sensitivity of 94% in this series. The negative predictive value of an interpretation that a mass was not malignant also was high (94%). Classic benign and malignant lesion characteristics are illustrated in Figures 1 and 2, respectively. Benign lesions (Fig. 1) tend to be well marginated, have homogeneous signal intensity, and do not encase neurovascular structures or invade bone. Malignant lesions (Fig. 2) generally have irregular margins and inhomogeneous signal and more often encase neurovascular structures and involve bone [3, 6]. The benign lesions that most often were classified incorrectly as malignant in this series were desmoid tumors and necrotic benign neoplasms (neurofibromas). A single hemangioma was considered malignant by one observer (Fig. 3); this was a solid inhomogeneous cavernous hemangioma [13, 1 4]. The difficulty of correctly classifying desmoid tumors is not surprising in view of the infiltrative, locally aggressive nature of the lesions [3, 6]. Many of the benign lesions (ganglionic cysts, lipomas, hemangiomas, neuromas [because of location], and most hematomas) were diagnosed correctly on the basis of imaging features alone [1 3, 15-i 7]. When the MR images were interpreted with knowledge of the clinical findings, the specific histologic diagnosis for benign lesions could be predicted in 38-40% of cases by the inexperienced reviewers and in 74% by the more experienced MR imaging consultant. These percentages are higher than the 24% reported by Kransdorf et al. [18]. The malignant lesion most commonly misclassified as benign was synovial sarcoma. Three of the six synovial sarcomas in this group of lesions had smooth margins and a cystic appearance or mimicked hematomas (Fig. 4). Errors in diagnosis were made in more than half of the observations. The results show that historical data can be helpful in lesion classification. The accuracy improved for the less experienced reviewers when history was available. The more experienced

BERQUIST

1254

ET AL.

AJR:155,

December

1990

Fig. 1.-Benign neuroma. A, Axial Ti-weighted MR image (SE 500/20) shows a well-marginated homogeneous lowintensity mass. B, Axial T2-weighted MR image (SE 2000/60)

shows uniform high signal intensity. Margination

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and signal intensity are typical of a benign lesion. Change in signal intensity between the two images indicates lesion is not a lipoma.

Fig. 2.-Fibrosarcoma of forearm. A, Axial Ti-weighted MR image (SE 500/20) shows mass with mixed or inhomogeneous signal intensity. B, Axial

T2-weighted

MR image

(SE

2000/60)

shows mass has irregular margins and inhomogeneous signal intensity. These features are typical of a malignant mass and appreciated more easily on T2-weighted image.

A, Axial Ti-weighted MR image (SE 500/20) shows scattered areas of increased signal intensity due to blood. B, Axial T2-weighted MR image shows areas of high and low intensity (arrowheads) due to paramagnetic effects of blood. Inhomogeneous signal intensity and irregular margins may cause

Fig. 4.-Synovial sarcoma in gluteal region. Coronal SE 500/20 MR image of pelvis shows wellmarginated cystic lesion with appearance similar to that of hematoma. Three of six synovial sarcomas were considered benign because of this ap-

this lesion

pearance.

Fig. 3.-Cavernous

hemangioma

to be confused

in proximal

with a malignant

forearm.

mass.

AJA:155,

December

MR

1990

OF

SOFT-TISSUE

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MR imaging reviewer relied on history minimally, and overall specificity of 96% for all lesions did not change tween the first and second portions of the study.

the be-

REFERENCES 1 . Beltran J, Simon DC, Katz W, Weis LD. Increased MR signal intensity in skeletal muscle adjacent to malignant tumors: pathologic correlation and clinical

relevance.

Radiology

1987;1 62:251-255

2. Bland KI, McCoy DM, Kinard RE, Copeland EM III. Application of magnetic resonance imaging and computerized tomography as an adjunct to the surgical management of soft tissue sarcomas. Ann Surg 1987;205: 473-481

3. Berquist TH. Magnetic resonance imaging of musculoskeletal

neoplasms.

Clin Orthop i989;244:101-118

4. Sundaram M, McGuire MH, Herbold DR, Beshany SE, Fletcher JW. High signal intensity soft tissue masses on Ti weighted pulsing sequences. Skeletal Radio! 1987;16:30-36 5. Sundaram M, McGuire MH, Herbold DR. Magnetic resonance imaging of soft tissue masses: an evaluation of fifty-three histologically proven tumors. Magn Reson Imaging i988;6:237-248 6. Berquist TH, Ehman AL, Richardson ML. Magnetic resonance of the musculoskeletal system. New York: Raven, 1987:85-108 7. Dooms GC, Hricak H, Sollitto RA, Higgins CB. Lipomatous tumors and tumors with fatty component: MR imaging potential and comparison of

MASSES

1255

MA and T results. Radiology 1985;157:479-483 8. Weekes AG, Berquist TH, McLeod AA, Zimmer WD. Magnetic resonance imaging of soft-tissue Magn Reson Imaging

tumors:

comparison

with

computed

tomography.

1985;3:345-352 9. Weekes AG, McLeod RA, Reiman HM, Pritchard DJ. CT of soft-tissue neoplasms. AJR 1985;144:355-360 10. Petasnick JP, Turner DA, charters JR. Gitelis 5, Zachanas CE. Soft-tissue masses of the locomotor system: comparison of MR imaging and CT. Radiology

1986;160: 125-133 M, McGuire MH, Schajowicz F. Soft-tissue masses: histologic basis for decreased signal (short T2) on T2-weighted MR images. AiR 1987;148: 1247-1 250 12. Totty WG, Murphy WA, Lee JKT. Soft-tissue tumors: MA imaging. Radio!ogy 1986;160:135-141

1 1 . Sundaram

13. Cohen EK, Kressel HY, Perosio T, et al. MR imaging of soft-tissue hemangiomas: correlation with pathologic findings. AJR 1988;150: 10791081 14. Cohen JM, Weinreb JC, Redman H. Arteriovenous malformations of the extremities:

MR imaging.

Radiology

1986;158:475-479

15. Cohen MD, McGuire W, Cory DA, Smith JA. MR appearance 16.

of blood and blood products: an in vitro study. AiR 1986;146: 1293-1 297 Ehman AL, Berquist TH. Magnetic resonance imaging of musculoskeletal trauma. Radio! Clin North Am 1986;24(2):291-319

17. Swensen SJ, Keller PL, Berquist TH, McLeod RA, Stephens DH. Magnetic resonance

imaging

of hemorrhage.

AiR

1985;145:921-927

18. Kransdorf MJ, Jelinek JS, Moser AP Jr, et al. Soft-tissue using MR imaging. AJR 1989;153:541-547

masses: diagnosis

Value of MR imaging in differentiating benign from malignant soft-tissue masses: study of 95 lesions.

MR imaging has largely replaced CT as the technique of choice for preoperative staging of patients with soft-tissue masses. Whether MR imaging can be ...
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