DOI:10.2214/AJR.07.2796
AJR 2008; 190:1611-1615
© American Roentgen Ray Society
Incidental Enchondromas of the Knee
Michael J. Walden1,
Mark D. Murphey1,2,3 and
Jorge A. Vidal1,2
1 Department of Radiology, Walter Reed Army Medical Center, Washington, DC
20306.
2 Department of Radiologic Pathology, Armed Forces Institute of Pathology, 6825
16th St. NW, Bldg. 54, Washington, DC 20306.
3 Department of Radiology, Uniformed Services University of the Health Sciences,
Bethesda, MD.
Received June 29, 2007;
accepted after revision December 19, 2007.
Address correspondence to M. D. Murphey
(murphey{at}afip.osd.mil).
CME This article is available for CME credit. See
www.arrs.org
for more information.
The opinions or assertions contained herein are the private views of the
authors and are not to be construed as official or as reflecting the views of
the Department of the Army, the Department of the Navy, or the Department of
Defense.
FOR YOUR INFORMATION
This article is available for CME credit. See
www.arrs.org
for more information.
Abstract
OBJECTIVE. The purpose of our study was to determine the prevalence
of incidental enchondromas on routine MR knee imaging.
MATERIALS AND METHODS. We retrospectively reviewed 449 consecutive
routine knee MR examinations for the presence of enchondromas. MRI was
considered positive when a focal geographic area of lobular marrow replacement
(nonsubchondral) was identified on T1 weighting and high signal intensity was
seen on T2 weighting. Patients with enchondromas were further evaluated for
demographics; lesion site, size, and relationship to the physeal plate;
aggressive imaging features described with chondrosarcoma; concurrent internal
derangement; and study indication.
RESULTS. The prevalence of incidental enchondromas was 2.9% on
routine knee MR examinations. The prevalence was highest in the distal femur
(2.0%), followed by the proximal tibia (0.7%) and the proximal fibula (0.2%).
The average lesion size was 1.9 x 1.2 x 1.3 cm (57% of lesions
were < 1 cm). Most lesions were located in the metaphysis (71%) or
diaphysis (21%). Enchondromas were within 1.5 cm of the physeal plate in 72%
of cases. No aggressive imaging features to suggest chondrosarcoma were seen.
All patients had evidence of internal derangement as the cause of symptoms and
the request for imaging.
CONCLUSION. Incidental enchondromas can be identified on 2.9% of
routine MR knee examinations, most frequently in the distal femur (2.0%). This
significant prevalence is much higher than in an autopsy series (0.2%), likely
reflecting the increased sensitivity of MRI for detecting small lesions, and
is important to recognize to avoid confusion with other pathologic
entities.
Keywords: appendicular musculoskeletal system biomedical statistics enchondromas MRI radiologic-pathologic correlation
Introduction
Enchondroma is a benign neoplasm of the medullary canal com posed of
mature hyaline cartilage. Enchondroma is one of the most common osseous
neoplasms, representing 12-24% of all benign bone tumors and 3-10% of all bone
tumors [1,
2]. Of benign chondroid
lesions, it is second only to osteochondroma in frequency
[1,
2]. Intramedullary
chondrosarcoma is also relatively common, accounting for 20-27% of all primary
bone sarcomas and 8-17% of all bone tumors
[3-6].
Enchondroma and intramedullary chondrosarcoma can be difficult to distinguish
on imaging, although certain features, including the lesion size, degree of
endosteal scalloping, a rim of surrounding edema, and pain referable to the
lesion, favor the diagnosis of intramedullary chondrosarcoma
[7-13].
In our anecdotal experience, incidental enchondromas are commonly seen on
routine MRI of the knee. Because of the relatively high frequency of
enchondromas and their similarity to intramedullary chondrosarcomas, we
believe it is important to establish the prevalence of incidental enchondroma.
Although multiple studies have described the prevalence of these lesions among
bone tumors [1,
2,
14-16],
to our knowledge the literature describing the overall incidental prevalence
of these lesions (0.2%) is limited to a single autopsy series
[17]. It is therefore our
purpose to establish the frequency of enchondroma about the knee on routine MR
examinations.
Materials and Methods
Two radiologists retrospectively reviewed 463 consecutive routine knee MR
examinations from October 2004 to February 2005 for identification of
enchondromas, with agreement by consensus. Fourteen of the examinations were
eliminated as a result of extensive metallic artifact, leaving a total study
group of 449 MR examinations (434 patients, in 15 of whom bilateral MR knee
exami nations were evaluated). This study was approved by the Department of
Clinical Investigations of the Walter Reed Army Medical Center in compliance
with HIPAA. Informed consent was not required.

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Fig. 1A —Incidental enchondroma in distal femur of 51-year-old woman
with medial meniscal tear as cause of clinical symptoms. Sagittal T1-weighted
(A, TR/TE, 367/20) and fat-suppressed proton density-weighted
(B, 2,250/13) MR images show focal area of marrow replacement with high
signal intensity on long-TR image (arrows) in distal femoral
metaphysis. Lesion is centrally located in medullary canal, has mildly
lobulated borders, and is juxtaposed to old epiphyseal plate
(arrowheads, A).
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Fig. 1B —Incidental enchondroma in distal femur of 51-year-old woman
with medial meniscal tear as cause of clinical symptoms. Sagittal T1-weighted
(A, TR/TE, 367/20) and fat-suppressed proton density-weighted
(B, 2,250/13) MR images show focal area of marrow replacement with high
signal intensity on long-TR image (arrows) in distal femoral
metaphysis. Lesion is centrally located in medullary canal, has mildly
lobulated borders, and is juxtaposed to old epiphyseal plate
(arrowheads, A).
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Fig. 2A —Incidental enchondromas in distal femoral diaphysis of
24-year-old woman with anterior knee pain caused by patellofemoral disease.
Sagittal scout gradient-echo (TR/TE, 92/1.6; flip angle, 30°) MR image
shows two foci of marrow replacement in distal femoral diaphysis
(arrows).
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Fig. 2B —Incidental enchondromas in distal femoral diaphysis of
24-year-old woman with anterior knee pain caused by patellofemoral disease.
Axial fat-suppressed T2-weighted (4,650/36) MR image through more inferior
lesion reveals high signal intensity in eccentric intramedullary lesion and
mildly lobulated margins (arrowsheads). No endosteal scalloping is
present. Patient's symptoms and cause for MRI was patellofemoral disease (not
shown).
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MRI examinations were performed on four different imaging units that
operated at high field strength (1.5 T). Images available for review were from
three institutions and included T1-weighted (TR range/TE range, 350-700/13-40)
spin-echo or fast spin-echo, T2-weighted (3,650-4,350/80-110) spin-echo or
fast spin-echo, gradient-recalled echo (400-650/10-15), and proton
density-weighted with fat-saturation (1,500-4,850/13-50) images in the axial,
coronal, and sagittal-oblique planes. The field of view of all images ranged
from 140 to 160 mm. Slice interval was 3.5 or 4 mm on all images.
MRI was considered positive for enchondroma on identification of a focal
geographic (masslike) area of marrow replacement on T1-weighted images and
corresponding high signal intensity (similar to fluid) on T2-weighted images
with lobular margins on either pulse sequence. Lesions with similar
characteristics that were subchondral in location or had associated overlying
hyaline cartilaginous defects were excluded as representing subchondral cysts,
intraosseous ganglia, or subchondral edema or contusion.
Patients with lesions that met these imaging criteria were further
evaluated for lesion site (femur, tibia, or fibula), patient demographics (sex
and age and compared with the total patient population), lesion size (in three
dimensions and distinction of lesions into two groups as those less than or
greater than 1 cm in maximal dimension), longitudinal and axial location in
the marrow (epiphyseal, metaphyseal, or diaphyseal; and central or eccentric),
relationship of the lesion to the physeal plate (abutting the physeal plate,
not adjacent to but within 1.5 cm of the physeal plate, or > 1.5 cm from
the physeal plate [and average lesion size for enchondromas within 1.5 cm of
the plate vs farther than 1.5 cm]), evidence of endo steal scalloping (greater
than or less than two thirds of the normal cortical thickness, if present),
presence of an associated soft-tissue component, presence or absence of
surrounding marrow edema, and concurrent findings of internal de rangement
(e.g., meniscal tears, cruciate ligament injuries, hyaline cartilage defects,
or colla teral ligament injuries). In studies positive for the presence of
enchondroma, the indication for ordering each examination was reviewed to
deter mine whether the primary suspicion was internal derangement of the knee
or whether a primary osseous lesion was suspected.
A search for other imaging techniques such as radiography, bone
scintigraphy, and CT was made in all cases in which an enchondroma was
identified on MRI for purposes of correlation. Only three patients had
correlative images, all of which were radiographs. These were evaluated for
the following features: the presence or absence of a mixed lytic and sclerotic
lesion, presence or absence of matrix mineralization showing a typical
chondroid "arc and ring" appearance as the cause of the lesion
sclerosis, lesion size, and endosteal scalloping less than or greater than two
thirds of the normal cortical thickness (if present).
Results
We found 14 (3.1%) enchondromas about the knee in 13 (2.9%) patients (one
patient had two enchondromas, both in the distal femoral diaphysis). Nine
cases were in the femur (2.0%) (Figs.
1A,
1B,
2A,
2B,
3A,
3B,
4A,
4B,
4C and
4D), three in the tibia (0.7%)
(Figs. 5A and
5B), and one in the fibula
(0.2%). Of the 13 patients with lesions, seven were male from 254 males in the
total patient population. Six female patients had lesions of 180 females in
the total sample population. Age varied from 10 to 83 years (average, 40.1
years) in the total sample population, whereas the age of patients with
lesions varied from 24 to 53 years (average, 36.4 years). Size range of
enchondromas varied from 0.3 x 0.3 x 0.4 cm to 4.0 x 2.2
x 2.6 cm (average, 1.9 x 1.2 x 1.3 cm). The maximal
dimension of the lesions was less than 1 cm in 57% (n = 8) and larger
than 1 cm in 43% (n = 6). The lesions were located in the metaphysis
in 71% (n = 10) (Figs.
1A,
1B,
4A,
4B,
4C,
4D,
5A and
5B) of cases, in the epiphysis
in 7% (n = 1), and in the diaphysis in 21% (n = 3) (Figs.
2A and
2B). The lesions were located
centrally in the medullary canal in 57% (n = 8) and eccentrically in
43% (n = 6). The lesions abutted the physeal plate in 43% (n
= 6) of cases (Figs. 1A,
1B,
4A,
4B,
4C,
4D,
5A and
5B) and were within 1.5 cm of
the physeal plate in 29% (n = 4) of lesions. The remaining 29% of
lesions (n = 4) were more than 1.5 cm from the physeal plate (Figs.
2A,
2B,
3A and
3B). The average lesion size of
enchondromas less than 1.5 cm from or abutting the physeal plate was 1.2
x 0.8 x 0.9 cm. The average lesion size of enchondromas more than
1.5 cm from the epiphyseal plate was 1.2 x 0.9 x 1.0 cm.

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Fig. 3A —Minute enchondroma or cartilage rest in distal femur of
33-year-old man with knee pain associated with quadriceps and patellar tendon
tendinopathy. Coronal T1-weighted (A, TR/TE, 400/18) and fat-suppressed
T2-weighted (B, 4,417/41) MR images show minute focal area of marrow
replacement with prominent high signal intensity on long-TR image in distal
femoral metadiaphysis (arrows). Lesion reveals minimally lobulated
margins on T2-weighted image and is more than 1.5 cm from physeal scar
(arrowheads). Cause for MRI was quadriceps and patellar tendon
tendinopathy (not shown).
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Fig. 3B —Minute enchondroma or cartilage rest in distal femur of
33-year-old man with knee pain associated with quadriceps and patellar tendon
tendinopathy. Coronal T1-weighted (A, TR/TE, 400/18) and fat-suppressed
T2-weighted (B, 4,417/41) MR images show minute focal area of marrow
replacement with prominent high signal intensity on long-TR image in distal
femoral metadiaphysis (arrows). Lesion reveals minimally lobulated
margins on T2-weighted image and is more than 1.5 cm from physeal scar
(arrowheads). Cause for MRI was quadriceps and patellar tendon
tendinopathy (not shown).
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Fig. 4A —Incidental enchondroma of distal femur and small subchondral
cyst or intraosseous ganglion in 53-year-old woman with knee pain associated
with medial and lateral meniscal tears. Coronal T1-weighted (A, TR/TE,
550/15) and fat-suppressed T2-weighted (B, 4,867/50) MR images reveal
proximal tibial epiphyseal lesion with marrow replacement and high signal
intensity on long-TR image (arrows). These intrinsic MR
characteristics simulate enchondroma.
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Fig. 4B —Incidental enchondroma of distal femur and small subchondral
cyst or intraosseous ganglion in 53-year-old woman with knee pain associated
with medial and lateral meniscal tears. Coronal T1-weighted (A, TR/TE,
550/15) and fat-suppressed T2-weighted (B, 4,867/50) MR images reveal
proximal tibial epiphyseal lesion with marrow replacement and high signal
intensity on long-TR image (arrows). These intrinsic MR
characteristics simulate enchondroma.
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Fig. 4C —Incidental enchondroma of distal femur and small subchondral
cyst or intraosseous ganglion in 53-year-old woman with knee pain associated
with medial and lateral meniscal tears. Sagittal T1-weighted (C,
550/15) and gradient-echo (D, 577/10; flip angle, 30°) MR images
reveal cleftlike extension to subchondral bone (arrowheads) that
shows high signal intensity on long-TR and gradient-echo images. This feature
is not seen in enchondromas and suggests correct diagnosis of subchondral cyst
or intraosseous ganglion. Note distal femoral enchondroma (arrows)
with typical features on sagittal images.
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Fig. 4D —Incidental enchondroma of distal femur and small subchondral
cyst or intraosseous ganglion in 53-year-old woman with knee pain associated
with medial and lateral meniscal tears. Sagittal T1-weighted (C,
550/15) and gradient-echo (D, 577/10; flip angle, 30°) MR images
reveal cleftlike extension to subchondral bone (arrowheads) that
shows high signal intensity on long-TR and gradient-echo images. This feature
is not seen in enchondromas and suggests correct diagnosis of subchondral cyst
or intraosseous ganglion. Note distal femoral enchondroma (arrows)
with typical features on sagittal images.
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Fig. 5A —Incidental enchondroma in proximal tibia of 32-year-old woman
with meniscal tear. Coronal T1-weighted (A, TR/TE, 500/15) and sagittal
fat-suppressed T2-weighted (B, 4,000/103) MR images show small focal
area of marrow replacement (arrows). Lesion reveals high signal on T2
weighting, has mildly lobular borders, is juxtaposed to epiphyseal plate scar
(arrowheads, A), and is slightly eccentrically located in
medullary canal.
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Fig. 5B —Incidental enchondroma in proximal tibia of 32-year-old woman
with meniscal tear. Coronal T1-weighted (A, TR/TE, 500/15) and sagittal
fat-suppressed T2-weighted (B, 4,000/103) MR images show small focal
area of marrow replacement (arrows). Lesion reveals high signal on T2
weighting, has mildly lobular borders, is juxtaposed to epiphyseal plate scar
(arrowheads, A), and is slightly eccentrically located in
medullary canal.
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None of the lesions had evidence of endosteal scalloping, a soft-tissue
component, or surrounding marrow edema. All patients with enchondromas had
accompanying abnormalities of internal derangement identified on MRI that
corresponded to the patient's complaints and were the cause of the imaging
being performed.
Radiographs were available for correlation in three cases. In one patient,
a mixed lytic and sclerotic lesion with typical "arc and ring"
chondroid matrix mineralization (causing the lesion sclerosis) was seen and
measured 4.0 x 2.2 x 2.6 cm. In the other two patients, the
radiographs were normal and no lesion could be identified corresponding to the
MR abnormality. No evidence of endosteal scalloping was seen in any of these
three lesions at radiography.
Discussion
Our study confirms the significant prevalence of enchondroma affecting the
osseous structures about the knee. These lesions were identified on 2.9% of
routine MR knee examinations. The significant frequency of these lesions about
the knee should be recognized in order to avoid confusion with or
misinterpretation of other pathologic entities.
The most frequently encountered site of incidental enchondroma was the
distal femur (2.0%, n = 9), followed by the proximal tibia (0.7%,
n = 3), and the proximal fibula (0.2%, n = 1). The distal
femoral prevalence of 2.0% is 10 times higher than that in an autopsy series
that showed only two enchondromas in 1,125 right distal femurs specimens
(0.2%) of patients older than 25 years
[17]. In this autopsy series,
the overall prevalence of incidental enchondromas in the femur was 1.8%, with
most lesions described as proximal between the femoral head and neck
[17]. The reason for the
higher prevalence of enchondromas on imaging as compared with the autopsy
series is likely related to the increased sensitivity of MRI in identifying
small lesions that would not be apparent at typical gross pathologic
sectioning thickness and intervals
[17]. Only those lesions
visible to the naked eye on the gross pathologic sections underwent further
histologic analysis in the autopsy series
[17]. This concept is
supported by the small size of many of our lesions; 57% of the lesions were
smaller than 1 cm in maximal dimension.
We believed that most of the lesions would be closely related to the
physeal plate. This was based on the theory, with which we agree, that
enchondromas originate as cartilage rests derived from the physeal plate
[8,
17]. Indeed, 71% (n =
10) of enchondromas were within 1.5 cm of the physeal plate and 43%
(n = 6) abutted the physeal plate. Only 29% of enchondromas were more
than 1.5 cm from the physeal plate. In addition, we believed that lesions of
increased distance from the physeal plate might be larger because they arose
earlier and had more time available for potential growth. However, we found no
significant difference in the average size of enchondromas less than 1.5 cm
from or abutting the physeal plate (1.2 x 0.8 x 0.9 cm) compared
with those more than 1.5 cm from the physeal plate (1.2 x 0.9 x
1.0 cm). This finding probably reflects the indolent natural history of these
lesions, most of which have a limited potential for growth.
None of the lesions in our study had imaging or clinical features that
could have been described as suggestive of intramedullary chondrosarcoma. The
average maximal diameter of enchondromas in our study was 1.9 cm, a figure
that agrees with previous studies, indicating that size is a significant
discriminator between enchondromas and intramedullary chondrosarcomas
[7,
8,
13]. In particular, lesions
greater than 4.0 cm were more likely to be intramedullary chondrosarcomas in
the study by Kendell et al.
[13]. The small size of the
lesions is also the probable reason that only one of the three enchondromas
was visible on radiographic evaluation. In our series, 57% (n = 8) of
lesions were smaller than 1 cm in maximal dimension; in dictating our reports,
we refer to lesions of this size as "cartilaginous rests." In our
opinion, this terminology emphasizes the indolent nature of these lesions.
There is also limited or no value in recommending correlation with radiographs
in these lesions. We reserve the designation of enchondroma for lesions larger
than 1 cm in maximum dimension, which constituted 43% (n = 6) of the
lesions in our study.
No lesions were seen to have peritumoral marrow edema, another imaging
finding that suggested chondrosarcoma in the series by Janzen et al.
[12]. Deep endosteal
scalloping greater than two thirds of the normal cortical thickness has also
been described as an imaging feature that allows distinction of enchondroma
from intramedullary chondrosarcoma in long bone lesions
[7,
8]. Only one of the lesions in
our study was adjacent to the endosteum, and no significant endosteal
scalloping was seen in this patient. Pain referable to the lesion is a
clinical feature that is helpful to suggest the diagnosis of intramedullary
chondrosarcoma as opposed to enchondroma of long bones, which is frequently
asymptomatic [7,
8,
11]. All patients with lesions
in our series had concurrent abnormal findings on MRI that corresponded to the
indication for imaging. We therefore presumed that each lesion was
asymptomatic and incidentally detected
[7,
8,
11]. None of the patients with
enchondromas was imaged for evaluation of an osseous lesion.
Some limitations of this study include its retrospective nature and the
lack of uniformity in imaging parameters because of the multiplicity of
imaging centers. In addition, the diagnosis of the presumed enchondroma was
not confirmed pathologically, although such confirmation is naturally limited
to the realm of autopsy series. However, we were stringent in our criteria for
designating a lesion an enchondroma (Figs.
5A and
5B). Only medullary lesions
with lobular borders, geographic (masslike) marrow replacement, and typical
intrinsic characteristics were included (Figs.
5A and
5B). Lesions in a subchondral
location or with overlying hyaline cartilaginous defects were excluded. We
believe this eliminated inclusion of any intraosseous contusions, subchondral
cysts, intraosseous ganglia, or subchondral edema that could show similar
intrinsic characteristics. Despite these limitations, we believe our results
accurately represent the prevalence of these lesions.
In conclusion, we found that incidental enchondromas can be identified in
2.9% of routine MR knee examinations. They are most frequently encountered in
the distal femur (2.0%), followed by the proximal tibia (0.7%) and the
proximal fibula (0.2%). The prevalence in the distal femur is much higher than
that seen in an autopsy series (0.2%), which is likely related to the
increased sensitivity of MRI in identifying small lesions. These lesions show
no aggressive features that have been associated with intramedullary
chondrosarcoma. In our opinion these lesions do not require imaging follow-up,
although radiographs of larger enchondromas may serve as a useful inexpensive
baseline examination unless new symptoms related to the lesion become
clinically apparent. The significant frequency of these lesions about the knee
is important to recognize in order to avoid confusion with other pathologic
entities.
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