4. Benign Criteria of Bone Tumors
Well defined margin
Sclerotic rim
Expanding lesion
No periosteal reaction
No extraosseous soft tissue component
Narrow zone of transition
5. Malignant Criteria of Bone Tumors
Ill defined margins
Cortical destruction
Periosteal reaction
Extraosseous extension
Intra-articular invasion
Neurovascular bundle affection
Wide zone of transition
14. Bone Island (Enostosis)
a) Incidence Common
b) Location Predilection for pelvis , long bones , spine
and ribs
c) Associations Osteopoikilosis : multiple bone islands
d) Radiographic Features
Small round or oval foci of dense bone within the medullary space-
The appearance of radiating spicules at the margins that blend with the
surrounding trabeculae is pathognomonic
26. PERIOSTEAL
CHONDROMA
Slowly growing
Benign cartilaginous tumor of limited size
develops within and beneath the
periosteum on the surface of cortical bone.
Metaphyseal lesion in a tubular bone that
appears as an area of cortical indentation,
resulting in a scalloped, or saucerized
depression of the outercortex, with a well-
defined inner margin.
48. Periosteal Desmoid
AKA avulsive cortical irregularity / distal metaphyseal femoral
defect / cortical desmoid, or medial supracondylar defect of
the femur
Tumor-like fibrous proliferation of the periosteum predilection
for the posteromedial cortex of the medial femoral
condyle.associated with erosion of the underlying bone.
Periosteal desmoid usually occurs between the ages of 12
and 20 years, mainly in boys, and most lesions disappear
spontaneously by the end of the second decade. It
Represents an asymptomatic normal variant that does not
require biopsy or treatment.
56. Osteofibrous Dysplasia
(Kempson-Campanacci Lesion)
(formerly called ossifying fibroma) is a
rare disorder witha decided preference for
the tibia.
Characterized by the presence of fibrous
connective tissue and trabeculae of
immature nonlamellar bone rimmed by
osteoblasts
68. Intraosseous, cortical, or parosteal
nonaggressive lesions.
Radiolucent lesion with sharply defined
borders, associated with thinning and
bulging of the cortex particularlyin thin
bones such as the fibula or rib.
The central calcifications and ossifications
- a sign of fat necrosis that is seen in an
infarct of the fatty marrow.
Intraosseous Lipoma
72. Lipoma Arborescens
Villous lipomatous proliferation of the synovial
membranes
Nonneoplastic lipomatous proliferation of the
synovium
Soft tissue density within the joint, commonly
interpreted as “joint effusion.”
CT - Very little or non enhancing synovial
mass
MRI - Villous proliferation.
73. References
1.Yochum and Rowe’s ESSENTIALS OF SKELETAL RADIOLOGY
2.Adam Greenspan’s differential Diagnosis in Orthopaedic Oncology
Location Within Anatomic Regions :
a) Epiphysis :
1-Chondroblastoma
2-Infection
3-Geode
4-GCT
b) Metaphyseal :
-Lesions of different causes : neoplastic ,
inflammatory and metabolicc) Epiphyseal / Metaphyseal :
-GCT
d) Diaphysis :
-After the 4th decade of life , most solitary
diaphyseal bone lesions involve the bone
marrow
stippled calcification
The superior and inferioredges may be overhanging.
Multiple osteocartilaginous exostoses: magnetic resonance imaging (MRI). Coronal (A) and axial (B) T1-
weighted (SE, TR 600, TE 20) MR images show several sessile osteochondromas affecting the proximal femora. Observe
abnormal tubulation of the bones. C: In another patient with multiple cartilaginous exostoses MRI was performed because
one of the osteochondromas continued to enlarge. Sagittal T1-weighted (SE, TR 400, TE 12) image demonstrates intact
cortex covering the lesion. D: Axial fast-spin echo (FSE, TR 4000, TE 102 Ef) MRI shows high-intensity thin cartilaginous cap of
osteochondroma without malignant changes. E: Lack of malignant transformation was confirmed on axial inversion recovery
(FMPIR/90; TR 4000, TE 51 Ef, TI 140) MRI, which shows no soft tissue extension of the lesion (arrows).
Chondroblastoma: magnetic resonance
imaging (MRI). A: Conventional radiograph
shows a lesion (arrowheads) with a narrow zone of
transition in the left humeral head of an 18-yearold
man. Note benign-appearing layer of periosteal
reaction along the lateral cortex (arrow). B: Coronal
T1-weighted (SE, TR 600, TE 20) MRI shows
significant amount of perilesional edema. C: Axial
T2-weighted (SE, TR 2000, TE 80) MRI shows the
lesion exhibiting a heterogeneous signal.
CHONDROMYXOID FIBROMA. Proximal
Tibia. Note the eccentric, metaphyseal, geographic lesion
in the proximal third of the tibia. Endosteal scalloping
(arrows), along with bone expansion, is noted (arrowhead).
COMMENT: The most common location for chondromyxoid
fibroma is the proximal third of the tibia, as seen
in this case. About 50% of chondromyxoid fibromas
occur in the tibia, with other common sites being the
femur, humerus, fibula, ribs, and small bones of the hands
and feet.
possibilities
include nonossifying fibroma and fibrous dysplasia.
Nonossifying fibroma, unlike chondromyxoid fibroma,
rarely displays cortical ballooning or cortical destruction,
and a periosteal reaction is present only in lesions
that have sustained a pathologic fracture. Fibrous dysplasia,
in contrast to chondromyxoid fibroma, is centrally
located rather than eccentric, rarely shows internal
septations, and does not elicit a periosteal reaction
Chondromyxoid fibroma: magnetic resonance
imaging (MRI). A: Sagittal T1-weighted (SE, TR 600,
TE 19) MRI in a 10-year-old girl shows a well-demarcated
lesion in the plantar aspect of the calcaneus, displaying
low signal intensity. B: Two axial T1-weighted (SE, TR
600, TE 17) images show significant amount of peritumoral
edema. C: Sagittal T2-weighted (SE, TR 2000, TE
80) MRI shows the lesion displaying high signal intensity.
A sclerotic border is imaged as a rim of low signal
intensity.
SYNOVIOCHONDROMETAPLASIA: HIP. A. AP
Hip. Note the multiple punctate opacities throughout the
hip joint (arrows). No extrinsic bone erosions are present.
B. Bone Window Axial CT: Hip. Observe the calcified loose
bodies around the hip (arrows). Also carefully observe, by
comparing with the contralateral normal side, the increased
fat separating muscle planes (arrowhead) and the diminished
muscle mass of the gluteus maximus (G) owing to disuse
atrophy from long-standing hip dysfunction.
Nonossifying fibroma (NOF): magnetic resonance imaging (MRI). A: Anteroposterior radiograph shows a
radiolucent lesion with sclerotic border abutting the posteromedial cortex of the right femur. B: Sagittal T1-weighted MRI
shows predominantly low signal intensity of the lesion. C: Sagittal T2-weighted image shows heterogeneous but mostly high
signal intensity of NOF. D: Sagittal T1-weighted fat-suppressed MRI after intravenous injection of gadolinium shows slight
heterogeneous enhancement of the lesion.
Healed nonossifying fibroma. A lesion that
healed spontaneously may persist as a sclerotic patch. In this
sclerosing phase, nonossifying fibroma should not be mistaken
for osteoblastic tumor or bone island.
Nonossifying fibroma resembling an aneurysmal
bone cyst. A large lesion in the fibula exhibits an expansive
character and thus resembles an aneurysmal bone cyst.
Note, however, the absence of a periosteal reaction that is
invariably present in the latter lesion.
FIBROUS CORTICAL DEFECT: DISTAL FEMUR.
A. AP Knee. B. Lateral Knee. Note the eccentric, radiolucent
lesion within the distal medial metaphysis of the femur.
Observe the sclerotic margin and sharp zone of transition
around this lesion, suggesting a benign response. This
fibrous cortical defect was asymptomatic and found coincidentally
on radiographic examination to rule out a
fracture.
Benign fibrous histiocytoma. A: A 37-year-old
man presented with occasional pain in the right knee. An
oblique radiograph of the knee shows a lobulated radiolucent
lesion with a well-defined sclerotic border, located
eccentrically in the proximal tibia. B: A 16-year-old boy
presented with a painful tibial lesion that on radiography
looked like a nonossifying fibroma. Because of persistent
symptoms the lesion was biopsied and proved to be consistent
with a benign fibrous histiocytoma.
From the radiologic standpoint, the main differential
possibilities include NOF and giant cell tumor, particularly
when benign fibrous histiocytoma is situated at the articular
end of bone. The radiographic features of NOF may
be indistinguishable from those of benign fibrous histiocytoma,
although the more aggressive appearance of the
latter (such as an expanding border) and the location,
which is atypical for NOF, are the clues to the diagnosis.
Giant cell tumor only rarely exhibits a rim of reactive sclerosis,
whereas this is a common feature of benign fibrous
histiocytoma
Anteroposterior radiograph of the distal leg of a 17-year-old girl shows a
monostotic focus of fibrous dysplasia in the diaphysis of the tibia. Observe the slight expansion and thinning of the cortex and
the partial loss of trabecular pattern in the cancellous bone, which gives the lesion a “ground-glass” or “smoky” appearance.
B: Anteroposterior radiograph of the right hip in a 25-year-old man shows the focus of fibrous dysplasia in the femoral neck
that exhibits a more sclerotic appearance than that seen in A.
FIBROUS DYSPLASIA: POSITIVE BONE SCAN.
Note that this adult with polyostotic fibrous dysplasia shows
intense uptake in multiple lesions throughout the entire
skeleton. Active lesions in polyostotic fibrous dysplasia will
show intense uptake on nuclear medicine scans.
FIBROUS DYSPLASIA. A. PA Skull. Observe
the sclerotic and lytic lesions of fibrous dysplasia affecting
half of the skull table and facial bones. These changes have
distorted the orbit, creating a dense appearance to its floor
(arrows). B. Lateral Skull. Observe the well-delineated lesions
of fibrous dysplasia throughout the frontal and parietal
bones. Extensive facial bone involvement has produced
bony expansion, with a well-defined cortical margin (arrows).
C. Coronal CT Scan. Note the dense ground glass appearance
to the matrix of the lesion extending along the petrous
ridge of the temporal bone (arrow) into the ethmoid sinuses.
Polyostotic fibrous dysplasia: magnetic resonance imaging (MRI). A: Anteroposterior radiograph of the proximal
right leg of a 23-year-old woman shows a long lesion in the proximal tibia exhibiting a “ground-glass” appearance. The bone is mildly expanded and the cortex is thin. B: Coronal T1-weighted MRI shows the lesion to be multifocal with isointense signal similar to that of the skeletal muscles. C: Coronal T2-weighted MRI shows heterogeneous signal of the lesion ranging
from intermediate to high intensity. D: Coronal T1-weighted fat-suppressed MRI after intravenous injection of gadolinium demonstrates slight enhancement of the lesion
Figure 11-199 HEMANGIOMA: SUNBURST OR SPOKEDWHEEL
APPEARANCE. A. PA Skull. B. Lateral Skull. Note the
circular radiolucent defect present primarily within the temporal
bone, with minimal extension into the frontal bone.
There is an intense, radiating spiculation of bone from the
central portion of the lytic defect, creating the sunburst or
spoked-wheel appearance of an intraosseous hemangioma.
C. Tangential Skull. Observe the fine spicula radiating from
the centrum of the lytic hemangioma. D. CT Skull. Observe
the large, radiating hemangioma present within the table of
the skull. COMMENT: Hemangiomas affecting the calvaria
often present with dense, fine spicula radiating from the
centrum, creating a sunburst or spoked-wheel appearance.
The intense nature of the radiating spicules of bone can
mimic osteosarcoma, particularly in tangential or profile
views.
RADIOLUCENT slightly sclerotic border in the calcaneus
Sagittal T1-weighted (SE, TR 850, TE 15) MRI demonstrates homogeneous intermediate signal
intensity within the lesion, rimmed by low-signal-intensity sclerotic margin. C: Sagittal STIR MR image shows that the lesion
now is of homogeneous high signal intensity.
expansive radiolucent lesion in the metaphysis of the distal tibia, extending into the diaphysis. Note its eccentric
location in the bone and the buttress of periosteal reaction at the proximal aspect of the lesion
MRI scan of the lumbar spine sagittal T1 (a) and T2 (b) Weighted images and axial sections; (c and d) of T2 weighted images showing characteristic findings of aneurysmal bone cyst with multiple fluid-fluid levels
COCKADE SIGN
Lateral
radiograph of the knee of a 22-year-old woman
with several episodes of knee pain and swelling
shows fullness in the suprapatellar bursa that was
interpreted as joint effusion. Note also the increased
density in the region of the popliteal
fossa and subtle erosion of the posterior aspect of
the distal femur. B: Sagittal T1-weighted (SE, TR
800, TE 20) MRI shows a lobulated mass in the
suprapatellar bursa, extending into the knee joint
and invading the infrapatellar fat. Note also the
lobulated mass in the posterior aspect of the joint
capsule, extending toward the posterior tibia.
These masses exhibit an intermediate to low signal
intensity. The erosion at the posterior aspect
of the distal femur (supracondylar) is clearly
demonstrated by an area of low signal intensity
(arrow). C: Coronal T2-weighted (SE, TR 1800, TE
80) MRI demonstrates areas of high signal intensity
that represent fluid and congested synovium,
interspersed with areas of low signal intensity,
characteristic of hemosiderin deposits.
Femur: Osteochondromas in the pelvis. Sessile osteochondromas of the proximal right femoral neck
with both Sessile and pedunculated osteochondroma of the distal femur. Tibia and fibula: Pedunculated osteochondroma of the proximal fibula with more sessile osteochondroma of the proximal tibial diaphysis.
Solitary osteochondroma
Multiple enchondromatosis
Chondromsarcoma
Eccentric lucent lesions with sclerotic rims are located in the metaphyses of the femur and tibia. There is no pathologic fracture.
Nonossifying fibromas
Fibrous cortical defects
Aneurysmal bone cyst
Multiple heterogeneously enhancing (predominantly peripheral but with some band-like central enhancement), cortically based bilateral T1- and T2-hypointense lesions are seen in the distal femur and proximal tibial metaphyses, occupying 75% to 90% of the distal femoral metaphysis without pathologic fracture. These are healing nonossifying fibromas given the low signal intensity.
ortically based lesions in the metaphyses of long bones that initially are T2-hyperintense with a hypointense rim, but as they heal, they become hypointense on all sequences.
neurofibromatosis 1, fibrous dysplasia, and Jaffe-Campanacci syndrome.
Radiograph shows a well-circumscribed lucent lesion in the medial femoral condyle with a narrow zone of transition, measuring up to 3.2 cm and confined to the epiphysis without periosteal reaction.
Chondroblastoma
Chondrosarcoma (clear cell)
Intraosseous ganglion
Osteomyelitis (Brodie's abscess)
a contrast-enhanced MRI scan of the knee was performed. Click images to enlarge. In order: coronal T1-weighted, coronal short tau inversion-recovery (STIR), and sagittal fat-suppressed T2-weighted images
A T1-isointense, T2-mixed, is centered in the lateral aspect of the medial femoral condyle. It has a hypointense border, in keeping with surrounding sclerosis, with surrounding edema, extending into the soft tissues, including Hoffa's fat pad.
Top row: axial T1-weighted and STIR images. Bottom row: axial fat-suppressed T1-weighted precontrast and fat-suppressed T1-weighted postcontrast images. Right image: coronal fat-suppressed T1-weighted postcontrast image.
heterogeneously enhancing geographic epiphyseal lesion