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MRI Web Clinic - October 2009

Developmental Variants

Clinical history: An 8 year old gymnast who injured the knee 5 days ago presents with posterior knee pain. (1a) T1 and (1b) fat suppressed proton density-weighted sagittal images are provided.

What is the finding? What is your diagnosis?

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1b

Figure 1:

(1a) T1 and (1b) fat suppressed proton density-weighted sagittal images

Findings

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2b

Figure 2:

A (2a) T1-weighted sagittal image of the knee shows a clearly demarcated region (arrow) with signal similar to fatty marrow in the posterior aspect of the femoral epiphysis.  The (2b) T2-weighted sagittal image shows subtle signal changes (arrow) of the subchondral bone marrow and intact articular cartilage (arrowheads).

 

Diagnosis

Normal developmental irregular ossification of the lateral femoral condyle.

Introduction

Irregular ossification of the distal femoral epiphysis is a common observation on radiographs in children and is frequently bilateral, but not always symmetrical 1. The normal variation in the ossification of the femoral condyle can mimic osteochondritis dissecans (OCD), and several MR imaging features are helpful in distinguishing this normal variant from OCD.

Discussion

The secondary center of ossification forms at an early stage of skeletal maturation. It is spherical and smooth in contour and is located in the central portion of the cartilaginous precursor. As the bony epiphysis continues to enlarge by means of enchondral ossification, the margins of the epiphysis may appear irregular or fragmented, simulating OCD or an acute fracture. Common locations for this imaging pitfall are the distal femoral epiphysis, the trochlea of the elbow and the tarsal navicular. In these regions, several small foci of ossification will eventually merge and appear solid.

Normal irregular ossification of the femoral condyles was present in 66% of the boys and 44 % of the girls 1 in a review of knee radiographs of 147 healthy, asymptomatic children between the ages of 3 and 13 years. The lateral condyle was involved in 44 % and the medial condyle in 12 %. The changes were frequently bilateral, but were not symmetrical. The regions of irregularity on radiographs have been found to decrease in size or disappear spontaneously within a mean observation period of 3.5 months 2. In a study utilizing knee MRI of 4 asymptomatic boys between the ages of 8 and 11 years with irregularity of the lateral femoral condyle it was shown that the radiolucent zones on the radiographs represented uncalcified cartilage 2. Location in the inferocentral posterior femoral condyles with intact overlying articular cartilage, accessory ossification centers, spiculations, residual cartilaginous model, and lack of bone marrow edema are features of normal variant ossification in this region 2,3.

Additional examples of normal irregular ossification are provided.

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Figure 3:

Irregularity of the medial femoral condyle (arrow) on a (3a) radiographic notch (tunnel) view simulating OCD.

 

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Figure 4:

11 year old boy with normal variant irregular ossification of the posterior aspect of the lateral femoral condyle (arrow) on a (4a) proton density sagittal image. The signal of the surrounding marrow is normal and the overlying articular cartilage is intact.

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Figure 5:

A coronal T1-weighted image shows normal irregular ossification of the lateral femoral condyle (arrow). Note the typical inferocentral location of the irregular ossification as opposed to OCD, which often involves the margin of the intercondylar notch.

 

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Figure 6:

Lateral radiograph in a 12 year-old boy with knee pain. Focal flattening and irregularity of the articular surface of the lateral femoral condyle (arrow) is evident.

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Figure 7:

A gradient-echo sagittal image of the same patient. The small accessory ossification nucleus (arrow) has an OCD-like appearance. The thin rim of uncalcified cartilage should not be mistaken for a subchondral fracture. The overlying articular cartilage is normal. No marrow edema was present on water sensitive sequences.

 

Differential diagnosis

Care should be taken not to misdiagnose the normal irregular ossification as stage I OCD, because the accepted treatment of stage I OCD is restriction of activity, which may have a negative effect on patient lifestyle.

75% of cases of OCD of the knee are located in the posterolateral aspect of the medial femoral condyle, often extending into the intercondylar region. The lateral condyle is involved in 20% of patients and both knees are affected in one third of patients. The peak incidence is around 12 to 13 years of age 4,5.

It has been postulated that the rather favorable prognosis of juvenile OCD in the knee could be partially explained by the erroneous diagnosis of developmental variants of ossification as stage-I OCD 3 (articular cartilage thickening with abnormal signal).

 

8a

Figure 8:

OCD of the lateral aspect of the medial femoral condyle (arrow). A fat-suppressed T2-weighted coronal image reveals surrounding marrow edema (arrowheads), mild focal thinning of the overlying articular cartilage (small arrow), and extension of the lesion into the intercondylar region.

 

In addition to normal irregular ossification of the femoral condyles, there are a number of additional variants related to skeletal maturation that have been recognized. Several of these variants will be demonstrated in the following cases.

Posterior metaphyseal stripe

In children and young adults there is subperiosteal fibrovascular tissue which is most prominent at the metaphyseal levels of the long bones. On MRI the normal subperiosteal tissue is best appreciated in the posterior aspect of the distal femur and appears as a thin stripe of bright signal on water-sensitive images. It enhances intensely after the administration of contrast material because of its rich vascularization. A similar metaphyseal stripe is frequently seen in the proximal tibial metaphysis. After skeletal maturity, the metaphyseal stripe disappears 6,7.

 

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Figure 9:

A fat-suppressed T2-weighted sagittal image shows a normal metaphyseal stripe (arrowheads) in the posterior femoral metaphysis.

 

Avulsive cortical irregularity

Also known as distal femoral cortical irregularity, distal femoral metaphyseal irregularity and cortical desmoid, this variant represents a fairly common incidental imaging finding along the posterior aspect of the medial distal femur, 1-2 cm proximal to the physis. Some investigators have implicated a traumatic cause, related to an avulsive injury, while others consider this entity developmental in origin. Cystic and proliferative variants have been described. The cystic type is considered a fibrous cortical defect and appears as a cortical lucency or excavation on radiographs lateral to the medial supracondylar ridge of the femur. The proliferative type occurs along the medial supracondylar ridge of the femur and has regions of speculation or irregularity. T1-weighted images show low signal intensity and T2-weighted images show variable signal intensity within the lesions. Occasionally, an MRI is ordered when the lesion mimics an aggressive neoplasm, such as an osteosarcoma, on radiographs 8,9,10.

 

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10b

Figure 10:

(10a) T1-weighted sagittal and (10b) fat-suppressed proton density-weighted axial images demonstrate a small avulsive cortical irregularity of the cystic type (arrows) within the posteromedial aspect of the distal femur.

 

Hematopoietic marrow

Residual red marrow is frequently present in the metaphyseal and adjacent diaphyseal portions of the femur and tibia in children, and may simulate abnormalities such as neoplastic infiltration, stress reaction and contusion. The regions of normal red marrow are longitudinally oriented with straight margins and have a base at or adjacent to the physis. On T1-weighted images they should always be of increased signal relative to muscle 7. On T2-weighted images the hematopoietic marrow is hyperintense due to its high water content with signal that approximates that of muscle. After the administration of contrast material, red marrow enhances to a higher degree than fatty marrow because it is more vascularized 11.

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11b

Figure 11:

(11a) T1 and (11b) fat suppressed proton density- weighted images showing normal red marrow (arrows) as hypointense on T1 and moderately hyperintense on proton density weighted images. The red marrow has a striated and flame-shaped appearance in the metaphyses and diaphyses of the femur and tibia in a 13 year-old male. As is typical, the red marrow spares the epiphyseal regions.

 

Bipartite patella

A bipartite patella is a result of failure of fusion of a secondary ossification center and should not be mistaken for an acute fracture. It is frequently bilateral in distribution and can be a cause of pain if there is disruption of its synchondrosis. A classification system according to Saupe 12 is based on location. Type I is at the inferior pole of the patella and is seen in 1% of cases. Type II is at the lateral margin of the patella and constitutes 20% of cases. Type III is in the superolateral patella and is the most common, found in 75% of cases. MR findings associated with a symptomatic bipartite patella include edema in the bipartite fragment (usually type III), abnormal signal across the synchondrosis, and cartilage discontinuity 13,14,15.

 

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Figure 12:

3D rendering depicting the 3 types of bipartite patella.

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Figure 13:

Incidental bipartite patella in two different patients on (13a,13b) fat-suppressed coronal T2-weighted images.

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Figure 14:

Symptomatic bipartite patella in a 14-year old male figure skater on a (14a) fat-suppressed T2-weighted sagittal image. Marrow edema (arrowheads) is present in and around the bipartite fragment as a result of chronic chondro-osseous tensile failure across its synchondrosis.

 

 

Dorsal defect of the patella

A dorsal defect of the patella is a variant related to normal ossification, present in 0.3 to 1 % of the population, located in the superolateral aspect of the articular surface of the patella. Histologically, it consists of fibrosis with or without bone necrosis. The cartilage over a dorsal defect is usually, but not always, intact. It may be a source of patellofemoral symptoms and knee pain. On T1-weighted images the signal of a dorsal defect is inhomogeneous and on gradient echo images the signal is equal to or greater than that of the cartilage. Healing may occur spontaneously 16.

 

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Figure 15:

Axial fat-suppressed proton density weighted image of the knee demonstrates a dorsal defect of the patella (arrow).

 

Normal variant accessory ossification center at the inferior pole of the patella

A focus of bone at the lower pole of the patella may represent a normal variant, a patellar sleeve fracture (acute osteocartilaginous avulsion of the lower pole of the patella), Sinding-Larsen-Johansson disease or patellar tendinopathy (jumper’s knee). The normal accessory center may be single or multiple and may or may not be separated from the patella. MR imaging is important for the correct diagnosis in the child with anterior knee pain 8.

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Figure 16:

Normal ossification center at the inferior pole of the patella (arrows) on a (16a) lateral radiograph and a (16b) T1- weighted sagittal image. Note also normal irregular ossification at the anterior surface of the patella (arrowhead), seen best on plain film. T2-weighted images in this patient revealed no edema to suggest a traumatic etiology.

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Figure 17:

A lateral radiograph shows a small focus of ossification (arrow) at the inferior pole of the patella in a 12 year-old male runner with chronic anterior knee pain.

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Figure 18:

Marrow edema (arrow) is evident within the inferior pole of the patella on a corresponding fat-suppressed T2-weighted sagittal image, consistent with Sinding-Larsen-Johansson disease.

 

Conclusion

In order to properly evaluate findings in pediatric knee MR imaging, it is essential to be aware of the variant changes of the osseous structures that occur with age. Imaging pitfalls in children are often related to normal variations in ossification patterns of the femoral condyles, tibia and patella. It is also important to keep in mind that some developmental variants may become symptomatic. MRI is an excellent modality in the pediatric setting because of its ability to provide accurate assessment of bone marrow and cartilage without the use of ionizing radiation.

Additional normal variants of the knee have been discussed by Dr Carroll in the December 2007 Radsource MRI Web Clinic.

References

1 Caffey J, Madell SH, Royer C, et al. Ossification of the distal femoral epiphysis. J Bone Joint Surg Am 1958; 40:647-54.

2 Nawata K, Teshima R, Morion Y, et al. Anomalies of ossification in the posterolateral femoral condyle: assessment by MRI. Pedatr Radiol 1999;29(10):781-4.

3 Gebarski K, Hernandez RJ. Stage I osteochondritis dissecans versus normal variant ossification in the knee in children. Pediatr Radiol 2005; 35(9): 880-6.

4 Bradley J, Dandy DJ. Osteochondritis dissecans and other lesions of the femoral condyles. J Bone Joint Surg Br 1989; 71:518-22.

5 Schenk RC Jr, Goodnight JM. Current concept review- osteochondritis dissecans. J Bone Joint Surg Am, 1996; 78: 439-56.

6 Laor T, Chun GF, Dardzinski BJ, Bean JA, Witte DP. Posterior distal femoral and proximal tibial metaphyseal stripes at MR imaging in children and young adults. Radiology 2002; 224:669-674.

7 Laor T, Jaramillo D. MR imaging Insights into skeletal maturation: What is normal? Radiology; 2009; 250: 28-38.

8 Mellado JM, Ramos A, Salvado E, et al. Avulsion fractures and chronic avulsion injuries of the knee: role of MR imaging. Eur Radiol 2002; 12(10):2463-73.

9 Stacy GS. Contour irregularities of the distal femur caused by developmental, traumatic, and benign cortically based neoplastic conditions: radiographic and MRI correlation. Clin Radiol 2004; 59 (9): 793-802.

10 Resnick D, Kang HS, Pretterklieber, ML. Internal Derangement of Joints, 2nd ed. 2007. Saunders.

11 Dwek JR, Shapiro F, Laor T, Barnewolt CE, Jaramillo D. Normal gadolinium-enhanced MR images of the developing appendicular skeleton. Am J Roentgenol, 1997;169:191-196.

12 Saupe H. Knochenmark Seilerung der Kniescheibe. Deutsch Z Chir 1943; 258:386

13 Ogden JA, McCarthy SM, Jokl P. The painful bipartite patella. J Pediatr Orthop 1982; 2:263.

14 Green WT Jr. Painful bipartite patellae: A report of three cases. Clin Orthop 1975; 110:197

15 Elias DA, White LM. Imaging of patellofemoral disorders. Clin Radiol 2004; 59(7): 543-57.

16 Ho VB, Kransdorf MJ, Jelinek JS, et al. Dorsal defect of the patella: MR features. J Comput Assist Tomogr 1991; 15:474.

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