|Year : 2015 | Volume
| Issue : 1 | Page : 36-38
Synovial chondromatosis in a young child: A rare presentation
Kuppa Srinivas, Dema Rajaiah, Yerukala Ramana, Puppula Kiran Kumar
Department of Orthopaedics, Kurnool Medical College, Kurnool, Andhra Pradesh, India
|Date of Web Publication||16-Mar-2015|
Dr. Kuppa Srinivas
Government General Hospital, Kurnool, Andhra Pradesh
Source of Support: None, Conflict of Interest: None
Synovial chondromatosis is a benign cartilaginous metaplasia of the synovium, which may affect any synovial joint. Knee joint is the most commonly involved joint presenting with pain swelling and restricted movements. It usually occurs aged 30 to 50 years and is extremely rare in children. Diagnosis is made by radiographs, computed tomography, magnetic resonance imaging and on surgery.
Keywords: Synovial chondromatosis, young child, knee joint
|How to cite this article:|
Srinivas K, Rajaiah D, Ramana Y, Kumar PK. Synovial chondromatosis in a young child: A rare presentation. J NTR Univ Health Sci 2015;4:36-8
|How to cite this URL:|
Srinivas K, Rajaiah D, Ramana Y, Kumar PK. Synovial chondromatosis in a young child: A rare presentation. J NTR Univ Health Sci [serial online] 2015 [cited 2019 Aug 20];4:36-8. Available from: http://www.jdrntruhs.org/text.asp?2015/4/1/36/153318
| Introduction|| |
Synovial chondromatosis is an unusual proliferative and metaplastic disorder, which is characterized by the formation of multiple cartilaginous nodules in the synovial membrane of the joint, tendon sheath and the bursae, the etiology of the disease is uncertain.  It is usually mono articular, knee joint is the most commonly affected.  It occurs twice as frequently in men than in women and usually presents with pain and swelling during the third to the fifth decade.  Multiple discreet nodules presenting as intra-articular loose bodies is the hallmark. The patient experiences a decreased range of motion, palpable swelling, effusion and crepitus.  Trauma, infections and fibroblast growth factors-9 (FGF-9) have been implicated in the pathogenesis. 
| Case Report|| |
A 10-year-old girl presented to the outpatient department with 4 months history of swelling the left knee with occasional pain. There was no history of trauma and no other joints were involved. Her past history family history and general health were un-remarkable.
Girl had normal gait was unable to squat due to discomfort in the knee. The left knee was moderately swollen with mild tenderness over the anterior aspect. The range of motion was from full extension to 90° of flexion. The knee was stable. One centimeter of wasting of the quadriceps was present. All other joints were normal.
The patient's blood tests were normal serum calcium, phosphate, erythrocyte sedimentation rate, C-reactive protein, white cell count. Rheumatoid arthritis factor and antinuclear antibody were not detected.
Plain radiograph revealed multiple calcific densities within the soft tissues around although some appeared to be in the joint, majority were in the suprapatellar pouch and popliteal fossa [Figure 1]. There was no ligamentous calcification and the growth plates were normal. To further scrutinize a magnetic resonance imaging (MRI) was taken and it showed extensive thickening of the synovium, multiple intra-articular calcific and ossific loose bodies and large calcified bursal extensions, consistent with synovial chondromatosis [Figure 2] and [Figure 3].
In a bloodless field, a lateral parapatellar incision was made when the synovial membrane was opened straw colored fluid extruded in large amounts containing many cartilaginous loose bodies, which were 2-4 mm in diameter. Many more were attached to the synovial membrane. A large pedunculated mass was present in the supra patellar pouch. This along with other pieces of synovium were excised and sent for histopathological examination [Figure 4]. The joint was washed to remove any leftover loose bodies after doing synovectomy. Wound was closed in layers patient recovered well and was discharged a week after surgery [Figure 5] and [Figure 6].
Gross pathology - Irregular surface multinodular specimen of size 11 cm × 7 cm × 3 cm. Partly covered with membrane c/s nodular and bony hard multiple gray white nodules of twenty in number [Figure 4].
Microscopy - Multiple sections studied shows synovial tissue with multiple benign looking cartilaginous nodules. Focal areas show trabeculae of mature bone. Macroscopic and histological examination of the specimen confirmed the diagnosis of synovial chondromatosis.
Patient followed regularly at 4-week interval. There is no clinical, radiological evidence of recurrence, and there is no limitation in knee movements. Patient is able to walk and squat without any difficulty.
| Discussion|| |
Synovial chondromatosis involves major joints such as knee, hip, shoulder, elbow and temporomandibular joint.  Other rare sites are distal radio ulnar joint, acromioclavicular joint facet joint, metacarpophalengeal joint and the spine. Presents as monoarticular pathology with pain and swelling along with the presence of intra capsular lesions. Lesions can invade the capsule and present as extra capsular masses. 
Occurs in two forms:
- Primary form which results from metaplasia of the synovium, which produces multiple loose bodies within the joint they progress to calcify loose bodies which are of the same size. Eventually, they embed in the synovium and they do not float freely in the joint.
- Secondary form is much more common believed to be secondary to trauma which causes shedding of bits of articular cartilage resulting in loose bodies in the joint. They may or may not calcify. Unlike primary these loose bodies are of different sizes and generally fewer in number. Generally, osteoarthritis is present due to articular cartilage damage.
Early-active intra synovial disease but no loose bodies. 
Transitional-active disease and loose bodies.
Late-multiple loose bodies, but no intra synovial disease. The current patient had stage three disease.
X-rays may show loose bodies in the joint but can underestimate the size of the lesion. MRI helps to define the extent of the lesion, identify involvement of other structures such as adjacent marrow, soft tissues, neurovascular structures and differentiating it from other synovial disorders.
Surgical excision is the preferred treatment.  On a clinical basis malignant transformation needs to be considered if there is a rapid recurrence following synovectomy, sudden exacerbation of the symptoms or extension of the process beyond the joint capsule occur. Microscopically features include chondrocytic arrangement in sheets without clustering architecture, a myxoid change in the stroma, necrotic change and rarely mitotic figures. Radiological evidence of bony invasion or soft tissue invasion on MRI should raise suspicion of malignant change recurrence ranges from 3.2% to 22.2%, respectively. Radiotherapy is useful for recurrent lesions and inhibition of FGF-9 has been suggested as nonoperative treatment of primary synovial chondromatosis.
| Acknowledgments|| |
We are thankful to the Superintendent, Government General Hospital, Principal, Kurnool Medical College, Kurnool and other staff members and faculty of the Department of Orthopedics, Kurnool Medical College, Kurnool. We specially thank Dr. O. Sujith Postgraduate in Orthopedics for his contribution to this study.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]