1/17. Synovial chondromatosis of the elbow.Synovial chondromatosis is an uncommon disorder with rare occurrence in the elbow. case reports in the literature for elbow synovial chondromatosis have described presenting symptoms secondary to peripheral nerve compressions or localized bursitis. We discuss a case of synovial chondromatosis of the elbow that presented as an isolated soft-tissue mass over the radial head-more suggestive of a soft-tissue tumor than of synovial chondromatosis.- - - - - - - - - - ranking = 1keywords = soft (Clic here for more details about this article) |
2/17. Synovial chondroma of the ankle in a young child after recent trauma: CT and MR features.We report a case of synovial chondroma of the left ankle in an 11-year-old boy presenting with soft tissue swelling after recent trauma. The noncalcified or nonossified intraarticular chondroma arising from metaplastic synovium has characteristic imaging appearance on computed tomography (CT) and magnetic resonance imaging (MRI). A lobulated mass of fluid-like density and signal intensity along with internal septa are characteristic features on CT and MRI. The knowledge of CT and MRI features of noncalcified or nonossified synovial chondroma is important to distinguish from the simple or complicated effusion, hemarthrosis, or other synovial process.- - - - - - - - - - ranking = 0.5keywords = soft (Clic here for more details about this article) |
3/17. Multiple giant synovial chondromatosis of the knee.This report describes an unusual presentation of monoarticular synovial chondromatosis of the knee. In this case, multiple giant chondroid nodules presented as a painless soft tissue mass. There was no calcification but bony erosion was seen on MR scan. Such lesions may mimic a malignant neoplasm and pose a diagnostic problem.- - - - - - - - - - ranking = 0.5keywords = soft (Clic here for more details about this article) |
4/17. Acral synovial chondrosarcoma.Acral chondrosarcoma is rare. Synovial chondrosarcoma is even rarer. Synovial chondrosarcoma arising without evidence of pre-existing or concurrent synovial chondromatosis is exceedingly rare. We present a case of acral synovial chondrosarcoma involving both sides of the metacarpophalangeal joint of the thumb in a 69-year-old man. Radiographically, the lesion mimicked gout. On MR imaging, the lobulated contours of the soft tissue mass suggested synovial chondromatosis. Histological examination revealed a chondrosarcoma, which on the basis of imaging findings we present as having arisen from the synovium. The tumor invaded a portion of the cartilage of the metacarpophalangeal joint and equally destroyed the bones of the distal metacarpal and base of the proximal phalanx of the thumb, while sparing the bony joint surfaces.- - - - - - - - - - ranking = 0.5keywords = soft (Clic here for more details about this article) |
5/17. Condylar hyperplasia associated to synovial chondromatosis of the temporomandibular joint: a case report.Condylar hyperplasia is a slowly developing malformation of the mandible, with elongation of the mandibular neck, that generally results in facial asymmetry. Synovial chondromatosis is a benign chronic disorder characterized by the formation of multiple small nodules of hyaline cartilage as a result of metaplasia of the synovial connective tissue. It affects mostly the large joints, particularly the knee, hip, elbow and ankle. The temporomandibular joint (TMJ) is rarely affected. The case of a 42-year-old male with a history of left preauricular pain and swelling and deviation of the mandible to the left upon opening the mouth is presented. Computed tomography disclosed hyperplasia of the left condyle with loose radiopaque bodies within the joint cavity. The left TMJ was subject to open surgery, which included resection of four loose bodies and a remodeling condylectomy. The histopathological study confirmed the diagnosis of condylar hyperplasia and chondromatosis of the left TMJ.- - - - - - - - - - ranking = 2.5126325271298keywords = connective (Clic here for more details about this article) |
6/17. Synovial chondromatosis of the elbow presenting as a soft tissue tumour.Synovial chondromatosis of the elbow is not common. bursitis, neurocompression and locking are the usual symptoms. We describe a case which was initially thought to be a soft tissue tumour, i.e. a synovial sarcoma.- - - - - - - - - - ranking = 2.5keywords = soft (Clic here for more details about this article) |
7/17. Synovial chondromatosis of the hip: a case report and clinicopathologic study.Primary synovial chondromatosis (PSC) is a rare, usually monoarticular disorder of synovial joints. PSC is characterised by the formation of osteocartilaginous nodules in the synovial connective tissue. We report the case of a 32-year-old male with PSC of the left hip. At clinical examination abduction of the left hip was limited and rotation was painful. Ultrasound examination of the hip revealed joint effusion and multiple hyperechogenic foci due to distal acoustic shadowing. Plain radiographs showed a slight soft tissue swelling around the femoral neck and multiple round or ovoid calcifications of a uniform size. MRI revealed a large joint effusion with multiple small filling defects. Open total synovectomy was performed after dislocation of the femoral head. The diagnosis of PSC was confirmed by histological examination of the excised material. The majority of cells failed to exhibit any staining for cerb B-2 and ki-67. None of the sections showed more than 5% labelling for dna-fragmentation proven by terminal deoxytransferase-mediated dUTD nick-end labeling (TUNEL), and all were completely non-reactive for p53 as well. In conclusion, immunohistochemical analysis suggests that in this case PSC originated from metaplasia and not from a proliferative process. After two years, the patient was free of symptoms and radiological control did not show evidence of recurrence or femoral head necrosis. Physical findings, diagnosis, histological features and management of PSC are discussed.- - - - - - - - - - ranking = 3.0126325271298keywords = connective, soft (Clic here for more details about this article) |
8/17. Synovial chondromatosis of the acromioclavicular joint.A 53-year-old woman presented with swelling of 3 years' duration on the right anterior chest wall. A radiograph showed coarse calcifications around the subclavicular region and erosion of the ipsilateral acromioclavicular joint. Computed tomography also showed calcifications in soft tissue. magnetic resonance imaging revealed a tumor around the clavicle extending to the anterior aspect of chest wall, which had low signal intensity on T1-weighted imaging and high signal intensity on T2-weighted imaging. The histologic findings were of a hyaline cartilage-like mass consisting of mature chondrocytes and an extracellular matrix. The histologic diagnosis of synovial chondromatosis was made. The present case is unusual in respect of the location and size of the tumor.- - - - - - - - - - ranking = 0.5keywords = soft (Clic here for more details about this article) |
9/17. Synovial osteochondromatosis of the ankle: MR findings.The authors present a case of primary synovial osteochondromatosis of the ankle, as demonstrated by magnetic resonance (MR). ankle involvement by osteochondromatosis is unusual. The characteristic MR findings are: target appearance of some loose bodies with a low intensity peripheral rim and a center isointense to the soft tissues on T1-weighted images, which remain unchanged on T2-weighted images. Conversely, other loose bodies were characterized by homogeneous hyperintensity close to the bone marrow on T1-weighted images, with loss of signal on T2-weighted images. The authors believe that these findings are quite pathognomonic of a long-standing synovial osteochondromatosis.- - - - - - - - - - ranking = 0.5keywords = soft (Clic here for more details about this article) |
10/17. A case of tenosynovial chondromatosis with tophus-like deposits.Tenosynovial chondromatosis has not been well recognized because of its rarity, but it is clinically important because of its high rate of recurrence. We report here a case of tenosynovial chondromatosis with deposits of crystalline material that appeared to be sodium urate (gouty tophi). A 37-year-old Japanese man was admitted because of a hard mass in his left third finger. He had undergone surgery at the same anatomical site four and seven years previously. The roentgenogram revealed a soft tissue mass in the flexor aspect of the proximal phalanx. At operation, the tumor was found to have arisen in the tendon sheath. Histopathological examination showed that the tumor was composed of well-defined, multiple, cartilaginous nodules that were surrounded by tenosynovial tissue. A few of the nodules were calcified. The chondrocytes had mild atypia, and were immunopositive for S-100 protein. A diagnosis of tenosynovial chondromatosis was made. The nodules also contained crystalline deposits, which bore a histological resemblance to gouty tophi. We were unable to define the exact nature of these deposits even by transmission electron microscopy and electron roentgenographic microanalysis. Crystalline deposits in chondromas of soft tissue have been reported but not in tenosynovial chondromatosis.- - - - - - - - - - ranking = 1keywords = soft (Clic here for more details about this article) |
| | Next -> |