ArticleQuantitative imaging in medicine and surgery2022
Clinical and imaging features of 112 patients with irregular and flat bone osteosarcoma.
Article in Quantitative imaging in medicine and surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed, 8 citations in OpenAlex.
- Primary temporal bone osteosarcoma presenting as a parotid tumor: A case report with diagnostic challenges.Radiology case reports · 2025Article
- Monitoring early responses to neoadjuvant chemotherapy and the factors affecting neoadjuvant chemotherapy responses in primary osteosarcoma.Quantitative imaging in medicine and surgery · 2023Article
- Development of a 3D-printed pelvic CT phantom combined with fresh pathological tissues of bone tumor.Quantitative imaging in medicine and surgery · 2022Article
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9 authors at 6 institutions in 2 countries.
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Abstract
Background: This study evaluated the clinical characteristics and imaging findings of 112 patients with irregular and flat bone osteosarcoma (IFBO). Methods: The age, gender, location, tumor size, density and signal intensity, osteoid matrix, periosteal reaction, and histological subtypes were analyzed for 112 patients with IFBO. Results: A total of 112 patients with IFBO, including 64 males and 48 females, with a mean age of 34.8 years were enrolled in this study. Over half of the tumors (54.5%) were detected in the craniofacial region and the skull (24 in the maxilla bone, 17 in the mandible bone, 11 in the sphenoid bone, 7 in the temporal bone, 1 in the frontal bone, and 1 in the occipital bone). Other tumor locations included the pelvic region (20.5%; 20 in the ilium and 3 in the pubis), the chest (18.8%; 11 in the scapula, 7 in the ribs, and 3 in the clavicle), and the vertebrae (6.3%; 3 in the thoracic spine, 2 in the lumbar spine, 1 in the sacrum, and 1 in the cervical spine). Transarticular extension occurred in 11 of the 23 pelvic cases (47.8%), primarily involving the sacroiliac joint (90.9%; 10 of 11). Six cases (6/7; 85.7%) of vertebral osteosarcoma arose from the transverse process and the pedicle, and 1 (1/7; 14.3%) arose from the sacral tuberosity and the ala, with partial vertebral body involvement. Additionally, 27 patients (24.1%) presented with secondary osteosarcoma related to prior radiotherapy, and 2 (1.8%) were associated with osteoblastoma and fibrous dysplasia. Histological examination revealed high-grade tumors in 88 (78.6%) cases. The tumors presented as soft-tissue masses with a diameter of 7.5±3.2 cm. A total of 91 patients underwent X-ray examination and/or computed tomography (CT) examinations. The osteoid matrix was detected in 84 patients (84/91;92.3%). A periosteal reaction was detected in 56 cases (56/91; 61.5%), including a lamellar periosteal reaction in 10 patients (11.0%) and a spiculated periosteal reaction in 46 cases (50.5%). All 74 cases who underwent magnetic resonance imaging (MRI) examinations presented with heterogeneous masses in the surrounding soft tissue. Enhancement was homogenous in 12 cases (18.5%) and heterogeneous in 53 cases (81.5%). Peripheral rim enhancement was observed in 10 cases (13.5%). Conclusions: IFBO should be considered when diagnosing patients over 30 years of age who exhibit osteoid matrix in bone lesions. Maxillofacial osteosarcoma is commonly associated with a history of radiation exposure. Pelvic osteosarcoma is more likely to invade the sacroiliac joint. Vertebral osteosarcoma frequently arises in the transverse process and pedicle, with partial body involvement.
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