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https://hdl.handle.net/11499/30282
Title: | A rare rib lesion due to parosteal osteosarcoma: a case report 11 medical and health sciences 1112 oncology and carcinogenesis | Authors: | Tozum, H. Aydemir, Ahmet Nadir Demiroglu, M. Ozkan, K. Ceyran, A.B. Klllc, B. |
Keywords: | Chest wall reconstruction Parosteal osteosarcoma adult Article bone biopsy case report clinical article computer assisted tomography female fibroblast flail chest follow up histopathology human human tissue laboratory test medical history osteoblast osteosarcoma parosteal osteosarcoma physical examination priority journal rib malformation rib resection segmentectomy thorax radiography thorax wall defect thorax wall reconstruction whole body scintiscanning young adult bone plate bone tumor diagnostic imaging pathology procedures reconstructive surgery rib surgical mesh thorax wall treatment outcome x-ray computed tomography Bone Neoplasms Bone Plates Female Humans Osteosarcoma, Juxtacortical Reconstructive Surgical Procedures Ribs Surgical Mesh Thoracic Wall Tomography, X-Ray Computed Treatment Outcome Young Adult |
Publisher: | BioMed Central Ltd. | Abstract: | Introduction: Masses which develop on the surface of the rib bones are rare. The differential diagnosis includes benign and malignant lesions. Case presentation: A 23-year-old European woman presented at an out-patient clinic with a 9-month history of a painless swelling on the right posterolateral side of her chest wall. The case reported here is of a very rarely seen parosteal osteosarcoma of the rib that was treated with wide resection and chest wall reconstruction. There was no evidence of local recurrence or distal metastasis after a 1-year follow-up. Conclusion: Parosteal osteosarcoma is a locally aggressive malignant tumor, and resection with a wide margin is the most appropriate treatment. Correct diagnosis of parosteal osteosarcoma is challenging for an orthopedic surgeon. Although rare, in the differential diagnosis of lesions located on the ribs, parosteal osteosarcoma should be considered and a systematic diagnostic approach should be taken. © 2019 The Author(s). | URI: | https://hdl.handle.net/11499/30282 https://doi.org/10.1186/s13256-018-1958-7 |
ISSN: | 1752-1947 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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