Huge Osteosarcoma of Mandible in a 16 Year Girl: A Case Report

Prabhat Ch, R. Thakur, P. Jaiswal, S. Sharma, S. Basnet, KrishnaNagarkoti, Sudeep Amatya
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Abstract

Osteosarcomas are primary malignant bone tumors in which mesenchymal cells produce osteoid. It is generally the most common malignant bone neoplasm, although lesions of the jaw are uncommon. Osteosarcoma of the Jaw (JOS) presents a lower incidence of metastasis and a better prognosis than osteosarcoma of the long bones. However, patients with JOS can exhibit advanced tumors, mainly when early diagnosis is not performed. This article reports on a case of an advanced osteosarcoma of the mandible. A 16-year-old lady came for evaluation and treatment of lower jaw mass. The patient had been noticing loose teeth and progressively enlarging mass since 3 months. Computed tomography showed large heterogenous lesion measuring 8.4 × 6.8 cm arising from mandible with cortical destruction and periosteal reaction. She had undergone incisional biopsy which revealed ill circumscribed subepithelium tumor with alternating areas of chondromyxoid and fibrocellular components, foci of osteoid formation, areas of ischemia type of necrosis, abscess formation and established the diagnosis as osteosarcoma of bone chondroblastic type. The patient was then recommended for oncologic treatment with 2 cycles of pre-operative chemotherapy. She received 1 cycle NACT (adriamycin+cisplastin), but as the disease was progressing quickly, so she was referred to our centre and underwent surgery.
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16岁女孩下颌骨巨大骨肉瘤1例
骨肉瘤是由间充质细胞产生类骨细胞的原发性恶性骨肿瘤。它通常是最常见的恶性骨肿瘤,虽然病变的颌骨是罕见的。颌骨骨肉瘤(JOS)比长骨骨肉瘤转移发生率低,预后好。然而,JOS患者可表现为晚期肿瘤,主要是在未进行早期诊断的情况下。本文报告一例晚期下颌骨骨肉瘤的病例。一位16岁的女士来评估和治疗下颚肿块。自3个月以来,患者一直注意到牙齿松动和肿块逐渐扩大。计算机断层扫描显示,下颌骨出现8.4 × 6.8 cm的巨大异质病变,伴有皮质破坏和骨膜反应。患者行切口活检,发现界限不清的上皮下肿瘤,伴有软骨黏液样和纤维细胞成分的交替区,类骨形成灶,缺血型坏死区,脓肿形成区,诊断为骨成软骨型骨肉瘤。然后建议患者进行2个周期的术前化疗。她接受了1个周期的NACT(阿霉素+顺铂)治疗,但由于病情进展迅速,因此她被转介到我们的中心并接受了手术。
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