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Osteosarcoma of the jaws: a review of literature and a case report on synchronous multicentric osteosarcomas

机译:颌骨骨肉瘤:文献复习和同步多中心骨肉瘤病例报告

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Background In the head and neck region, osteosarcoma is the most common primary malignant bone tumor, representing 23% of total head and neck malignancies. Osteosarcomas of the jaws are nevertheless rare lesions, representing only 2 to 10% of all osteosarcomas. This report reviews a single-center histopathology experience with craniofacial osteosarcomas, and reports the management of unusually large synchronous mandibular and maxillary osteosarcomas in a patient. Patients and methods A search of the hospital pathology database for specimens with a histological diagnosis of osteosarcomas submitted between July 1992 and May 2011 was made. A chart review of a patient with large synchronous maxillary and mandibular osteosarcomas was performed, and is reported. Case presentation A 21-year-old African man with large maxillary and mandibular tumors under palliative care presented with increasing difficulties with eating, speech, and breathing. Surgical debulking was performed, with histology confirming synchronous osteosarcomas of the mandible and maxilla. The patient is well after one year, with no evidence of recurrence, having undergone no further treatment. Conclusion Osteosarcomas of the jaw remain enigmatic, and a number of difficulties related to their diagnosis and treatment are yet to be resolved. True synchronous multicentric osteosarcomas of the jaws are extremely rare but, like other osteosarcomas of the jaws, have a favorable outcome, and palliative resection of such lesions, though challenging, can therefore lead to an enormously improved quality of life and self-image, and may even offer the opportunity for cure.
机译:背景技术在头颈部区域,骨肉瘤是最常见的原发性恶性骨肿瘤,占头颈部恶性肿瘤总数的23%。然而,颌骨肉瘤是罕见的病变,仅占所有骨肉瘤的2%至10%。该报告回顾了颅面部骨肉瘤的单中心组织病理学经验,并报告了患者异常大的同步下颌骨和上颌骨肉瘤的治疗。患者和方法在医院病理数据库中搜索1992年7月至2011年5月之间提交的具有骨肉瘤组织学诊断的标本。进行了图表回顾,该患者患有上颌骨和下颌骨同步大骨肉瘤,并已报告。病例介绍一名21岁的非洲男子在姑息治疗下患有上颌和下颌大肿瘤,其进食,言语和呼吸困难日益增加。进行了手术切除,其组织学证实了下颌骨和上颌骨同时发生骨肉瘤。病人在一年后康复良好,没有复发的迹象,也没有接受进一步的治疗。结论颌骨骨肉瘤仍是难以捉摸的,其诊断和治疗相关的许多难题尚待解决。真正的颌骨同步多中心骨肉瘤极为罕见,但与其他颌骨骨肉瘤一样,具有良好的预后,尽管姑息性切除这些病变,尽管具有挑战性,但可以大大改善生活质量和自我形象,并且甚至可以提供治愈的机会。

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