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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Central Telangiectatic Osteosarcoma of the Mandible in a Paediatric Patient: A Rarity
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Central Telangiectatic Osteosarcoma of the Mandible in a Paediatric Patient: A Rarity

机译:小儿患者下颌骨中央毛细血管扩张骨肉瘤:罕见

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Osteosarcoma (OS) involving the head and neck region is rare and is a diagnostic challenge due to its aggressive nature and varied presentations. Although OS constitute 40% to 60% of all bone tumours, only 10% of these occur in the head and neck region, most commonly in the maxilla and mandible. OS of the jaw bone has a different pattern and behaviour when compared to OS at other anatomic location. It occurs in a more elderly population, less aggressive and usually spreads locally rather than distant metastases. Telangiectatic Osteosarcoma (TOS) of jaws in a paediatric patient are still a very rare variant and till date only two cases have been reported in literature. Radiographic evaluation plays an important role as the clinical symptoms are not specific to the condition. Conventional radiography should always be supplemented by advanced imaging modalities for the diagnosis, which gives a three dimensional assessment and also prevents superimposition of surrounding structures. Early diagnosis and radical surgery are the keys to high survival rates. Herein, we present a third ever reported case of TOS occurring in mandible of a nine-year-old male patient.
机译:涉及头部和颈部区域的骨肉瘤(OS)很少见,由于其侵略性和表现形式多样,因此是诊断难题。尽管OS占所有骨肿瘤的40%至60%,但其中只有10%发生在头部和颈部,最常见于上颌骨和下颌骨。与其他解剖位置的OS相比,颌骨的OS具有不同的模式和行为。它发生在年龄较大的人群中,侵略性较低,通常在局部而不是远处转移。儿科患者颌骨的毛细血管扩张骨肉瘤(TOS)仍然是非常罕见的变异,迄今为止,文献中仅报道了两例。放射学评估起着重要作用,因为临床症状并非特定于该疾病。常规放射线照相应始终以先进的成像方式进行诊断,以进行三维评估,并防止周围结构重叠,从而对诊断进行补充。早期诊断和根治性手术是高存活率的关键。在此,我们介绍了第三例有报道的9岁男性患者下颌骨发生TOS的情况。

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