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Rare Adult Masseteric Rhabdomyosarcoma and a Review of the Literature

机译:成人罕见的咬肌横纹肌肉瘤及其文献复习

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摘要

Background: Rhabdomyosarcomas (RMSs) are a group of soft-tissue malignant tumors which derive from primitive skeletal muscle tissue that mainly affect children and adolescents. RMSs are very rare in adults, where they are usually located in the extremities. Case Presentation: A previously healthy 32-year-old male presented at our ENT (ear, nose and throat) outpatient clinic after experiencing a parotid region swelling for 2 months. The patient was treated surgically by excising the mass and by modified radical ipsilateral neck dissection. Histological and immunohistochemical examination indicated masseteric alveolar RMS with lymphatic metastasis. The patient received radiochemotherapy, and he is still alive with no evidence of disease spread 1 year after diagnosis. Conclusion: This is the first case of a masseter alveolar RMS to be reported in the literature in a patient older than 25 years; it highlights the broad spectrum of neoplasms that cause parotid region swellings and the importance of considering rare tumors during differential diagnosis.
机译:背景:横纹肌肉瘤(RMS)是一组软组织恶性肿瘤,其起源于主要影响儿童和青少年的原始骨骼肌组织。 RMS在成年人中非常罕见,成年人通常位于四肢。病例介绍:一名先前健康的32岁男性在经历腮腺区域肿胀2个月后在我们的耳鼻喉科(耳鼻喉)门诊就诊。通过切除肿物和改良的同侧颈清扫术对该患者进行了手术治疗。组织学和免疫组织化学检查显示有咬合的肺泡RMS伴淋巴转移。患者接受了放射化学疗法,他仍然活着,没有任何证据表明在诊断后1年内有疾病扩散。结论:这是文献中报道的25岁以上患者的咬肌齿槽RMS的第一例。它强调了引起腮腺区域肿胀的广泛肿瘤以及在鉴别诊断中考虑罕见肿瘤的重要性。

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