Clinical and morphological observation of a 19-year-old patient with alveolar rhabdomyosarcoma of the head and neck region

Yu. E. Ryabukhina, A. Fedenko, P. A. Zeynalova, O. L. Timofeeva, F. М. Abbasbeyli, D. Chekini, A. Mudunov, A. Batsev, O. V. Sinitsyna, A. G. Zhukov, L. A. Shestakova, G. Allakhverdieva, I. Yurichev
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Abstract

Alveolar rhabdomyosarcoma (ARMS) is an aggressive primitive tumor with limited differentiation of rhabdomyoblasts. Primarily, it occurs in children and teens under 15 years of age in the head and neck region (in 40 % of cases). In patients older than 19-20 years, ARMS is significantly less common and is localized primarily on the limbs, while head and neck region is affected in about 24 % of all cases, involvement of the orbit in the tumor process is very rare. ARMS progression in adults is more aggressive than in children, and prognosis is more unfavorable due to development of regional and distant metastases at the time of diagnosis. Hence, selection of antitumor therapy is limited to drug treatment. Use of multimodal approach to therapy allows to improve treatment outcomes and increase quality of life in patients with ARMS.
1例19岁头颈部肺泡横纹肌肉瘤的临床及形态学观察
肺泡横纹肌肉瘤(ARMS)是一种侵袭性的原始肿瘤,横纹肌母细胞分化有限。它主要发生在头颈部15岁以下的儿童和青少年(占40%的病例)。在年龄大于19-20岁的患者中,ARMS明显不常见,主要局限于四肢,而头颈区域约占所有病例的24%,在肿瘤过程中累及眼眶非常罕见。成人的ARMS进展比儿童更具侵袭性,由于在诊断时发生区域和远处转移,预后更不利。因此,抗肿瘤治疗的选择仅限于药物治疗。使用多模式治疗方法可以改善ARMS患者的治疗效果和提高生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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