[Rhabdomyosarcoma of soft palate. A case on purpose].

F Arias Marzán, M De Bonis Redondo, F Redondo Ventura, L Betancor Martínez, M Sanginés Yzzo, J Arias Marzán, C De Bonis Braun, V Zurita Expósito, F Reig Ripoll, G De Lucas Carmona
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引用次数: 0

Abstract

The rabdomiosarcoma (RMS) are infrequent tumors. They are principally described in infancy and located in 35% of the cases in head and neck. The nasopharynx localisation is relatively rare, being in these cases the tongue, palate and oral mucosa the preferent places of establishment. Classically the patient presented very low standard healing with surgery and radiotherapy. The introduction in the middle 70 of systematic chimiotherapy as complementary treatment, improved the survival rate in large scale. In this article the case of an adolescent patient, who presented a RMS at the level of the soft palate, the diagnostic procedure and the therapeutic decision adopted, after revision of the last studies at this respect, are described.

软腭横纹肌肉瘤。[故意为之]。
rabdomiosarcoma (RMS)是一种罕见的肿瘤。它们主要发生在婴儿期,位于头颈部的病例占35%。鼻咽部定位是相对罕见的,在这些情况下,舌头,上颚和口腔粘膜是首选的建立位置。通常情况下,患者的手术和放疗治疗标准很低。70年代中期引入系统化疗作为辅助治疗,大规模提高了生存率。在这篇文章中,一个青少年患者的情况下,谁提出了一个RMS在软腭水平,诊断程序和治疗决定采用,在这方面的最后研究修订后,描述。
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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