超越极限:下颌骨进行性平滑肌肉瘤1例

M. Ordinario, May N. Sabando, Anna Marie Pascual Panganiban
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引用次数: 0

摘要

平滑肌肉瘤(LMS)是一种罕见的恶性肿瘤,起源于平滑肌。它占头颈部所有肉瘤的3%到10%。此外,由于口腔和颌骨的平滑肌很少,因此在这些区域极为罕见。梭形细胞有明显的平滑肌分化、明显的异型性特征以及免疫组化(IHC)染色中肌动蛋白和desmin的存在是LMS的特征。常见的扩散模式与其他肉瘤相似,累及肺部,很少累及淋巴管。手术、放疗和化疗已被描述为标准的治疗形式。由于局部、区域和远处转移率高,预后通常较差。在本文中,我们提出了一个23岁的女性谁提出了下颌骨平滑肌肉瘤的情况。她仍然有良好的表现状态,并能够在她去世前接受多种治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond Limits: A Case of Progressive Leiomyosarcoma of the Mandible
Leiomyosarcoma (LMS) is a rare malignancy which develops from the smooth muscles. It constitutes about 3 to 10% of all sarcomas in the head and neck area. Furthermore, it is extremely rare in the area of the mouth and jaws due to the rarity of smooth muscle in these areas. Spindle cells with visible smooth muscle differentiation, distinct features of atypia and presence of actin and desmin in Immunohistochemical (IHC) stains are characteristic of LMS. The common pattern of spread is similar with other sarcomas, involving the lung and rarely the lymphatics. Surgery, Radiotherapy and Chemotherapy have been described as standard forms of management. The prognosis is usually poor as rate of local, regional and distant metastasis is high. In this paper, we present a case of a 23 year-old female who presented with Leiomyosarcoma of the mandible. She remained to have good performance status and was able to undergo multiple lines of treatment for progressive disease prior to her demise.
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