下颌骨肉瘤样癌1例报告及文献复习

K. Benali, T. Kebdani, K. Hassouni, S. Majjaoui, H. Kacemi, N. Benjaafar
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引用次数: 0

摘要

背景:肉瘤样癌是一种罕见的双期恶性肿瘤,具有上皮和间质成分。鉴于其组织学上的特殊性,这种肿瘤的诊断对病理学家和外科医生来说仍然是一个挑战。摘要下颌骨肉瘤样癌是一种非常罕见且具侵袭性的肿瘤。迄今为止,文献中仅报告了零星病例。目的:报道一例罕见的侵袭性下颌肉瘤样癌的根治性手术和辅助放化疗,并讨论相关文献。病例报告:我们报告一例罕见的下颌肉瘤样癌,发生在一名34岁的女性。治疗包括根治性手术和阳性边缘的再切除,辅助放射治疗(66 Gy, 33个部分,同时使用体积调制弧线治疗进行综合增强)和顺铂同步化疗。肿瘤表现出侵袭性和高转移潜力,可引起肿瘤复发和广泛的肺转移。结论:下颌骨肉瘤样癌是一种极为罕见的恶性肿瘤,易局部复发、远处转移。治疗包括根治性手术和辅助放化疗,尽管结果和预后可能较差。
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Sarcomatoid Carcinoma of the Mandible: A Case Report and Literature Review
Background: Sarcomatoid carcinoma is a rare biphasic malignancy with an epithelial and mesenchymal component. Given its histological particularity, the diagnosis of this tumor still represents a challenge for pathologists and surgeons. Sarcomatoid carcinoma of the mandible is a very rare and aggressive entity. To date, only sporadic cases have been reported in the literature. Aim: To report a rare case of aggressive mandibular sarcomatoid carcinoma treated with radical surgery and adjuvant chemoradiation, and discuss the re-lated literature. Case Report: We introduce a rare case of mandibular sarcomatoid carcinoma occurring in a 34-year-old woman. Treatment consisted of radical surgery and re-excision for positive margins, adjuvant radiation therapy (66 Gy in 33 fractions in simultaneous integrated boost delivered using Volumetric Modulated Arc Therapy) and Cisplatin-based concurrent chemotherapy. The tumor displayed aggressive behavior and high metastatic po-tential, causing tumour recurrence and extensive lung metastasis. Conclu-sion: Sarcomatoid carcinoma of the mandible is an extremely rare malignant entity, with a high tendency for local recurrence, distant metastasis. Treatment involves radical surgery and adjuvant chemoradiation, although the outcome and prognosis might be poor.
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