上颌血管肉瘤1例报告并文献复习

Q3 Dentistry
Kamdem Benedikta , Sala Nathalie , Broome Martin , May Laurence
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引用次数: 0

摘要

血管肉瘤是一种罕见的侵袭性恶性间充质瘤,起源于内皮细胞,仅占软组织肉瘤的2%。虽然主要影响软组织和皮肤,但在口腔发生的情况非常罕见(1.6%)。我们提出的情况下,一个78岁的妇女与结节性牙龈病变最初怀疑为鳞状细胞癌。尽管上颌切除术后的手术过程顺利,但组织学检查显示血管肉瘤。讨论强调了诊断的挑战,由于其不同的临床和组织学表现,往往模仿其他病变。治疗包括完全手术切除,然后辅助化疗和放疗。然而,预后仍然很差,具有高复发率和转移潜力。我们的病例强调了通过全面的临床、放射学和组织学评估准确诊断的重要性,强调了早期发现和多学科管理的必要性,以改善血管肉瘤患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maxillary angiosarcoma: a case report and literature review
Angiosarcoma is a rare and aggressive malignant mesenchymal neoplasia developing from endothelial cells, comprising only 2 % of soft tissues sarcomas. While primarily affecting soft tissues and skin, its occurrence in the oral cavity is exceptionally rare (1.6 %). We present the case of a 78-year-old woman with a nodular gingival lesion initially suspected as squamous cell carcinoma. Despite an uneventful postoperative course following maxillectomy, the histological examination revealed angiosarcoma. Discussion highlights the diagnostic challenges due to its varied clinical and histological presentation, often mimicking other lesions. Treatment involves complete surgical excision, followed by adjuvant chemotherapy and radiotherapy. However, the prognosis remains poor, with a high recurrence rate and metastatic potential. Our case underscores the importance of accurate diagnosis through comprehensive clinical, radiological, and histological evaluation, emphasizing the need for early detection and multidisciplinary management to improve outcomes in angiosarcoma patients.
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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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