Beeson W H, Singer M I, Lingeman R E
Laryngoscope. 1980 Aug;90(8 Pt 1):1336-43.
Fibrosarcoma is uncommon in the head and neck and constitutes less than 1% of malignancies and approximately 6% of the soft tissue sarcomas. Congenital fibrosarcomas are characterized by rapid proliferation and frequent local recurrence following excision. Unlike other sarcomas, metastasis is a rare event. The literature contains less than 50 cases of congenital, solitary fibrosarcoma, with none occurring in the oral cavity. This paper describes a unique case of fibrosarcoma in the oral cavity of a neonate. A 12 month follow-up is provided with an analysis of the histopathology including electron microscopy. The spectrum of fibroproliferative lesions in the pediatric patient is reviewed, and the evaluation and treatment modalities applicable to this age group are outlined.
纤维肉瘤在头颈部并不常见,占恶性肿瘤的比例不到1%,约占软组织肉瘤的6%。先天性纤维肉瘤的特点是生长迅速,切除后局部复发频繁。与其他肉瘤不同,转移是罕见事件。文献中报道的先天性孤立性纤维肉瘤病例不到50例,口腔内尚未见报道。本文描述了1例新生儿口腔纤维肉瘤的罕见病例。提供了12个月的随访情况,并对包括电子显微镜检查在内的组织病理学进行了分析。回顾了儿科患者纤维增生性病变的范围,并概述了适用于该年龄组的评估和治疗方式。