DiLascio J P, Devlin G P, Doyle J L
J Oral Surg. 1981 Feb;39(2):134-6.
A rare case of aggressive fibrous histiocytoma is presented to alert the clinician to the existence of such a lesion and its ability to develop as a perioral soft tissue tumor. The research on these lesions clearly demonstrates the lability of their biologic potential. The clinical characteristics, symptoms, and histiologic makeup are reviewed and further reinforce the conclusion that careful microscopic study and thorough longterm followup to adequate surgical treatment are currently the only effective means in the management of these tumors. Continued reports from clinicians and researchers will perhaps satisfy many questions concerning this curious and potentially destructive and lethal group of lesions.
本文报告一例罕见的侵袭性纤维组织细胞瘤，以提醒临床医生注意此类病变的存在及其作为口周软组织肿瘤发展的可能性。对这些病变的研究清楚地表明了它们生物学潜能的不稳定性。本文回顾了其临床特征、症状和组织学构成，进一步强化了以下结论：目前，仔细的显微镜检查、充分手术治疗后的长期彻底随访是管理这些肿瘤的唯一有效手段。临床医生和研究人员持续发表的报告可能会解答许多关于这类奇特且具有潜在破坏性和致命性病变的问题。
