Tenna S, Poccia I, Cagli B, Aveta A, Manzo M J, Persichetti P
Campus Bio-Medico University of Rome, Division of Plastic and Reconstructive Surgery, Via Alvaro del Portillo 200, 00128 Rome, Italy.
Int J Surg Case Rep. 2012;3(5):177-80. doi: 10.1016/j.ijscr.2012.01.009. Epub 2012 Feb 11.
The solitary fibrous tumor (SFT) is a rare soft tissue tumor with a substantially benign clinical behavior. However, malignant neoplasms with local recurrence or distant metastases have been reported.
The authors present a case of an aggressive SFT of the leg, in a 55 years old Caucasian man. Radiological, histological and molecular findings are reported. The differential diagnosis, therapy and outcome of this rare tumor are also discussed.
An extensive review of literature showed SFT's clinical behavior as substantially benign, anyway aggressive or malignant neoplasms have been described. The potential risk of local recurrence and distant metastasis thus suggests wide surgical resection and careful long-term follow-up. Differential diagnosis may be quite laborious as SFT can mimic a variety of benign and malignant mesenchymal tumors; immunohistochemical analysis for CD34, CD99, vimentin and bcl-2 is then mandatory.
Our clinical experience confirmed that SFT may have an aggressive behavior, however, conservative surgical treatment may be successful in the long term.
孤立性纤维瘤(SFT)是一种罕见的软组织肿瘤,临床行为基本为良性。然而,已有局部复发或远处转移的恶性肿瘤报道。
作者报告一例55岁白种男性腿部侵袭性SFT病例。报告了影像学、组织学和分子学检查结果。还讨论了这种罕见肿瘤的鉴别诊断、治疗及预后。
广泛的文献综述表明SFT的临床行为基本为良性,但也有侵袭性或恶性肿瘤的描述。局部复发和远处转移的潜在风险提示需进行广泛手术切除并仔细长期随访。由于SFT可模仿多种良性和恶性间叶性肿瘤,鉴别诊断可能相当费力,因此必须进行CD34、CD99、波形蛋白和bcl-2的免疫组化分析。
我们的临床经验证实SFT可能具有侵袭性行为,然而,保守手术治疗长期来看可能成功。