Krishnamurthy Arvind, Singh Shirley Sundar, Majhi Urmila, Ramshankar Vijayalakshmi, Krishnamurthy Arvind
Cancer Institute (WIA), 38, Sardar Patel Rd, Adyar, Chennai, 600036 India.
J Maxillofac Oral Surg. 2016 Jul;15(Suppl 2):378-81. doi: 10.1007/s12663-016-0926-2. Epub 2016 Jun 9.
Solitary fibrous tumors (SFTs) are uncommon spindle-cell tumors of mesenchymal origin initially described in the pleura and subsequently in other extra-pleural sites. These tumors are categorized as tumors of 'intermediate malignancy' under the World Health Organization classification of soft tissue tumors. SFT was virtually non-existent or misdiagnosed until its characteristic features, particularly the strong and diffuse immuno-reactivity to CD 34 were described. Extra-pleural manifestations of SFT, particularly in the head and neck region are rare. Although a number of isolated case reports of orbital SFTs have been described ever since its initial description in 1994, cases of recurrent SFTs have been very few. Recurrences of these tumors following surgery are considered unusual and metastasis exceptional. We describe clinical presentation and the management challenges of recurrent giant orbital SFT in a 15-year old girl along with a brief review of literature.
孤立性纤维性肿瘤(SFTs)是一种罕见的间叶源性梭形细胞肿瘤,最初在胸膜中被描述,随后在其他胸膜外部位被发现。在世界卫生组织软组织肿瘤分类中,这些肿瘤被归类为“中间恶性”肿瘤。在其特征性表现,特别是对CD 34呈强而弥漫性免疫反应被描述之前,SFT实际上并不为人所知或被误诊。SFT的胸膜外表现,尤其是在头颈部区域很少见。自1994年首次描述以来,虽然已经有一些孤立的眼眶SFT病例报告,但复发性SFT病例却非常少。这些肿瘤术后复发被认为不常见,转移则更为罕见。我们描述了一名15岁女孩复发性巨大眼眶SFT的临床表现和治疗挑战,并对相关文献进行简要回顾。