Suppr超能文献

单骨型骨纤维异常增殖症的恶性转化:10例患者的临床特征、影像特征、治疗结果及文献复习

Malignant transformation in monostotic fibrous dysplasia: clinical features, imaging features, outcomes in 10 patients, and review.

作者信息

Qu Nan, Yao Weiwu, Cui Xiaojiang, Zhang Huizhen

机构信息

From the Department of Radiology (NQ, WY), Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China; Samuel Oschin Comprehensive Cancer Institute (XC), Cedars-Sinai Medical Center, Los Angeles, CA; and Department of Pathology (HZ), Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Medicine (Baltimore). 2015 Jan;94(3):e369. doi: 10.1097/MD.0000000000000369.

Abstract

Malignant transformation in fibrous dysplasia (FD) is uncommon. The purpose of this study was to investigate clinical and imaging features, and outcomes of malignant transformation in monostotic FD.Data for 10 pathologically confirmed malignant transformations in monostotic FD from January 2005 to December 2013 were retrospectively reviewed. Patient data were recorded, and radiographs (n = 10), computed tomography (CT) (n = 5), magnetic resonance (MR) (n = 4), and bone scintigrams (n = 10) were evaluated for lesion location, margin, cortical destruction, marrow involvement, periosteal reaction, and soft tissue mass by 2 musculoskeletal radiologists with agreement by consensus. Clinical features, management, and prognosis were also analyzed for each of the 10 cases.There were 8 male and 2 female patients (mean age 46.5 ± 15.9 years). The affected sites were the femur (n = 4), humerus (n = 2), tibia (n = 3), and ilium (n = 1). Five cases had received previous surgery and 5 cases had no history of surgery. No patients had been given prior irradiation treatment. For the 5 cases with surgery, radiographs and CT showed purely osteolytic lesions with poor margination in the curettage area (n = 5), cortical destruction (n = 5), obvious soft tissue mass (n = 1), and mineralization (n = 2). For the 5 cases without surgery, radiographs and CT identified poorly marginated, osteolytic lesions within or near the area with "ground-glass" opacity (n = 4), cortical erosion (n = 4), and mineralization (n = 2). Magnetic resonance imaging (MRI) also identified lesions with heterogeneous signal intensity and pronounced enhancement. Bone scintigraphy revealed eccentric increased uptake of radionuclide in monostotic lesion (n = 10). Pathology reports revealed osteosarcoma (n = 7), fibrosarcoma (n = 2), and malignant fibrous histiocytoma (MFH) (n = 1). At the end of the study, 1 patient died from tumors, 1 patient was alive with lung metastasis, 1 patient experienced recurrence, and 7 patients were alive without recurrence.Patients with FD and a history of surgery should be followed up, for the osteolytic lesions in the operative areas strongly indicate the malignant transformation. The radiographic feature of FD-related malignancies is poorly marginated, mineralized, and osteolytic lesions with cortical destruction. Further investigations are needed to explore the pathogenesis of malignancies in FD and to establish optimal therapeutic strategies.

摘要

骨纤维发育不良(FD)的恶变并不常见。本研究旨在探讨单发性FD恶变的临床和影像学特征及转归。回顾性分析2005年1月至2013年12月间10例经病理证实的单发性FD恶变患者的数据。记录患者资料,并由2名肌肉骨骼放射科医生对X线片(n = 10)、计算机断层扫描(CT)(n = 5)、磁共振成像(MR)(n = 4)和骨闪烁显像(n = 10)进行评估,就病变部位、边界、皮质破坏、骨髓受累、骨膜反应和软组织肿块达成共识。对这10例患者的临床特征、治疗及预后也进行了分析。

患者中男性8例,女性2例(平均年龄46.5±15.9岁)。受累部位包括股骨(n = 4)、肱骨(n = 2)、胫骨(n = 3)和髂骨(n = 1)。5例曾接受过手术,5例无手术史。所有患者均未接受过放疗。对于5例接受过手术的患者,X线片和CT显示刮除区域内为单纯溶骨性病变,边界不清(n = 5)、皮质破坏(n = 5)、有明显软组织肿块(n = 1)及矿化(n = 2)。对于5例未接受过手术的患者,X线片和CT显示在“磨玻璃”样密度影区域内或其附近有边界不清的溶骨性病变(n = 4)、皮质侵蚀(n = 4)及矿化(n = 2)。磁共振成像(MRI)也显示病变信号强度不均匀且强化明显。骨闪烁显像显示单发性病变处放射性核素摄取呈偏心性增加(n = 10)。病理报告显示骨肉瘤(n = 7)、纤维肉瘤(n = 2)和恶性纤维组织细胞瘤(MFH)(n = 1)。研究结束时,1例患者死于肿瘤,1例患者存活但有肺转移,1例患者复发,7例患者存活且无复发。

有手术史的FD患者应进行随访,因为手术区域内的溶骨性病变强烈提示恶变。FD相关恶性肿瘤的影像学特征为边界不清、有矿化的溶骨性病变伴皮质破坏。需要进一步研究以探索FD恶变的发病机制并制定最佳治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f21/4602648/1e059ad5455e/medi-94-e369-g003.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验