Azura M, Vanel D, Alberghini M, Picci P, Staals E, Mercuri M
Musculoskeletal Oncological Surgery Department, Istituto Ortopedico Rizzoli, Via Pupilli 1, Bologna 40136, Italy.
Skeletal Radiol. 2009 Jul;38(7):685-90. doi: 10.1007/s00256-009-0672-3. Epub 2009 Mar 7.
This study was performed to assess the imaging findings in cases of parosteal osteosarcoma dedifferentiated into telangiectatic osteosarcoma. Parosteal osteosarcoma is a low-grade well-differentiated malignant tumor. Dedifferentiation into a more aggressive lesion is frequent and usually visible on imaging as a central lytic area in a sclerotic mass. Only one case of differentiation into a telangiectatic osteosarcoma has been reported. As it has practical consequences, with a need for aggressive chemotherapy, we looked for this rather typical imaging pattern.
Review of 199 cases of surface osteosarcomas (including 86 parosteal, of which 23 were dedifferentiated) revealed lesions suggesting a possible telangiectatic osteosarcoma on imaging examinations in five cases (cavities with fluid). Histology confirmed three cases (the two other only had hematoma inside a dedifferentiated tumor). There were three males, aged 24, 28, and 32. They had radiographs and CT, and two an MR examination.
Lesions involved the distal femur, proximal tibia, and proximal humerus. The parosteal osteosarcoma was a sclerotic, regular mass, attached to the cortex. A purely lytic mass, partially composed of fluid cavities was easily detected on CT and MR. It involved the medullary cavity twice, and remained outside the bone once. Histology confirmed the two components in each case. Two patients died of pulmonary metastases and one is alive.
Knowledge of this highly suggestive pattern should help guide the initial biopsy to diagnose the two components of the tumor, and guide aggressive treatment.
本研究旨在评估骨旁骨肉瘤去分化为毛细血管扩张型骨肉瘤病例的影像学表现。骨旁骨肉瘤是一种低级别、高分化的恶性肿瘤。去分化为更具侵袭性的病变很常见,在影像学上通常表现为硬化肿块内的中央溶骨区。仅报道过1例分化为毛细血管扩张型骨肉瘤的病例。由于其具有实际影响,需要积极的化疗,我们寻找这种相当典型的影像学表现。
回顾199例表面骨肉瘤病例(包括86例骨旁骨肉瘤,其中23例发生去分化),在影像学检查中发现5例病变提示可能为毛细血管扩张型骨肉瘤(有液性腔隙)。组织学证实3例(另外2例仅在去分化肿瘤内有血肿)。患者为3名男性,年龄分别为24岁、28岁和32岁。他们均进行了X线平片和CT检查,2例还进行了磁共振检查。
病变累及股骨远端、胫骨近端和肱骨近端。骨旁骨肉瘤为附着于皮质的硬化、规则肿块。在CT和磁共振上很容易检测到一个完全溶骨性肿块,部分由液性腔隙组成。它两次累及髓腔,一次位于骨外。组织学在每个病例中均证实了两种成分。2例患者死于肺转移,1例存活。
了解这种高度提示性的表现应有助于指导初始活检以诊断肿瘤的两种成分,并指导积极的治疗。