Potepan P, Spagnoli I, Danesini G M, Laffranchi A, Gadda D, Mascheroni L, Guzzon A
Divisione Radiodiagnostica A, Istituto Nazionale Tumori, Milano.
Radiol Med. 1994 Jun;87(6):741-6.
The records of 3,795 cases of malignant melanoma treated at the INT (Milan) from 1975 to 1992 were reviewed. Histologic confirmation was obtained in all cases. Thirty-one patients (0.82%) with solitary or multiple skeletal metastases were identified. The review of conventional films, tomograms, CT, MR and bone scintigraphy images enabled us to detect 120 single bone lesions. The X-ray features were divided into two groups according to typical and atypical skeletal lesions. Typical bone metastases are osteolytic (87.5%), with medullary origin (91.6%), and they cannot be distinguished from other osteolytic metastases on the basis of imaging criteria alone. Lesion growth causes cortical erosion and destruction (46.6%), pathologic fractures (22.5%) and soft tissue involvement (12.5%). Lytic areas usually have ill-defined margins. Clear-cut outline is an uncommon finding. Atypical skeletal metastases exhibit a mixed osteolytic-osteoblastic pattern (10%), which is hardly ever completely osteoblastic (2.5%). Other unusual metastatic patterns include intense trabecular rarefaction with no detectable single lesion (3.3%), the presence of a well-defined sclerotic rim and periosteal reaction (12.5%). Atypical growth may cause extensive cortical destruction and periosteal production resembling osteogenic osteosarcoma. The various imaging methods show that conventional radiology has relatively poor sensitivity because of anatomical reasons, while MRI is the most sensitive method to detect skeletal localizations. Treatment changes the radiologic patterns of the lesions: recalcification, sclerotic rim, periosteal reaction are common response patterns. Finally, in spite of the above limitations, conventional radiology remains the method of choice to assess lesion evolution during the follow-up.
回顾了1975年至1992年在INT(米兰)接受治疗的3795例恶性黑色素瘤病例的记录。所有病例均获得组织学确诊。确定了31例(0.82%)有孤立性或多发性骨转移的患者。对传统X线片、体层摄影、CT、MR和骨闪烁显像图像的回顾使我们能够检测到120个单发性骨病变。根据典型和非典型骨病变,X线特征分为两组。典型骨转移为溶骨性(87.5%),起源于骨髓(91.6%),仅根据影像学标准无法将其与其他溶骨性转移区分开来。病变生长导致皮质侵蚀和破坏(46.6%)、病理性骨折(22.5%)和软组织受累(12.5%)。溶骨区边缘通常不清。轮廓清晰是不常见的表现。非典型骨转移表现为溶骨-成骨混合模式(10%),几乎从未完全成骨(2.5%)。其他不寻常的转移模式包括强烈的小梁稀疏但未检测到单个病变(3.3%)、存在清晰的硬化边缘和骨膜反应(12.5%)。非典型生长可能导致广泛的皮质破坏和类似成骨性骨肉瘤的骨膜反应。各种影像学方法表明,由于解剖学原因,传统放射学的敏感性相对较差,而MRI是检测骨转移的最敏感方法。治疗会改变病变的放射学模式:重新钙化、硬化边缘、骨膜反应是常见的反应模式。最后,尽管有上述局限性,传统放射学仍是随访期间评估病变进展的首选方法。