Boumdin H, el Quessar A, Chakir N, el Hassani M R, Jiddane M
Service de Neuroradiologie, Hôpital des Spécialités ONO, Rabat, Maroc.
J Neuroradiol. 2001 Sep;28(3):200-4.
Primary Ewing sarcoma of the calvarial skull is very rare, found in less than 1% of the cases. Frontal and parietal convexities are the common sites of occurrence. We report two cases of primary Ewing sarcoma of the skull (in 13- and 14-year-old boys. The first tumor involved the right temporal region and exhibited unclear osteolytic appearance on skull x-rays while computed tomography showed an extraaxial enhanced mass and bone sclerosis with spiculated periosteal reaction. In the second case, the tumor was temporoparietal. Plain films demonstrated a large osteolysis and computed tomography revealed extensive bone destruction involving both the inner and outer tables. In both cases, the C scan revealed extraaxial enhanced masses with intracranial and extracranial extension. Radial resection was performed. Adjuvant chemotherapy was given and no recurrence or metastasis has occurred two years later.
颅骨原发性尤因肉瘤非常罕见,在不到1%的病例中被发现。额部和顶叶凸面是常见的发病部位。我们报告两例颅骨原发性尤因肉瘤病例(分别为13岁和14岁男孩)。第一例肿瘤累及右侧颞区,颅骨X线片显示溶骨性表现不清晰,而计算机断层扫描显示轴外强化肿块及骨硬化伴针状骨膜反应。第二例肿瘤位于颞顶部。平片显示大片骨质溶解,计算机断层扫描显示内外板均有广泛骨质破坏。两例病例的计算机断层扫描均显示轴外强化肿块并向颅内和颅外扩展。均进行了根治性切除。给予辅助化疗,两年后未出现复发或转移。