Goto Yukihiro, Sasajima Hiroyasu, Furuno Yuichi, Kawabe Takuya, Ohwada Kei, Yamanaka Takumi, Tatsuzawa Kazunori, Hashimoto Naoya
Department of Neurosurgery, Kyoto Prefectural University Graduate School of Medicine Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, Japan.
Department of Neurosurgery, Kyoto Prefectural University Graduate School of Medicine Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, Japan.
World Neurosurg. 2018 Nov;119:20-24. doi: 10.1016/j.wneu.2018.07.201. Epub 2018 Aug 1.
Intraosseous hemangioma is a rare bone tumor, accounting for 0.7%-1.0% of all bone tumors. It can occur at any age, but only 9% of cases are younger than 10 years old. Although this tumor is usually slow-growing and clinically silent, we experienced 2 pediatric patients undergoing surgery for skull hemangioma who presented with uncommon clinical manifestations.
Case 1 was a 9-year-old boy who presented with sudden onset of headache and was referred to our hospital. Radiologic images revealed an osteolytic oval lesion in the right parietal bone and acute subdural hemorrhage in the right cerebral hemisphere. The right parietal lesion was removed surgically. The lesion was found to have grown into the dura and to be adherent to the pia matter. The removed lesion was histologically confirmed to be a hemangioma. Case 2 was an 8-year-old girl who was referred to our hospital with an elastic mass that had been slowly enlarging for 7 years. Radiologic images revealed an osteolytic oval lesion in the right parietal bone. Surgical removal was thus planned. The lesion was found to be attached to the dura, and we removed the lesion with the surrounding bone and attached dura. Histologic examination confirmed the lesion to be a hemangioma.
Although skull hemangiomas show clinical heterogeneity, surgical removal is usually diagnostic and leads to good patient outcomes. On occasion, however, this tumor causes secondary changes in the dura, such that dural incision and dural plasty should be planned in advance of lesion removal.
骨内血管瘤是一种罕见的骨肿瘤,占所有骨肿瘤的0.7%-1.0%。它可发生于任何年龄,但仅9%的病例年龄小于10岁。尽管这种肿瘤通常生长缓慢且临床上无症状,但我们遇到2例接受颅骨血管瘤手术的儿科患者,他们表现出不常见的临床表现。
病例1是一名9岁男孩,突然出现头痛,被转诊至我院。影像学检查显示右侧顶骨有一个溶骨性椭圆形病变,右侧大脑半球有急性硬膜下出血。右侧顶骨病变经手术切除。发现病变已长入硬脑膜并与软脑膜粘连。切除的病变经组织学证实为血管瘤。病例2是一名8岁女孩,因一个弹性肿块缓慢增大7年被转诊至我院。影像学检查显示右侧顶骨有一个溶骨性椭圆形病变。因此计划进行手术切除。发现病变附着于硬脑膜,我们将病变连同周围骨质和附着的硬脑膜一并切除。组织学检查证实病变为血管瘤。
尽管颅骨血管瘤表现出临床异质性,但手术切除通常具有诊断意义,并能使患者获得良好的预后。然而,偶尔这种肿瘤会引起硬脑膜的继发性改变,因此在切除病变之前应提前计划硬膜切开和硬膜成形术。