Galluzzi Paolo, De Francesco Sonia, Giacalone Giovanna, Cerase Alfonso, Monti Lucia, Vallone Ignazio Maria, Lazzeretti Luigi, Venturi Carlo, Hadjistilianou Theodora
Neuro-Imaging and Neuro-Interventional Unit, Azienda Ospedaliera e Universitaria Senese, Policlinico Santa Maria alle Scotte, Siena, Italy.
Eur J Ophthalmol. 2011 Sep-Oct;21(5):521-8. doi: 10.5301/EJO.2011.6298.
To assess the usefulness of magnetic resonance imaging (MRI) in assessing fibrovascularization progression into synthetic hydroxyapatite (HA) implants inserted in anophthalmic sockets of children submitted to enucleation.
We studied 23 HA orbital implants in 23 children who underwent enucleation for retinoblastoma. Each patient was examined by MRI within to 9 to 69 weeks after implant insertion (mean 34 weeks, median 30 weeks). No patient had received chemotherapy or radiotherapy at MRI examination. From each T1-weighted, fat-suppressed enhanced axial examination, the image depicting the center of the implant was identified. Enhancement was evaluated using a 5-point scale. Additionally, possible associated orbital and intracranial pathologies and implant migration or extrusion were evaluated.
All patients showed areas of enhancement of the implant consistent with the presence of fibrovascular ingrowth. There was no grade 1 enhancement in our series. Grade 2 was observed in 1 patient (4.34%), grade 3 in 7 patients (30.43%), grade 4 in 11 patients (47.82%), and grade 5 in 4 patients (17.39%). During follow-up there were no cases of clinically evident orbital infection, implant migration, or implant extrusion. No second tumor, optic nerve invasion, orbital extension, tumor relapse, or leptomeningeal brain seeding were noted.
In this series, enhanced MRI showed satisfactory fibrovascular ingrowth of orbital implants since the 13th week after HA spheres insertion, with a trend towards progressive enhancement during the following weeks. The data also confirm the advice to wait at least 5-6 months after enucleation to perform drilling and peg placement.
评估磁共振成像(MRI)在评估纤维血管化进程进入植入接受眼球摘除术儿童无眼球眼眶的合成羟基磷灰石(HA)植入物中的作用。
我们研究了23例因视网膜母细胞瘤接受眼球摘除术的儿童的23个HA眼眶植入物。每位患者在植入物插入后9至69周内接受MRI检查(平均34周,中位数30周)。在MRI检查时,没有患者接受过化疗或放疗。从每个T1加权、脂肪抑制增强轴向检查中,识别出描绘植入物中心的图像。使用5分制评估增强情况。此外,评估了可能相关的眼眶和颅内病变以及植入物迁移或挤出情况。
所有患者均显示植入物增强区域,与纤维血管长入一致。我们的系列中没有1级增强。1例患者(4.34%)观察到2级增强,7例患者(30.43%)观察到3级增强,11例患者(47.82%)观察到4级增强,4例患者(17.39%)观察到5级增强。在随访期间,没有临床明显的眼眶感染、植入物迁移或植入物挤出病例。未发现第二肿瘤、视神经侵犯、眼眶扩展、肿瘤复发或软脑膜播散。
在本系列中,增强MRI显示自HA球植入后第13周起眼眶植入物有令人满意的纤维血管长入,在接下来的几周内有逐渐增强的趋势。数据还证实了建议在眼球摘除术后至少等待5-6个月再进行钻孔和栓钉植入。