Losee Joseph E, Afifi Ahmed, Jiang Shao, Smith Darren, Chao Mimi T, Vecchione Lisa, Hertle Richard, Davis John, Naran Sanjay, Hughes Jane, Paviglianiti Joseph, Deleyiannis Frederic W-B
Pittsburgh, Pa. From the Children's Hospital of Pittsburgh.
Plast Reconstr Surg. 2008 Sep;122(3):886-897. doi: 10.1097/PRS.0b013e3181811e48.
Scarce literature exists addressing the presentation, classification, and management of pediatric orbital fractures. The aim of this study is to review the authors' experience with the presentation, management, and early follow-up of pediatric orbital fractures.
A retrospective review of pediatric orbital fractures presenting to the Children's Hospital of Pittsburgh between 2003 and 2007 was performed. Demographics, associated injuries, computed tomographic scan findings, management, and follow-up were collected. From these data, a pediatric orbital fracture classification system was devised.
Seventy-four patients (81 orbits) were reviewed. Average age at presentation was 8.6 years. Fractures were distributed as follows: type 1, 40.7 percent; type 2, 33 percent; and type 3, 25.9 percent. Twenty-three orbits were treated surgically and 58 were treated nonoperatively. The operative rates were as follows: type 1, 9.1 percent; type 2, 14.8 percent; and type 3, 76.2 percent. Complications included minor enophthalmos in seven patients, and persistent cerebrospinal fluid leak in two growing skull fractures. For type 1 (pure orbital) fractures, three (12 percent) underwent surgical treatment for acute enophthalmos, vertical orbital dystopia, or muscle entrapment. Twenty-two orbits (88 percent) were managed nonoperatively. At an average follow-up of 13 months, minimal enophthalmos (1 to 2 mm) was found in one of the surgically treated fractures (33 percent) and in three of the conservatively managed fractures (13.6 percent).
For type 1 (pure orbital) fractures, unless there is evidence of acute enophthalmos, vertical orbital dystopia, or muscle entrapment, a nonoperative approach is advocated. Type 2 (craniofacial) fractures should be followed with serial computed tomographic scans; and type 3 (common fracture patterns) fractures have a greater chance of requiring surgery.
关于小儿眼眶骨折的表现、分类及处理的文献较少。本研究旨在回顾作者在小儿眼眶骨折的表现、处理及早期随访方面的经验。
对2003年至2007年在匹兹堡儿童医院就诊的小儿眼眶骨折进行回顾性研究。收集人口统计学资料、相关损伤、计算机断层扫描结果、处理方式及随访情况。基于这些数据,设计了一种小儿眼眶骨折分类系统。
共回顾了74例患者(81个眼眶)。就诊时的平均年龄为8.6岁。骨折分布如下:1型占40.7%;2型占33%;3型占25.9%。23个眼眶接受了手术治疗,58个眼眶接受了非手术治疗。手术率如下:1型为9.1%;2型为14.8%;3型为76.2%。并发症包括7例患者出现轻度眼球内陷,2例生长性颅骨骨折出现持续性脑脊液漏。对于1型(单纯眼眶)骨折,3例(12%)因急性眼球内陷、垂直性眼眶移位或肌肉嵌顿接受了手术治疗。22个眼眶(88%)接受了非手术治疗。平均随访13个月时,手术治疗的骨折中有1例(33%)出现轻度眼球内陷(1至2毫米),保守治疗的骨折中有3例(13.6%)出现轻度眼球内陷。
对于1型(单纯眼眶)骨折,除非有急性眼球内陷、垂直性眼眶移位或肌肉嵌顿的证据,否则提倡非手术治疗。2型(颅面)骨折应通过系列计算机断层扫描进行随访;3型(常见骨折类型)骨折更有可能需要手术治疗。