Posnick J C, Goldstein J A, Armstrong D, Rutka J T
Division of Plastic Surgery, Georgetown University Medical Center, Washington, D.C.
Neurosurgery. 1993 May;32(5):785-91; discussion 791. doi: 10.1227/00006123-199305000-00011.
This article presents the long-term results of skull defect reconstruction in a series of 27 children studied between 1986 and 1990 (mean age, 8.4 yr; range, 1-17 yr). Causes of their defects were encephalocele (six patients), trauma (seven patients), tumor (eight patients), fibrous dysplasia (two patients), postsynostectomy defects (two patients), osteomyelitis (one patient), and Reye's syndrome with bone flap loss (one patient). All patients underwent clinical and computed tomographic scan documentation of their skull defects before and immediately after surgery and at least 1 year later. The average preoperative defect surface area measured 33 cm2 (range, 2.5-114 cm2). Skull defects were reconstructed in all patients with fixed autogenous cranial bone grafts. In the initial five patients, the grafts were fixed with interosseous wires, and in the remainder, they were fixed with a combination of miniplates and microplates and screws. Follow-up ranged from 12 to 66 months (mean, 31.4 mo). Complications were minimal, with no infection, plate or graft exposure, or intracranial injuries. In 24 of 27 patients, clinical examination and computed tomographic scans showed no evidence of skull defect or appreciable irregularity of donor or recipient sites. Two patients had documented small regions of graft resorption. One skull had palpable contour irregularities but without a bony defect. All patients have resumed routine activities and sports without special head protection. Repair of skull defects in children with fixed autogenous cranial grafts is a reliable method of reconstruction with minimal morbidity. Although we prefer miniplates and microplates and screws for fixation, the grafts fixed in place with interosseous wires did equally well.
本文介绍了1986年至1990年间对27例儿童颅骨缺损修复的长期结果(平均年龄8.4岁;范围1 - 17岁)。其缺损原因包括脑膨出(6例)、外伤(7例)、肿瘤(8例)、骨纤维异常增殖症(2例)、颅骨切开术后缺损(2例)、骨髓炎(1例)以及伴有骨瓣丢失的瑞氏综合征(1例)。所有患者在手术前后及术后至少1年均接受了颅骨缺损的临床及计算机断层扫描记录。术前缺损平均表面积为33平方厘米(范围2.5 - 114平方厘米)。所有患者均采用自体颅骨固定移植片修复颅骨缺损。最初的5例患者采用骨间钢丝固定移植片,其余患者则采用微型钢板、微型钛板及螺钉联合固定。随访时间为12至66个月(平均31.4个月)。并发症极少,无感染、钢板或移植片外露或颅内损伤。27例患者中有24例临床检查及计算机断层扫描显示无颅骨缺损迹象,供区或受区无明显不规则。2例患者记录有小面积移植片吸收。1例颅骨可触及轮廓不规则但无骨缺损。所有患者均已恢复日常活动及运动,无需特殊头部保护。采用自体颅骨固定移植片修复儿童颅骨缺损是一种可靠的重建方法,发病率极低。虽然我们更倾向于使用微型钢板、微型钛板及螺钉进行固定,但采用骨间钢丝固定的移植片效果同样良好。