Yavuzer Reha, Tuncer Serhan, Başterzi Yavuz, Işik Ipek, Sari Alper, Latifoğlu Osman
Plastic, Reconstructive, and Aesthetic Surgery Department, Gazi University Faculty of Medicine, Ankara, Turkey.
Plast Reconstr Surg. 2004 Jan;113(1):34-44. doi: 10.1097/01.PRS.0000096704.34065.03.
The orbital floor is one of the most frequently damaged parts of the maxillofacial skeleton during facial trauma. Unfavorable aesthetic and functional outcomes are frequent when it is treated inadequately. The treatment consists of spanning the floor defect with a material that can provide structural support and restore the orbital volume. This material should also be biocompatible with the surrounding tissues and easily reshaped to fit the orbital floor. Although various autografts or synthetic materials have been used, there is still no consensus on the ideal reconstruction method of orbital floor defects. This study evaluated the applicability of solvent-preserved cadaveric cranial bone graft and its preliminary results in the reconstruction of the orbital floor fractures. Twenty-five orbital floor fractures of 21 patients who underwent surgical repair with cadaveric bone graft during a 2-year period were included in this study. Pure blowout fractures were determined in nine patients, whereas 12 patients had other accompanying maxillofacial fractures. Of the 21 patients, 14 had clinically evident diplopia (66.7 percent), 12 of them had enophthalmos (57.1 percent), and two of them had gaze restriction preoperatively. Reconstruction of the floor of the orbit was performed following either the subciliary or the transconjunctival approach. A cranial allograft was placed over the defect after sufficient exposure. The mean follow-up period was 9 months. Postoperative diplopia, enophthalmos, eye motility, cosmetic appearance, and complications were documented. None of the patients had any evidence of diplopia, limited eye movement, inflammatory reactions in soft tissues, infection, or graft extrusion in the postoperative period. Providing sufficient orbital volume, no graft resorption was detected in computed tomography scan controls. None of the implants required removal for any reason. Enophthalmos was seen in one patient, and temporary scleral show lasting up to 3 to 6 weeks was detected in another three patients. Satisfactory cosmetic results were obtained in all patients. This study showed that solvent-preserved bone, which is a nonsynthetic, human-originated, processed bioimplant, can be safely used in orbital floor repair and can be considered as another reliable treatment alternative.
眼眶底是面部创伤时颌面骨骼最常受损的部位之一。治疗不充分时,常出现不良的美学和功能结局。治疗方法包括用能提供结构支撑并恢复眼眶容积的材料覆盖眶底缺损。这种材料还应与周围组织生物相容,并易于塑形以适应眶底。尽管已使用了各种自体移植物或合成材料,但对于眶底缺损的理想重建方法仍未达成共识。本研究评估了溶剂保存的尸体颅骨移植的适用性及其在眶底骨折重建中的初步结果。本研究纳入了21例患者的25处眶底骨折,这些患者在2年期间接受了尸体骨移植手术修复。9例患者为单纯爆裂性骨折,12例患者伴有其他颌面骨折。21例患者中,14例有临床明显的复视(66.7%),其中12例有眼球内陷(57.1%),2例术前有凝视受限。采用睫毛下或经结膜入路进行眶底重建。充分暴露后,将同种异体颅骨移植片置于缺损处。平均随访期为9个月。记录术后复视、眼球内陷、眼球运动、外观及并发症情况。术后所有患者均无复视、眼球运动受限、软组织炎症反应、感染或移植片挤出的迹象。在计算机断层扫描对照中未检测到移植片吸收,提供了足够的眼眶容积,且无植入物因任何原因需要取出。1例患者出现眼球内陷,另3例患者出现持续3至6周的暂时性巩膜外露。所有患者均获得满意的外观效果。本研究表明,溶剂保存骨作为一种非合成的、源自人体的、经过处理的生物植入物,可安全用于眶底修复,可被视为另一种可靠的治疗选择。