Krastinova D, Kelly M B, Mihaylova M
Cranio-Orbito-Palpebral Surgery Unit, Hopital Foch, Suresnes, France.
Plast Reconstr Surg. 2001 Sep 15;108(4):817-26. doi: 10.1097/00006534-200109150-00001.
Congenital microphthalmos and anophthalmos are rare conditions in which orbital growth is deficient. Hypoplasia of the globe affects the bony orbit (micro-orbitism), the conjunctival sac, and eyelids (microblepharism), and it may be associated with abnormalities of the entire hemifacial skeleton (hemifacial microsomia). In the present article, the authors review a series of 19 patients with microphthalmos (nine had right-sided, one had bilateral, and nine had left-sided microphthalmos) who were treated in the Orbitopalpebral Unit at Hospital Foch over a period of 15 years (follow-up, 5 months to 18 years).Orbital expansion was achieved using spherical implants (n = 13), orbital osteotomies (n = 4), and orbital expanders (n = 2). Both expanders were removed within 6 months because of failure (one infection and one rupture). The current preferred method for orbital expansion is to use serial implants in the growing orbit and osteotomies in cases of late referral or insufficient orbital volume in the older child. The target proportions of the reconstructed orbit are not planned to mirror the healthy side exactly. The inferior orbital rim is kept higher to support the orbital implant, and the orbit is kept shallow to avoid a sunken appearance. Cranial bone grafts were used to augment deficient orbital contours; they were assisted by anterior transposition of the temporalis muscle (n = 5) when additional orbital volume was required. Conjunctival sac reconstruction was achieved by the use of serial conformers placed in the conjunctival sac during the neonatal period, followed by grafts of buccal mucosa and full-thickness skin maintained in place with a tarsorrhaphy for 3 to 6 months. Eyelid reconstruction using local flaps and skin grafts proved to be necessary in cases treated by osteotomy expansion, although reconstruction was not required after expansion using serial solid shapes. The results illustrate an evolution in approach and concepts of reconstruction of the microphthalmic orbit and emphasize the need for an integrated craniofacial approach for this complex deformity.
先天性小眼畸形和无眼畸形是眼眶发育不足的罕见病症。眼球发育不全影响骨性眼眶(小眼症)、结膜囊和眼睑(小睑症),并且可能与整个半侧面部骨骼异常(半侧颜面短小畸形)相关。在本文中,作者回顾了在富尔医院眼眶眼睑科接受治疗的19例小眼畸形患者(9例为右侧,1例为双侧,9例为左侧小眼畸形),治疗时间跨度为15年(随访时间为5个月至18年)。采用球形植入物(n = 13)、眼眶截骨术(n = 4)和眼眶扩张器(n = 2)实现眼眶扩张。由于失败(1例感染和1例破裂),两个扩张器均在6个月内取出。目前眼眶扩张的首选方法是在生长中的眼眶中使用系列植入物,对于大龄儿童晚期转诊或眼眶容积不足的情况则采用截骨术。重建眼眶的目标比例并非计划精确镜像健康侧。眶下缘保持较高以支撑眼眶植入物,眼眶保持较浅以避免凹陷外观。使用颅骨骨移植来增加不足的眼眶轮廓;当需要额外的眼眶容积时,通过颞肌前移位(n = 5)辅助。结膜囊重建通过在新生儿期在结膜囊中放置系列贴合器来实现,随后进行颊黏膜移植和全厚皮片移植,并用睑缘缝合术固定3至6个月。在采用截骨术扩张治疗的病例中,使用局部皮瓣和皮肤移植进行眼睑重建被证明是必要的,尽管在使用系列实心形状扩张后无需重建。结果说明了小眼畸形眼眶重建方法和概念的演变,并强调了针对这种复杂畸形采用综合颅面方法的必要性。