Surgical approach in a rare case of coloboma–choristoma

Andrea Spano , Elena Piozzi , Maurizio Cavallini , W. Franz Baruffaldi-Preis , Alessia Buscarini , Diego Foschi , Emilio Trabucchi
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引用次数: 6

Abstract

Embryogenic eyelid defects can be isolated or associated with malformative diseases, such as Tessier craniofacial clefts.

We describe the exceptional coexistence of upper eyelid coloboma and lower eyelid dermolipoma in a 45-day-old infant with a Tessier no. 0–1 cleft.

The surgical intervention carried out on this patient, which used a flap of subconjunctival choristoma and grafting of reshaped cutaneous and tarsal portions of a preauricular anlage, is presented as a technique for correcting congenital palpebral coloboma.

Adoption of this technique allowed virtually complete repair of the defect and gave an acceptable functional and cosmetic result.

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手术治疗罕见结肠瘤-脉络膜瘤1例
胚胎性眼睑缺陷可以是孤立的或与畸形疾病相关,如Tessier颅面裂。我们描述了一个特殊的共存的上眼睑缺损和下眼睑真皮脂肪瘤在45天出生的婴儿与Tessier no。0 - 1间隙。对该患者进行手术干预,使用结膜下膜瘤皮瓣和耳前基板的重塑皮肤和跗骨部分移植,作为纠正先天性眼睑结肠瘤的一种技术。采用这种技术几乎可以完全修复缺陷,并获得可接受的功能和美容结果。
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