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微血管游离皮瓣矫正严重半侧面部萎缩。

Microvascular free-flap correction of severe hemifacial atrophy.

作者信息

Longaker M T, Siebert J W

机构信息

Institute of Reconstructive Plastic Surgery, New York University Medical Center, N.Y., USA.

出版信息

Plast Reconstr Surg. 1995 Sep;96(4):800-9. doi: 10.1097/00006534-199509001-00006.

Abstract

Romberg's disease is a progressive hemifacial atrophy of unknown etiology. Microsurgical reconstruction, focusing on the correction of facial asymmetry and restoration of contour, has become the "gold standard." We report our experience with 15 patients involving 16 free-tissue transfers with a minimum of 1 year of follow-up who were treated from July of 1989 to January of 1993. All patients were classified as having severe atrophy. There were 7 males and 8 females in the series. Distribution of disease was a coup de sabre type or segmental pattern in 6 patients, whereas 9 patients had a hemifacial distribution. Fourteen patients had unilateral disease (7 right and 7 left), and 1 patient had bilateral atrophy. The average age of onset of disease was 11.9 years. The average duration of atrophy was 6.7 years. No patient was operated on with a quiescent interval of less than 2 years. Average age at operation was 28.7 years, with a range from 6 to 46 years. Follow-up ranged from 1 to 4.5 years. Two patients had facial hematomas as the only complication. No flaps were lost. Flap revisions consisting of minor contour corrections were performed in 10 patients. Limited recurrence of facial atrophy was seen in a single patient 2 years postoperatively. All patients rated their improvement as excellent. The deepithelialized extended parascapular flap with large fascial extensions of dorsal thoracic fascia is our procedure of choice. This fascia can be folded into variable thicknesses to correct subtle contour defects of the upper lip, medial canthus, eyelids, and ear that have reportedly been difficult to reconstruct.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

Romberg病是一种病因不明的进行性半侧面部萎缩。以纠正面部不对称和恢复轮廓为重点的显微外科重建已成为“金标准”。我们报告了1989年7月至1993年1月期间治疗的15例患者的经验,这些患者接受了16次游离组织移植,随访时间至少1年。所有患者均被归类为严重萎缩。该系列中有7名男性和8名女性。6例患者的疾病分布为剑击型或节段型,而9例患者为半侧面部分布。14例患者为单侧疾病(7例右侧和7例左侧),1例患者为双侧萎缩。疾病的平均发病年龄为11.9岁。萎缩的平均持续时间为6.7年。没有患者在静止期少于2年时接受手术。手术的平均年龄为28.7岁,范围为6至46岁。随访时间为1至4.5年。2例患者仅出现面部血肿这一并发症。没有皮瓣丢失。10例患者进行了包括轻微轮廓矫正的皮瓣修复。1例患者术后2年出现有限的面部萎缩复发。所有患者对改善情况的评价均为优秀。带有胸背筋膜大筋膜延伸的去上皮化扩大肩胛旁皮瓣是我们的首选术式。这种筋膜可以折叠成不同厚度,以纠正据报道难以重建的上唇、内眦、眼睑和耳部的细微轮廓缺陷。(摘要截短至250字)

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