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整形手术在先天性皮肤松弛症中的作用:一项10年随访研究

The role of plastic surgery in congenital cutis laxa: a 10-year follow-up.

作者信息

Nahas F X, Sterman S, Gemperli R, Ferreira M C

机构信息

Plastic Surgery Division, Hospital Jaraguá, University of São Paulo School of Medicine, SP, Brazil.

出版信息

Plast Reconstr Surg. 1999 Sep;104(4):1174-8; discussion 1179.

PMID:10654761
Abstract

The clinical features and the plastic surgery management of a 23-year-old woman with cutis laxa are presented. Two rhytidectomies were performed in this patient within 1 year. The first was associated with a SMAS flap; the second employed a prehairline incision. The evolution of the aging facial appearance 10 years after the last face lift was evaluated and compared with the preoperative situation. Repeated face lifts seem to be an interesting way to manage patients with cutis laxa. Unlike patients with other disorders of the connective tissue, those with cutis laxa have no vascular fragility and heal well. The role of plastic surgery and the clinical features and timing for operation are reviewed and discussed.

摘要

本文介绍了一名23岁皮肤松弛症女性患者的临床特征及整形手术治疗情况。该患者在1年内接受了两次除皱手术。第一次手术联合了SMAS瓣;第二次手术采用了发际线前切口。评估并比较了最后一次面部提升术后10年面部老化外观的变化与术前情况。反复进行面部提升似乎是治疗皮肤松弛症患者的一种有效方法。与其他结缔组织疾病患者不同,皮肤松弛症患者没有血管脆性,愈合良好。本文对整形手术的作用、临床特征及手术时机进行了回顾和讨论。

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The role of plastic surgery in congenital cutis laxa: a 10-year follow-up.整形手术在先天性皮肤松弛症中的作用:一项10年随访研究
Plast Reconstr Surg. 1999 Sep;104(4):1174-8; discussion 1179.
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Generalized acquired cutis laxa treated with facial plastic surgery.采用面部整形手术治疗的全身性获得性皮肤松弛症。
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Bilateral congenital entropion with cutis laxa.双侧先天性睑内翻伴皮肤松弛症。
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Urol Case Rep. 2019 Sep 4;27:101011. doi: 10.1016/j.eucr.2019.101011. eCollection 2019 Nov.
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Acquired Localized Cutis Laxa: A Case Report and the Role of Plastic Surgery.获得性局限性皮肤松弛症:一例报告及整形手术的作用
Indian J Dermatol. 2019 Jan-Feb;64(1):55-58. doi: 10.4103/ijd.IJD_14_18.
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Matrix Biol. 2018 Oct;71-72:144-160. doi: 10.1016/j.matbio.2018.02.021. Epub 2018 Feb 28.
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New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations.常染色体显性遗传皮肤松弛症发病机制的新见解:报告 5 个 ELN 突变。
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