带蒂前臂桡侧皮瓣治疗Werner综合征双侧肘部溃疡1例的长期随访。

IF 0.4 Q4 SURGERY
Case Reports in Plastic Surgery and Hand Surgery Pub Date : 2025-02-08 eCollection Date: 2025-01-01 DOI:10.1080/23320885.2025.2463321
Yusuke Hayashibara, Kenji Kawamura, Hideo Hasegawa, Shohei Omokawa, Yasuhito Tanaka
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引用次数: 0

摘要

Werner综合征是一种罕见的常染色体隐性遗传病,由WRN基因突变引起,导致过早衰老和基因组不稳定。临床症状包括糖尿病、皮肤病变和微血管问题,患者经常在小腿远端、足部和肘部出现难以愈合的溃疡。手术治疗,如皮瓣手术,很少报道。我们提出的情况下,45岁的男性与维尔纳综合征谁发展难治性溃疡双肘。尽管保守治疗,溃疡持续存在,导致桡骨前臂蒂皮瓣手术成功。术后结果良好,16年随访期间无并发症、溃疡复发或感染。患者双肘活动范围保持完整。本病例强调了在Werner综合征中管理溃疡的挑战和皮瓣手术的成功长期结果,为这种罕见疾病的治疗提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term follow-up of a case of bilateral elbow ulcers in a patient with Werner syndrome treated with pedicled radial forearm flaps.

Werner syndrome is a rare autosomal recessive disorder caused by WRN gene mutations, leading to premature aging and genomic instability. Clinical symptoms include diabetes, skin lesions, and microvascular issues, with patients frequently developing difficult-to-heal ulcers on the distal legs, feet, and elbows. Surgical treatments, such as flap surgery, are rarely reported. We present the case of a 45-year-old male with Werner syndrome who developed refractory ulcers on both elbows. Despite conservative treatments, the ulcers persisted, leading to successful radial forearm pedicle flap surgeries. Postoperative results were favorable, with no complications, ulcer recurrence, or infections over a 16-year follow-up period. The patient maintained a full range of motion in both elbows. This case highlights the challenges of managing ulcers in Werner syndrome and the successful long-term outcomes of flap surgery, providing valuable insights into this rare condition's treatment.

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