单侧上肢远端Klippel-Trenaunay综合征及静脉缺乏1例报告。

JNMA; journal of the Nepal Medical Association Pub Date : 2025-02-01 Epub Date: 2025-02-28 DOI:10.31729/jnma.8892
Beenu Maharjan, Lian Liu, Xu Liu, Qingfeng Liu, Xian Jiang
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引用次数: 0

摘要

Klippel-Trenaunay综合征是一种罕见的先天性疾病,其特征是三种症状:毛细血管畸形、静脉异常、骨骼和软组织肥大。该综合征通常表现为葡萄酒色斑,静脉曲张和肢体肥大,可导致严重的并发症,如静脉血栓栓塞和出血。我们报告一例13岁的女性,出生后左上肢和肩部出现红斑。采用了一种有效的治疗方法,其中包括一个多学科的专家团队,专门从事皮肤病学和血管外科的各个领域,所有人都以患者的健康为核心进行合作。这种方法强调基于患者偏好的个性化策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Klippel-Trenaunay Syndrome in the Distal Part of the Unilateral Upper Limb and Venous Deficiency: A Case Report.

Klippel-Trenaunay Syndrome is a rare congenital disorder characterized by a triad of symptoms-capillary malformations, venous abnormalities, and hypertrophy of bones and soft tissues. The syndrome often presents with port wine stains, varicose veins, and limb hypertrophy, which can lead to significant complications such as venous thromboembolism and bleeding. We present a case of a 13 ' year female, with erythema in left upper limb and shoulder since birth.. An effective treatment method was employed, which incorporated a multidisciplinary team of experts specialized in various fields of dermatology and vascular surgery, all working collaboratively with the patient's well-being at the core of their efforts. This approach emphasized a personalized strategy based on the patient's preferences.

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