Exploring the Complexity of Klippel-Trenaunay Syndrome: A Case Study and Review.

Shivam Tyagi, J K Giriraj Harshavardhan
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引用次数: 0

Abstract

Introduction: Klippel-Trenaunay syndrome (KTS) is a rare congenital condition characterized by the classical triad of port-wine stains, varicosities, and hypertrophy of bone and soft tissue.

Case report: A 5-year-old boy presented with swelling and varicose plaques on his right ankle with normal spine findings. He was diagnosed with KTS after relevant radiological investigations. Typically, management involves conservative measures such as compression stockings to alleviate edema due to chronic venous insufficiency, modern pneumatic compression devices, and occasionally surgical correction of varicose veins with lifelong monitoring.

Conclusion: This case report offers a concise overview of the clinical and pathological features of KTS, as well as its management strategies.

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探讨Klippel-Trenaunay综合征的复杂性:个案研究与回顾。
简介:klipppel - trenaunay综合征(KTS)是一种罕见的先天性疾病,其特征是典型的葡萄酒色斑,静脉曲张,骨和软组织肥大。病例报告:一名5岁男孩表现为右脚踝肿胀和静脉曲张斑块,脊柱表现正常。经相关放射检查后,他被诊断为KTS。通常情况下,治疗包括保守措施,如压缩长袜以减轻慢性静脉功能不全引起的水肿,现代气动压缩装置,偶尔手术矫正静脉曲张并终生监测。结论:本病例报告简要概述了KTS的临床和病理特征,以及治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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