5岁男孩的Klippel Trenaunay综合征:罕见的胚胎血管异常

Heena Singdia
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引用次数: 0

摘要

我们报告一个5岁男孩的病例史,非近亲婚姻出生,顺利阴道分娩,以四肢长度差异,右腿的长度和周长大于左腿,右腹股沟区域静脉扩张,右半边身体有4年的葡萄酒色斑,病情随着孩子年龄的增长而发展。无溃疡史、雷诺现象、感觉异常、行走困难或足部水肿。基线检查、彩色多普勒和下肢x线检查正常。Klippel血管畸形综合征是一种由葡萄酒染色、肢体肥厚和静脉曲张组成的血管畸形疾病,全球发病率为5例/100000。
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 a 5 Year Old Boy: A Rare Embryological Vascular Anomaly
We present a case history of 5 years old boy, born of a non-consanguineous marriage with uneventful vaginal delivery brought to OPD with complaints of limb length discrepancy where the length and girth of right leg was greater than the left leg, dilated veins over right inguinal area and port wine stain over right half of the body for 4 years, the condition progresses with progressing age of child. There was no history of ulceration, Raynauds phenomenon, paresthesia, difficulty in walking or pedal edema. Baseline investigations, Color Doppler, and X-ray lower limb were normal. Klippel trenaunay syndrome is a vascular malformation disorder comprising a triad of port wine stain, limb hypertrophy and varicosities with a global incidence of 5 cases/100000.
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