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下肢纤维脂肪血管异常——病例报告

Lower Extremity Fibro-Adipose Vascular Anomaly-Case Report.

作者信息

Ferreira Joana, López Gutiérrez Juan Carlos, Carneiro Alexandre, Sousa Pedro Pinto, Braga Sandrina, Simões João Correia, Carrilho Celso, Mesquita Amílcar

机构信息

Life and Health Science Research Institute (ICVS), School of Health Science, University of Minho, Serviço de Cirurgia Vascular e Centro Académico do Hospital da Senhora da Oliveira Guimarães, Portugal.

Vascular Anomalies Center, Department of Pediatric Surgery, La Paz Children's Hospital, Madrid, Spain.

出版信息

Ann Vasc Surg. 2020 Jul;66:671.e15-671.e18. doi: 10.1016/j.avsg.2020.01.089. Epub 2020 Feb 1.

Abstract

Fibro-adipose vascular anomaly (FAVA) is a painful complex vascular malformation, characterized by muscle fibrofatty infiltration, usually in lower limb, associated with contracture of the ipsilateral extremity. This article describes the first case of FAVA reported in Portugal successfully treated with surgery. A 9-year-old female was admitted complaining of a painful mass in the right leg. The MRI scan showed the presence of a 5 × 4 × 4 cm mass in the right leg consistent with FAVA located in the peroneus longus muscle. The patient underwent resection of the involved muscle. She had 6 months of follow-up without any relevant clinical event. The authors also highlight the difference between FAVA and venous malformation. Early surgery is a treatment option that can prevent long-term consequences, as contracture and movement limitation.

摘要

纤维脂肪性血管异常(FAVA)是一种疼痛性复杂血管畸形,其特征为肌肉纤维脂肪浸润,通常发生于下肢,并伴有同侧肢体挛缩。本文描述了葡萄牙报道的首例经手术成功治疗的FAVA病例。一名9岁女性因右腿疼痛性肿块入院。磁共振成像(MRI)扫描显示右腿有一个5×4×4厘米的肿块,符合位于腓骨长肌的FAVA。患者接受了受累肌肉切除术。她接受了6个月的随访,没有发生任何相关临床事件。作者还强调了FAVA与静脉畸形之间的差异。早期手术是一种可以预防诸如挛缩和运动受限等长期后果的治疗选择。

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