Republication de : Stimulator of interferon genes-associated vasculopathy with onset in infancy (SAVI syndrome): A case report

Q4 Medicine
M. Saro-Buendía , M. Mansilla-Polo , A. García-Piñero , M. Armengot-Carceller
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引用次数: 0

Abstract

Introduction

To document through a case report the ENT manifestations of the STING-associated vasculopathy with onset in infancy (SAVI) syndrome, remarking their value to achieve the diagnosis.

Case summary

A man in his forties presented with exercise-related dyspnoea and cold-exacerbated painful lesions over the nasal tip, cheeks, ears, and feet since his early childhood. The ENT manifestations included cartilaginous necrosis (both auricles and nasal tip) and a 1-cm anterior septal perforation. A familiar inheritance pattern was evident and genetic studies confirmed the diagnosis of a SAVI syndrome. Therapy with JAK inhibitors was implemented, resulting in a favorable response.

Discussion

SAVI syndrome is a recently described disease with recognizable otolaryngologic manifestations that may be key to clinical suspicion and genetic diagnosis.
干扰素基因相关的婴儿期血管病变(SAVI综合征):1例报告
通过病例报告记录婴儿期起病的sting相关血管病变(SAVI)综合征的耳鼻喉科表现,并指出其对实现诊断的价值。病例总结:男性,40多岁,自幼出现运动相关的呼吸困难和鼻尖、脸颊、耳朵和足部的寒冷加重的疼痛病变。耳鼻喉部表现为软骨坏死(耳廓和鼻尖)和1厘米前鼻中隔穿孔。一个熟悉的遗传模式是明显的,遗传研究证实了SAVI综合征的诊断。采用JAK抑制剂治疗,产生良好的反应。savi综合征是一种新近发现的疾病,具有可识别的耳鼻喉科表现,这可能是临床怀疑和遗传诊断的关键。
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来源期刊
CiteScore
0.10
自引率
0.00%
发文量
93
审稿时长
51 days
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