双边的斯特格-韦伯综合征与软组织缩和三重大
Shivangi Singh1, Priyanka Kowe2, Gitesh U Sawatkar3
1Department of Dermatology, All India Institute of Medical Sciences - Nagpur, Nagpur, Maharashtra, India.
BMJ case reports
|May 21, 2025
概括
斯特格-韦伯综合征 (SWS) 是一种罕见的神经皮肤疾病. 这种病例突出了罕见的双边呈现的SWS与不寻常的软组织缩和三巨.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 皮肤病学 皮肤病学
背景情况:
- 斯特格-韦伯综合征 (SWS) 或脑三角管血管病,是一种罕见的先天性神经皮肤疾病.
- 它通常呈现出皮肤,眼睛和中枢神经系统发现的三位一体,通常包括单方面面部葡萄酒污点 (PWS).
- 双边PWS和相关异常很少被报告.
研究的目的:
- 报告一种罕见的双边斯特格-韦伯综合征病例.
- 在这个双边SWS表述中描述软组织缩和三重的相关发现.
主要方法:
- 病例报告,详细说明临床表现和诊断发现.
- 关于斯特格-韦伯综合征及其变体的相关文献的综述.
主要成果:
- 患者表现为双边面部葡萄酒污点,影响三角神经分支.
- 相关发现包括唇部软组织缩和三重壮成.
- 本次演讲扩大了已知的SWS表现的范围.
结论:
- 双边斯图尔奇-韦伯综合征可以呈现出独特和广泛的特征,超出了典型的三位一体.
- 早期识别非典型的SWS表现对于全面的患者管理至关重要.
- 需要进一步研究SWS的遗传和临床变异性.
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