1型神经纤维瘤病:一个儿科病例的临床和影像学观点。

Case Reports in Radiology Pub Date : 2025-06-03 eCollection Date: 2025-01-01 DOI:10.1155/crra/9912392
Puneet Kumar Choudhary, Ankit Kumar Meena, Arvinder Wander, Aakash Mahesan, Paramdeep Singh
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引用次数: 0

摘要

神经纤维瘤病(NF)是一种影响神经和皮肤的常见疾病。有两种主要类型:1型神经纤维瘤病(NF-1)(也称为von Recklinghausen病)和2型神经纤维瘤病(NF-2)(以前称为双侧声学NF或中枢NF)。NF-1约占病例的85%,在一般人群中患病率为1 / 5000。在30%-50%的NF-1病例中,没有家族史,这表明这些病例可能是由生殖细胞突变引起的,通常来自父亲。在这里,我们提出一个7岁男孩的皮肤和放射学特征NF-1。NF-1是最常见的神经皮肤综合征,需要长期监测相关并发症。在本病例中,我们旨在强调儿童NF-1的典型临床和放射学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurofibromatosis Type 1: Clinical and Imaging Perspectives From a Pediatric Case.

Neurofibromatosis (NF) is a common disorder that affects the nerves and skin. There are two main types: neurofibromatosis Type 1 (NF-1) (also called von Recklinghausen's disease) and neurofibromatosis Type 2 (NF-2) (previously known as bilateral acoustic NF or central NF). NF-1 makes up approximately 85% of cases, with a prevalence of 1 in 5000 in the general population. In 30%-50% of NF-1 cases, there is no family history, suggesting that these cases likely result from germ cell mutations, often from the father. Here, we present the case of a 7-year-old boy with skin and radiological features of NF-1. NF-1 is the most common neurocutaneous syndrome, requiring long-term monitoring for related complications. In this case, we aimed to highlight the typical clinical and radiological features of NF-1 in a child.

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