Suppr超能文献

新生儿1型神经纤维瘤病合并贫血痣:1例报告

Nevus anemicus associated with neurofibromatosis type 1 in a neonate: a case report.

作者信息

Cerini C, Pogliani L, Mameli C, Zuccotti G V

机构信息

Department of Pediatrics, L. Sacco Hospital, University of Milan, Milan, Italy -

出版信息

G Ital Dermatol Venereol. 2015 Dec;150(6):745-7.

Abstract

Neurofibromatosis type 1 (NF1) is a multisystemic autosomal dominant disease affecting approximately 1 individual in 3500. The diagnostic criteria developed by NIH in 1988 allow unequivocal diagnosis in all cases but the youngest children. Due to the variable phenotypic expression, the diagnosis of NF1 in the youngest may be challenging, particularly when the distinctive cutaneous lesions are missing. We describe the case of a neonate who presented at birth solely with a nevus anemicus. Although this is not considered a diagnostic feature, given the presence of a few café au lait lesions in the patient's father, the genetic test was performed and the diagnosis of NF1 confirmed. To our knowledge, the association between nevus anemicus and NF1 is only anedoctal. The peculiarity clinical manifestation of this case highlights the high variable expressivity of the NF1 gene mutation and reinforces the importance of genetic counseling in affected individuals.

摘要

1型神经纤维瘤病(NF1)是一种多系统常染色体显性疾病,每3500人中约有1人患病。美国国立卫生研究院(NIH)1988年制定的诊断标准可明确诊断所有病例,但最年幼的儿童除外。由于表型表达的变异性,最年幼患者的NF1诊断可能具有挑战性,尤其是在缺少典型皮肤病变的情况下。我们描述了一名仅在出生时出现贫血痣的新生儿病例。虽然这并不被视为诊断特征,但鉴于患儿父亲有一些咖啡斑,因此进行了基因检测,确诊为NF1。据我们所知,贫血痣与NF1之间的关联仅有个案报道。该病例独特的临床表现突出了NF1基因突变的高变异性表达,并强化了对受影响个体进行遗传咨询的重要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验