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[孤立性结节状丛状神经纤维瘤。1型神经纤维瘤病的一个罕见病例]

[Exclusive nodular plexiform neurofibroma. An unusual case of neurofibromatosis type 1].

作者信息

Benchikhi H, Zeller J, Wolkenstein P, Wechsler J, Vidaud D, Revuz J

机构信息

Service de Dermatologie, Hôpital Henri-Mondor, Créteil.

出版信息

Ann Dermatol Venereol. 1995;122(9):601-3.

PMID:8745684
Abstract

INTRODUCTION

Type 1 neurofibromatous tumours (NF) are benign skin tumours which include cutaneous, subcutaneous and plexiform neurofibromas. Plexiform neurofibromas are either diffuse or nodular, the latter form being much more frequent.

CASE REPORT

We observed a particular form of neurofibroma in an 18-year-old patient who developed large deep subcutaneous which histology examination revealed to be exclusively nodular plexiform neurofibromas. The patient also had 6 café au lait spots leading to the diagnosis of sporadic NF 1. He did not have acoustic neuronoma, schwannoma or posterior cataract, eliminating NF 2.

COMMENTS

In NF 1, subcutaneous neurofibromas develop in 5 p. 100 of the patients. These lesions are termed nodular plexiform neurofibromas when they form long formations along nerve branches. The exclusive nature of the nodular plexiform neurofibromas in our case was exceptional. It could be hypothesized that the particular phenotype in our patient might correspond to a particular anomaly of the NF 1 gene.

摘要

引言

1型神经纤维瘤(NF)是良性皮肤肿瘤,包括皮肤、皮下和丛状神经纤维瘤。丛状神经纤维瘤可为弥漫性或结节性,后一种形式更为常见。

病例报告

我们在一名18岁患者中观察到一种特殊形式的神经纤维瘤,该患者出现了大的深部皮下肿物,组织学检查显示完全为结节性丛状神经纤维瘤。该患者还有6个咖啡斑,从而诊断为散发性NF 1。他没有听神经瘤、神经鞘瘤或后发性白内障,排除了NF 2。

评论

在NF 1中,5%的患者会出现皮下神经纤维瘤。当这些病变沿神经分支形成长条状结构时,被称为结节性丛状神经纤维瘤。我们病例中结节性丛状神经纤维瘤的单一性是罕见的。可以推测,我们患者的特殊表型可能对应于NF 1基因的特定异常。

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