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1型神经纤维瘤病患者的心脏神经纤维瘤罕见病例:影像学表现

A Rare Case of Cardiac Neurofibroma in a Patient with Neurofibromatosis Type 1: Radiologic Findings.

作者信息

Seo Sanghyun, Rho Ji Young

出版信息

Taehan Yongsang Uihakhoe Chi. 2021 Sep;82(5):1321-1327. doi: 10.3348/jksr.2020.0168. Epub 2021 Jun 16.

Abstract

Neurofibromatosis type 1 (NF1) is a relatively common inherited disorder characterized by the formation of neurofibromas, pigmentary abnormalities of the skin, Lisch nodules of the iris, and skeletal abnormalities. Multiple cutaneous neurofibromas are benign nerve sheath tumors and the main manifestation of NF1. Cardiac neurofibroma associated with NF1 is very rare, and few cases have been reported in the literature. Herein, we present the CT and MRI findings of a surgically confirmed left ventricular neurofibroma in a 32-year-old female with NF1.

摘要

1型神经纤维瘤病(NF1)是一种相对常见的遗传性疾病,其特征为神经纤维瘤的形成、皮肤色素异常、虹膜错构瘤和骨骼异常。多发性皮肤神经纤维瘤是良性神经鞘瘤,也是NF1的主要表现。与NF1相关的心脏神经纤维瘤非常罕见,文献中报道的病例很少。在此,我们展示了一名32岁患有NF1的女性经手术证实的左心室神经纤维瘤的CT和MRI表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/938c/9432373/250a6b6c5046/jksr-82-1321-g001.jpg

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