Ferrozzi F, Zuccoli G, Bacchini E, Piazza P, Sigorini M, Virdis R
Istituto di Scienze Radiologiche, Università degli Studi, Parma.
Radiol Med. 1998 Dec;96(6):562-9.
To analyze the extracerebral manifestations of type 1 neurofibromatosis (NF-1), with special reference to peripheral nerve tumors.
The findings of 376 NF-1 patients (194 men and 182 women; age range: 0.1-48 years, mean: 8.1) were retrospectively reviewed. The patients had been submitted to abdominopelvic and superficial US and, in case of abnormal US findings or in the presence of symptoms, to CT and/or MRI. In addition, we considered 5 more patients (2 men and 3 women; age range: 50-72 years, mean: 64.4) with incomplete forms of NF-1 diagnosed after the finding of nerve sheath tumors. Biopsy (12 cases), surgery (10 cases), or clinical-instrumental follow-up were the study criteria.
In the first group of patients we identified 91 cutaneous, 222 subcutaneous, 11 pendulous and 25 internal neurofibromas. Plexiform neurofibromas were found in the neck (1 case), chest (6 cases), abdomen (16), pelvis (8). We also found 1 benign and 1 malignant Schwannomas, 2 nerve sheath fibrosarcomas, 1 dopamine-producing sympatoma and 1 spermacytoma. As for the second group of patients, we had 2 Schwannomas, 1 pulmonary neurofibroma, and 2 multiple plexiform neurofibromas. The neurofibromas exhibited homogeneous US hypoechogenicity or slight echogenicity, with little contrast enhancement at CT. MR showed peripheral hyperintensity and central hypointensity on T2-weighted sequences and marked contrast enhancement after gadolinium, sometimes with mostly central uptake. The plexiform neurofibromas, which are typical of NF-1, had poorly-defined or infiltrating margins, with similar findings to the previous ones but sometimes with less homogeneous patterns at both US and CT. The Schwannomas, which are a less common finding in NF-1, exhibited different features at MRI and CT, namely pseudo-liquid or solid-inhomogeneous patterns with irregular and inhomogeneous contrast enhancement relative to the Antoni A/B tumor component. In the malignant lesions we observed infiltrating patterns, with irregular and inhomogeneous contrast enhancement, arranged asymmetrically relative to the contralateral lesion.
Extra-axial neoplasms are a frequent finding in NF-1. Despite the extremely variable appearances of some lesions (particularly Schwannomas), the typical plexiform neurofibroma exhibits characteristic patterns. The diagnosis of malignancy often requires bioptic confirmation.
分析1型神经纤维瘤病(NF-1)的脑外表现,特别关注周围神经肿瘤。
回顾性分析376例NF-1患者(男194例,女182例;年龄范围:0.1 - 48岁,平均8.1岁)的检查结果。这些患者接受了腹部盆腔和浅表超声检查,若超声检查结果异常或有症状,则进一步接受CT和/或MRI检查。此外,我们还纳入了另外5例患者(男2例,女3例;年龄范围:50 - 72岁,平均64.4岁),他们在发现神经鞘瘤后被诊断为不完全型NF-1。研究标准为活检(12例)、手术(10例)或临床影像学随访。
在第一组患者中,我们发现了91个皮肤神经纤维瘤、222个皮下神经纤维瘤、11个悬垂性神经纤维瘤和25个内部神经纤维瘤。丛状神经纤维瘤见于颈部(1例)、胸部(6例)、腹部(16例)、骨盆(8例)。我们还发现了1例良性和1例恶性施万细胞瘤、2例神经鞘纤维肉瘤、1例产生多巴胺的交感神经瘤和1例精细胞瘤。对于第二组患者,我们发现了2例施万细胞瘤、1例肺神经纤维瘤和2例多发丛状神经纤维瘤。神经纤维瘤在超声检查中表现为均匀的低回声或轻度回声,CT增强扫描时强化不明显。磁共振成像(MR)在T2加权序列上显示外周高信号和中央低信号,钆剂增强后有明显强化,有时主要为中央摄取。典型的NF-1丛状神经纤维瘤边界不清或呈浸润性生长,超声和CT表现与上述相似,但有时不均匀性更明显。施万细胞瘤在NF-1中较少见,在MRI和CT上表现不同,即相对于Antoni A/B肿瘤成分,呈假液性或实性不均匀模式,对比增强不规则且不均匀。在恶性病变中,我们观察到浸润性模式,对比增强不规则且不均匀,相对于对侧病变不对称分布。
轴外肿瘤在NF-1中很常见。尽管一些病变(特别是施万细胞瘤)外观极为多样,但典型的丛状神经纤维瘤具有特征性表现。恶性肿瘤的诊断通常需要活检证实。