Mentzel T
Institut für Pathologie der Friedrich-Schiller-Universität Jena.
Pathologe. 1999 Mar;20(2):98-109. doi: 10.1007/s002920050327.
Until recently, benign cutaneous neural tumours which do not fulfil criteria for either neurofibrom or schwannoma often were lumped into the broad category of benign peripheral nerve sheath tumours (PNST). However, during the last years a number of new entities of neural tumours have been described, and advances in immunohistochemistry and electronmicroscopy have helped us to better understand the cytological differentiation in these neoplasms. The knowledge of these distinctive neoplasms is necessary in order to avoid diagnostic pitfalls and misdiagnosis of more aggressive neoplasms. These distinctive lesions include: neurothekeoma, which can divided into classical myxoid and cellular types showing characteristic histological and immunohistochemical features. Typical neurothekeoma (nerve sheath myxoma) is a lobular or nodular dermal neoplasm composed of plump spindled or stellated, S-100 positive tumour cells set in a maxoid stroma. In contrast, cellular neurothekeoma is characterized as an ill-defined dermal neoplasm composed of concentric nests and fascicles of spindle-shaped and epithelioid tumour cells, which are S-100 negative but stain positively for NKIC3. The evidence of intermediate forms of neurothekeoma showing features of ordinary hypocellular neurothekeoma and cellular neurothekeoma, as well as ultrastructural studies, emphasize that both variants represent a spectrum of neurothekeoma; solitary circumscribed neuroma ("palisaded encapsulated neuroma") manifests mainly as a skin-colored or pink papule or nodule, and is most often located on the face. Histologically, solitary circumscribed neuroma is a well-circumscribed round or ovoid dermal neoplasm composed of interwoven fascicles of schwann cells, which stain positively for S-100 protein and numerous neurofilament positive axons surrounded partly by fibroblasts and EMA-positive perineural cells; perineurioma is a rare well-circumscribed neoplasm which occurs mainly in subcutaneous tissue and only rarely in the dermis and in deep soft tissues. Perineurioma is composed of elongated bipolar spindle-shaped tumour cells which are arranged in storiform, whorled, linear or lamellated growth patterns, The tumour cells stain positively for vimentin and EMA, and for CD 34 in a number of cases, but lack positivity for S-100 protein, neurofilament and desmoplakin. In addition unusual forms of schwannoma (cellular schwannoma, solitary plexiform schwannoma, melanotic schwannoma) and neurofibroma ("atypical" (bizarre) neurofibroma, diffuse neurofibroma, epithelioid neurofibroma) are briefly discussed.
直到最近,不符合神经纤维瘤或神经鞘瘤标准的良性皮肤神经肿瘤通常被归为良性周围神经鞘瘤(PNST)这一宽泛类别。然而,在过去几年中,已描述了许多新的神经肿瘤实体,免疫组织化学和电子显微镜技术的进展帮助我们更好地理解这些肿瘤的细胞分化。了解这些独特的肿瘤对于避免诊断陷阱和更具侵袭性肿瘤的误诊是必要的。这些独特的病变包括:神经鞘黏液瘤,可分为经典黏液样型和细胞型,具有特征性的组织学和免疫组织化学特征。典型的神经鞘黏液瘤(神经鞘瘤黏液瘤)是一种小叶状或结节状真皮肿瘤,由丰满的梭形或星状、S-100阳性肿瘤细胞组成,位于黏液样基质中。相比之下,细胞性神经鞘黏液瘤的特征是一种边界不清的真皮肿瘤,由同心巢状和束状的梭形及上皮样肿瘤细胞组成,这些细胞S-100阴性,但对NKIC3呈阳性染色。显示普通少细胞性神经鞘黏液瘤和细胞性神经鞘黏液瘤特征的神经鞘黏液瘤中间型的证据以及超微结构研究强调,这两种变体代表了神经鞘黏液瘤的一个谱系;孤立性局限性神经瘤(“栅栏状包膜神经瘤”)主要表现为肤色或粉红色丘疹或结节,最常位于面部。组织学上,孤立性局限性神经瘤是一种边界清楚的圆形或椭圆形真皮肿瘤,由交织的神经鞘细胞束组成,对S-100蛋白呈阳性染色,并有许多神经丝阳性轴突,部分被成纤维细胞和EMA阳性的神经周细胞围绕;神经束膜瘤是一种罕见的边界清楚的肿瘤,主要发生于皮下组织,仅很少见于真皮和深部软组织。神经束膜瘤由细长的双极梭形肿瘤细胞组成,这些细胞呈漩涡状、轮状、线性或层状生长模式排列,肿瘤细胞对波形蛋白和EMA呈阳性染色,在一些病例中对CD 34呈阳性染色,但对S-100蛋白、神经丝和桥粒斑蛋白缺乏阳性反应。此外,还简要讨论了神经鞘瘤的不寻常形式(细胞性神经鞘瘤、孤立性丛状神经鞘瘤、黑色素性神经鞘瘤)和神经纤维瘤(“非典型”(怪异)神经纤维瘤、弥漫性神经纤维瘤、上皮样神经纤维瘤)。