Rank J P, Rostad S W
University of Washington Medical Center, Seattle, USA.
Arch Pathol Lab Med. 1998 Apr;122(4):366-70.
We present the case of a peripheral nerve sheath tumor arising from the sciatic nerve in the thigh of a 42-year-old woman. Histologically, the tumor was composed of fascicles of spindle cells with extremely attenuated cytoplasmic processes. Regions of the tumor were heavily mineralized and fibrotic. The tumor was epithelial membrane antigen-positive and S100-negative. Staining for Leu-7 was positive in a patchy distribution. Type IV collagen was present between cells, and CD34 was negative in the tumor cells. Ultrastructural features included elongate cellular processes surrounded by discontinuous basal lamina and collagen. The features of the tumor therefore meet criteria for perineurioma. This rare tumor is found most often in the extremities in middle-aged woman. To our knowledge, the presence of bone formation in a perineurioma has not been described previously. The differential diagnosis includes other peripheral nerve sheath tumors, low-grade fibrous tumors, and synovial (monophasic) tumors. Evidence provided by electron microscopy and immunohistochemistry supports the diagnosis and classification of this unusual nerve sheath tumor as perineurioma with ossification. These findings expand our knowledge and criteria for classifying peripheral nerve sheath tumors.
我们报告一例发生于一名42岁女性大腿坐骨神经的周围神经鞘瘤病例。组织学上,肿瘤由梭形细胞束组成,胞质突起极细。肿瘤区域有大量矿化和纤维化。肿瘤上皮膜抗原阳性,S100阴性。Leu-7染色呈斑片状阳性。IV型胶原存在于细胞之间,肿瘤细胞CD34阴性。超微结构特征包括被不连续基底膜和胶原包围的细长细胞突起。因此,该肿瘤的特征符合神经束膜瘤的标准。这种罕见肿瘤最常见于中年女性的四肢。据我们所知,神经束膜瘤中骨形成的情况此前尚未见报道。鉴别诊断包括其他周围神经鞘瘤、低级别纤维瘤和滑膜(单相)肿瘤。电子显微镜和免疫组织化学提供的证据支持将这种不寻常的神经鞘瘤诊断和分类为伴有骨化的神经束膜瘤。这些发现扩展了我们对周围神经鞘瘤分类的认识和标准。