Torres-Mora Jorge, Ud Din Nasir, Ahrens William Albert, Folpe Andrew L
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester 55905, MN, USA.
Department of Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan.
Hum Pathol. 2016 Nov;57:22-27. doi: 10.1016/j.humpath.2016.06.017. Epub 2016 Jul 6.
Perineuriomas are rare peripheral nerve sheath tumors arising from or differentiating along the lines of normal perineurial cells. They can be divided into intraneural and soft tissue types, with the latter category including a significant number of morphological variants. Herein, we further expand their morphological spectrum to include "pseudolipoblastic" perineuriomas. These lesions occurred in the tongue of a 30-year-old man and in the triceps of a 67-year-old woman and were characterized by bland, epithelioid cells with striking intracytoplasmic vacuolization. The architecture varied, with some areas showing a striking "net-like" or "microreticular" pattern and smaller areas having a more typical spindled and whorled appearance. Clinical follow-up (5months and 52months, respectively) showed no evidence of local recurrence or metastasis. Multiple perineurial markers, including epithelial membrane antigen, claudin-1, GLUT-1, and collagen IV, were diffusely positive. Both cases were submitted in consultation out of concern that they represented high-grade liposarcomas. To the best of our knowledge, this unusual morphological variant of perineurioma has not been reported. These tumors appear to be entirely benign and should be cured with simple excision. Pseudolipoblastic perineuriomas should be distinguished from round cell and epithelioid pleomorphic liposarcomas, as well as from other tumors that may show prominent intracytoplasmic vacuolization.
神经束膜瘤是一种罕见的周围神经鞘瘤,起源于正常神经束膜细胞或沿其分化。它们可分为神经内型和软组织型,后者包括大量形态学变异型。在此,我们进一步扩展其形态学谱,将“假脂肪母细胞性”神经束膜瘤纳入其中。这些病变分别发生在一名30岁男性的舌部和一名67岁女性的三头肌,其特征为温和的上皮样细胞,胞质内有明显的空泡形成。结构多样,一些区域呈现出显著的“网状”或“微网状”模式,较小区域则具有更典型的梭形和漩涡状外观。临床随访(分别为5个月和52个月)未发现局部复发或转移的证据。多种神经束膜标记物,包括上皮膜抗原、claudin-1、葡萄糖转运蛋白1和IV型胶原,均呈弥漫性阳性。由于担心这两例代表高级别脂肪肉瘤,故提交会诊。据我们所知,这种不寻常的神经束膜瘤形态学变异型尚未见报道。这些肿瘤似乎完全良性,通过简单切除即可治愈。假脂肪母细胞性神经束膜瘤应与圆形细胞和上皮样多形性脂肪肉瘤以及其他可能显示显著胞质内空泡形成的肿瘤相鉴别。