Krishnamurthy T, Niveditha S R
Kempegowda Institute of Medical Sciences, Department of Pathology, Bangalore. India.
Malays J Pathol. 2014 Dec;36(3):217-21.
Peripheral nerve sheath tumours (PNST) with epithelial appearing cells compromise a heterogeneous group of neoplasms that are rare and diagnostically challenging. Of these, malignant PNSTs with epithelioid features (epithelioid MPNST) are commonly described in literature. However benign epithelioid PNSTs are rare and till date about 38 cases have been described in the literature. We report a benign epithelioid PNST with light microscopical and immunohistochemical features suggestive of schwannoma, presenting as a thigh mass in a 23-year-old female. The tumour was encapsulated, showed epithelioid cells in aggregates, and expressed vimentin and S-100 positivity. There was no expression of CD34, CK, EMA, CD99, p63 and HMB 45. Typical Antoni A and Antoni B areas were absent. At 18 months follow-up, the patient was well.
具有上皮样细胞的周围神经鞘瘤(PNST)构成了一组异质性肿瘤,这些肿瘤罕见且诊断具有挑战性。其中,具有上皮样特征的恶性PNST(上皮样恶性周围神经鞘瘤)在文献中常有描述。然而,良性上皮样PNST很罕见,迄今为止文献中报道了约38例。我们报告了1例具有光镜和免疫组化特征提示为施万瘤的良性上皮样PNST,该肿瘤表现为一名23岁女性大腿部肿块。肿瘤有包膜,可见上皮样细胞聚集,波形蛋白和S-100呈阳性表达。CD34、细胞角蛋白(CK)、上皮膜抗原(EMA)、CD99、p63和HMB 45均无表达。无典型的Antoni A区和Antoni B区。随访18个月,患者情况良好。