Yamashita Kyoko, Funauchi Yuki, Hayakawa Keiko, Ae Keisuke, Matsumoto Seiichi, Ikuta Kunihiro, Nishida Yoshihiro, Ueno Teruko, Shimoyama Yoshie, Hiruta Nobuyuki, Machinami Rikuo, Kawachi Hiroshi, Takeuchi Kengo
Department of Pathology, the Cancer Institute Hospital, Japanese Foundation for Cancer Research, 3-8-31, Ariake, Koto, Tokyo, 135-8550, Japan.
Division of Pathology, the Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Virchows Arch. 2022 Jun;480(6):1269-1275. doi: 10.1007/s00428-021-03218-y. Epub 2021 Oct 12.
Epithelioid malignant peripheral nerve sheath tumor (MPNST) is a rare subtype of MPNST composed of epithelioid cells with abundant cytoplasm. Currently, strong and diffuse immunostaining for S100 protein and SOX10 is generally regarded as a characteristic feature of epithelioid MPNST. However, malignant tumors with epithelioid morphology that arise from a peripheral nerve or a pre-existing benign nerve sheath tumor should be regarded as epithelioid MPNSTs when they do not show characteristic features that definitively lead to other specific diagnoses. Here, we describe 3 cases of epithelioid MPNST in the peripheral nerve or schwannoma that was negative for S100 protein and SOX10 expression. Instead, these tumors were positive for EMA, GLUT1, claudin 1, and cytokeratin to varying degrees, while all of them retained SMARCB1 and H3K27me3 by immunohistochemistry. EMA, GLUT1, and claudin 1 are known markers of perineurial cell differentiation; thus, they could possibly represent epithelioid MPNST with perineurial cell differentiation.
上皮样恶性外周神经鞘瘤(MPNST)是MPNST的一种罕见亚型,由具有丰富细胞质的上皮样细胞组成。目前,S100蛋白和SOX10的强而弥漫性免疫染色通常被视为上皮样MPNST的特征性表现。然而,起源于外周神经或先前存在的良性神经鞘瘤的具有上皮样形态的恶性肿瘤,若未表现出明确指向其他特定诊断的特征性表现,则应被视为上皮样MPNST。在此,我们描述了3例发生于外周神经或施万瘤的上皮样MPNST,其S100蛋白和SOX10表达均为阴性。相反,这些肿瘤不同程度地表达EMA、GLUT1、claudin 1和细胞角蛋白,而通过免疫组化检测它们均保留了SMARCB1和H3K27me3。EMA、GLUT1和claudin 1是已知的神经束膜细胞分化标志物;因此,它们可能代表具有神经束膜细胞分化的上皮样MPNST。