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Microcystic pseudoglandular plexiform cutaneous neurofibroma

机译:微囊假腺丛状皮肤神经纤维瘤

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Glandular structures are well documented to appear in peripheral nerve sheath tumors. These epithelial elements are usually present in malignant peripheral nerve sheath tumors although a few cases of glandular benign peripheral nerve sheath tumors have also been described, most of them being schwannomas. A neurofibroma with glands is considered to be a rare type of divergent differentiation, but a neurofibroma containing gland-like or pseudoglandular structures have not, to our knowledge, been described. We report a 33-year-old patient with a well-demarcated dermal neoplasm, composed of neoplastic Schwann cells, perineurial-like cells and fibroblasts in a matrix with collagen fibers and myxoid areas. A part of the tumor consisted of microcystic gland-like spaces lined by flat cells. These cells were either S100 positive or negative, with no epithelial membrane antigen, cytokeratin or CD31 immunostaining. Recognition of the presence of pseudoglandular elements in neurofibromas is important to distinguish them from other tumoral lesions, some of them with malignant potential.
机译:已有文献证明腺体结构出现在周围神经鞘瘤中。这些上皮成分通常存在于恶性周围神经鞘瘤中,尽管也已经描述了少数腺体良性周围神经鞘瘤的病例,其中大多数是神经鞘瘤。具有腺体的神经纤维瘤被认为是罕见的分化分化类型,但是据我们所知,尚未描述含有腺样或假腺结构的神经纤维瘤。我们报告了一名33岁的患者,其皮肤肿瘤已明确划分,由肿瘤性雪旺氏细胞,会周神经样细胞和成纤维细胞组成,基质中含有胶原蛋白纤维和粘液状区域。肿瘤的一部分由扁平细胞内衬的微囊腺样空间组成。这些细胞是S100阳性或阴性,没有上皮膜抗原,细胞角蛋白或CD31免疫染色。认识到神经纤维瘤中存在假腺成分对于将它们与其他肿瘤病变区分开很重要,其中一些具有恶性潜能。

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