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唾液腺黏液表皮样肿瘤的超微结构及临床病理特征(作者译)

[Ultrastructure and clinicopathological aspects of mucoepidermoid tumour of the salivary glands (author's transl)].

作者信息

Bienengräber V

出版信息

Arch Geschwulstforsch. 1978;48(1):35-49.

PMID:207234
Abstract

The mucoepidermoid tumor of the salivary glands is relatively rare; its ultrastructure is analysed on the basis of four cases. Three secretory tumour cells can be differentiated: one tumour cell with mucous secretion and two tumour cells with abortive secretion which are different in structure. The dysregulated and abortive secretion is due to a defective functional differentiation and defective innervation of tumour cells. Further characteristic tumour cells without secretion are: epidermoid cells, myoepithelial cells and clear cells. The variety of the tumour cells in the tissue is due to the broad cytogenic prospection of acinar and tubular epithelium of the salivary glands. Recommendations are given for practical electron-microscopic diagnosis by means of typical leading elements of the structure. The author tries to assess the gravity of the mucoepidermoid tumour by ultramicroscopic findings. The tumour is classified as potentially malignant. Therapeutic aspects are discussed dependent upon this grading.

摘要

涎腺黏液表皮样肿瘤相对少见;基于4例病例对其超微结构进行分析。可区分出三种分泌性肿瘤细胞:一种为分泌黏液的肿瘤细胞,另外两种为结构不同的分泌不全的肿瘤细胞。分泌失调和分泌不全是由于肿瘤细胞功能分化缺陷和神经支配缺陷所致。其他无分泌功能的特征性肿瘤细胞有:表皮样细胞、肌上皮细胞和透明细胞。组织中肿瘤细胞的多样性源于涎腺腺泡和导管上皮广泛的细胞发生前景。借助结构典型的主要成分给出了实际电镜诊断的建议。作者试图通过超微结构检查结果评估黏液表皮样肿瘤的严重程度。该肿瘤被归类为潜在恶性肿瘤。并据此分级讨论了治疗方面的问题。

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