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皮肤神经内分泌癌病例报告:组织化学与电子显微镜研究

Case report of neuroendocrine carcinoma of the skin, histochemical and electron microscopic study.

作者信息

Nakashima N, Goto K, Takeuchi J, Maeda H

出版信息

Virchows Arch A Pathol Anat Histopathol. 1983;401(3):261-73. doi: 10.1007/BF00734844.

DOI:10.1007/BF00734844
PMID:6415907
Abstract

A rare case of neuroendocrine carcinoma of the skin in a 83-year-old male Japanese was reported. Histological, electron microscopical and cytological studies were performed on the surgically removed tumor tissue and the cultured tissue. The tumor occurred at the junction of the dermis and subcutaneous tissue of the right elbow, and spread to the right brachial region and axilla. Histologically, the tumor consisted mostly of small anaplastic cells, closely resembling lymphocytes. They showed a characteristic uniformity without rosette or trabecular formation in the usual histological sections, but an epithelial-like arrangement of tumor cells was readily observable both in the tissue culture and imprint preparations. Grimelius' stain was weakly positive in the periphery of the cytoplasm. Neuron Specific Enolase (NSE) activity was high both in the serum and in the tumor mass. No gastro-entero-pancreatic hormones were detected. Electron microscopically, membrane-bound granules of neurosecretory type, 90 to 170 nm in diameter were observed in the cytoplasm. These granules were characteristically distributed along the periphery of cytoplasm beneath the plasma membrane and in clusters in the cell processes. The tumor cells had sparse rudimentary desmosome-like junctions and a few cytoplasmic finger-like projections. Either a neurogenic or APUD cell origin of the tumor was suspected. The serum NSE value, suggesting to be a neurogenic origin before the histological examination in the present case, is considered to be a valuable marker substance for screening and therapeutic monitoring of neurogenic tumors.

摘要

报告了一例83岁日本男性皮肤神经内分泌癌的罕见病例。对手术切除的肿瘤组织和培养组织进行了组织学、电子显微镜和细胞学研究。肿瘤发生于右肘真皮与皮下组织交界处,并蔓延至右肱部及腋窝。组织学上,肿瘤主要由小的间变细胞组成,与淋巴细胞极为相似。在常规组织切片中,它们表现出特征性的一致性,无玫瑰花结或小梁形成,但在组织培养和印片标本中均易于观察到肿瘤细胞呈上皮样排列。Grimelius染色在细胞质周边呈弱阳性。血清和肿瘤块中的神经元特异性烯醇化酶(NSE)活性均较高。未检测到胃肠胰激素。电子显微镜下,在细胞质中观察到直径90至170nm的神经分泌型膜结合颗粒。这些颗粒特征性地分布在质膜下方的细胞质周边以及细胞突起的簇中。肿瘤细胞具有稀疏的原始桥粒样连接和一些细胞质指状突起。怀疑肿瘤起源于神经源性或APUD细胞。在本病例中,血清NSE值在组织学检查前提示为神经源性起源,被认为是神经源性肿瘤筛查和治疗监测的一种有价值的标志物。

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引用本文的文献

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[Clinical aspects and therapy of Merkel cell tumor--report of 4 personal cases and review of the literature].默克尔细胞肿瘤的临床特征与治疗——4例个人病例报告及文献综述

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"CHROMAFFIN" CELL: ELECTRON MICROSCOPIC IDENTIFICATION IN THE HUMAN DERMIS.“嗜铬”细胞:人真皮中的电子显微镜鉴定
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