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喉神经内分泌肿瘤

Neuroendocrine neoplasms of the larynx.

作者信息

Overholt S M, Donovan D T, Schwartz M R, Laucirica R, Green L K, Alford B R

机构信息

Department of Otorhinolaryngology and Communicative Sciences, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Laryngoscope. 1995 Aug;105(8 Pt 1):789-94. doi: 10.1288/00005537-199508000-00004.

Abstract

Neuroendocrine neoplasms of the larynx are a rare group of tumors that include carcinoid tumor, atypical carcinoid tumor, and small cell carcinoma. These neoplasms pose interesting diagnostic, prognostic, and therapeutic dilemmas, and they are, as a whole, aggressive tumors with a tendency for local and distant spread. The authors of this study examined six new cases of laryngeal neuroendocrine neoplasms. One case manifested itself as a primary atypical carcinoid tumor and caused a "carcinoid syndrome." The remaining five cases were small cell carcinomas of the larynx. Histologic, immunocytochemical, DNA flow cytometric, and p53 studies were performed on all cases. The expression of neuron-specific enolase and chromogranin were the most useful markers in this group of tumors. Overexpression of p53 protein was present in the majority of cases, including the atypical carcinoid tumor. The implications of these studies for diagnosis, classification, and treatment are discussed.

摘要

喉神经内分泌肿瘤是一组罕见的肿瘤,包括类癌、非典型类癌和小细胞癌。这些肿瘤带来了有趣的诊断、预后和治疗难题,总体而言,它们是具有局部和远处扩散倾向的侵袭性肿瘤。本研究的作者检查了6例新的喉神经内分泌肿瘤病例。1例表现为原发性非典型类癌,并引发了“类癌综合征”。其余5例为喉小细胞癌。对所有病例进行了组织学、免疫细胞化学、DNA流式细胞术和p53研究。神经元特异性烯醇化酶和嗜铬粒蛋白的表达是这组肿瘤中最有用的标志物。大多数病例中存在p53蛋白过表达,包括非典型类癌。讨论了这些研究对诊断、分类和治疗的意义。

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