Otorhinolaryngology, Head and Neck Surgery Department, AHEPA University Hospital, Thessaloniki, Greece.
Head Neck. 2013 Jun;35(6):E187-93. doi: 10.1002/hed.22955. Epub 2012 Feb 6.
Neuroendocrine tumors are rare neoplasms arising from neural and epithelial origin.
The case records of 4 patients with the diagnosis of neuroendocrine laryngeal tumor were retrospectively reviewed. In this analysis of our medical records, we describe a series of 4 men with neuroendocrine laryngeal tumors treated in our department since 1994, including the first extremely aggressive and lethal laryngeal paraganglioma reported in the English-language literature. We also discuss the classification, the macro and microscopical characteristics, clinical and pathologic findings, and treatment of these neoplasms.
Although neuroendocrine laryngeal tumors account for approximately 1% of all neoplasms in the larynx, its majority represents very aggressive tumors showing a capacity for metastasis and portending poor outcome.
神经内分泌肿瘤是起源于神经和上皮的罕见肿瘤。
回顾性分析了 4 例神经内分泌性喉肿瘤患者的病例记录。在对我们的病历进行分析时,我们描述了自 1994 年以来在我们科室治疗的 4 例男性神经内分泌性喉肿瘤患者,其中包括在英语文献中首次报道的极侵袭性和致命性喉副神经节瘤。我们还讨论了这些肿瘤的分类、宏观和微观特征、临床和病理表现以及治疗方法。
虽然神经内分泌性喉肿瘤约占喉部所有肿瘤的 1%,但其大多数为侵袭性很强的肿瘤,具有转移能力,预后不良。