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首页> 外文期刊>The Journal of laryngology and otology. >Small cell neuroendocrine carcinoma of the nasal cavity and paranasal sinuses.
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Small cell neuroendocrine carcinoma of the nasal cavity and paranasal sinuses.

机译:鼻腔和鼻旁窦的小细胞神经内分泌癌。

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INTRODUCTION: Small cell neuroendocrine carcinoma (SNEC) of the sinonasal tract is a rare disease. OBJECTIVE: Report a descriptive study of a relatively large cohort of SNEC of the nasal cavity and paranasal sinuses. METHOD: The medical records of 21 patients presenting with nasal and paranasal SNEC to various French hospitals, from 1989 to 2003, were analysed to determine the clinical features and current treatment of the disease. RESULTS: Patient data were obtained from eight French hospitals. Twelve of the patients were male and nine were female, with a mean age at presentation of 55 years (range: 27 to 79 years). Patients' staging for nasal cavity malignancy was: T1, four; T2, three; T3, one; T4, 13; N0, 18; N2, three; M0, 20; and M1, one. None of the patients suffered from SNEC of the sinonasal tract with ectopic hormone production. Immunohistochemistry proved useful for diagnosis in 20 cases. Twelve cases were positive for cytokeratin, 14 for chromogranin, eight for neuron-specific enolase and 11 for neuron-specific synaptophysin. One patient had an adenocarcinoma and an inverted papilloma associated with neuroendocrine carcinoma. Patients underwent surgery (11 cases), radiotherapy (14 cases) and chemotherapy (12 cases). Recurrence occurred in 10 cases. Five patients had visceral metastases or cervical lymph node involvement. Nine of the patients died within four years of onset of the disease. CONCLUSION: Small cell neuroendocrine carcinoma of the sinonasal tract is an uncommon neoplasm with aggressive clinical behaviour. Recurrence is frequent and the prognosis is poor. However, the current treatment of these neuroendocrine neoplasms varies widely.
机译:简介:鼻窦道小细胞神经内分泌癌(SNEC)是一种罕见的疾病。目的:报告一项描述性研究,涉及鼻腔和鼻旁窦的较大SNEC患者。方法:分析1989年至2003年在法国多家医院接受鼻和鼻旁SNEC治疗的21例患者的病历,以确定该疾病的临床特征和当前治疗方法。结果:患者数据来自八家法国医院。患者中有十二名男性,九名女性,平均年龄为55岁(范围:27至79岁)。患者鼻腔恶性肿瘤分期为:T1,4; T2,三个; T3,一; T4,13; N0,18; N2,三个; M0,20;和M1,一个。没有患者患有鼻窦SNEC并产生异位激素。免疫组织化学证明对20例诊断有用。 12例细胞角蛋白阳性,14例嗜铬粒蛋白阳性,8例神经元特异性烯醇化酶,11例神经元特异性突触素。一名患者患有腺癌和倒置性乳头状瘤并伴有神经内分泌癌。患者接受了手术(11例),放疗(14例)和化学疗法(12例)。复发发生10例。五例患者发生内脏转移或颈部淋巴结受累。该病发作的四年内有9名患者死亡。结论:鼻窦小细胞神经内分泌癌是一种罕见的肿瘤,具有侵袭性临床表现。复发频繁,预后差。但是,这些神经内分泌肿瘤的当前治疗方法差异很大。

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