Suppr超能文献

[阑尾、结肠和直肠的神经内分泌肿瘤:当前外科手术要点]

[Neurendocrine tumours of the appendix, colon and rectum: current surgical aspects].

作者信息

Rosato Lodovico, De Tomaa Giorgio, Mondini Guido, Bertone Paola, Fornari Francesca, Orlassino Renzo

机构信息

Dipartimento di Chirurgia, Ospedale di Ivrea, Torino.

出版信息

Chir Ital. 2007 Jul-Aug;59(4):445-52.

Abstract

Neuroendocrine tumours (NET) are a heterogeneous group of neoplasms deriving from a system of diffuse neuroendocrine cells in organs and tissues, defined as the "diffuse neuroendocrine system". Over the period from 1996 to 2005 42 patients with gastroenteropancreatic (GEP) NET were observed (M.F ratio: 1.5:1; mean age 58 years; > 60 years for all localisations except the appendix [< 39 years]). Twenty-three were tumours of the appendix, colon and rectum, corresponding to 55% of all those affecting the digestive tract: 8 appendix (35%), 6 right colon (26%), 4 left colon (17%) and 5 rectum (22%). The NET diagnosis was formulated in all cases on the basis of histological and immunohistochemical examinations. The mean follow-up period was 5 years (range: 1-10). In the RO-RI cases no relapses occurred and those who were not disease-free were treated with somatostatin analogues and/or chemotherapy. NET of the appendix, colon and rectum are rare, despite being the most frequent among the GEP tumours, and are difficult to diagnose, and therefore sometimes pose problems of surgical therapy, which, when performed in time, may be curative. NET of the appendix measuring <2 cm, localised in the distal part without local infiltration, can be treated by simple appendicectomy and removal of the mesenteriole; otherwise, right hemicolectomy is indicated. The surgical treatment of tumours of the colon, except for well differentiated cases measuring <2 cm with a pedunculate structure such as to allow safe endoscopic removal, consists in radical hemicolectomy with lymphadenectomy. Carcinoids of the rectum measuring <1 cm and 1 cm to 2 cm, in the absence of other negative prognostic factors, can be treated locally by transanal endoscopic microsurgery (TEM) or minimally invasive transanal surgery (MITAS). Tumours measuring >2 cm or presenting muscular invasion and/or lymph-node metastases (malignant carcinoids), regardless of tumour diameter, are submitted to radical operations, as in the case of carcinoma of the rectum. Extensive disease which is no longer curable with surgery alone is treated with chemotherapy and bio-chemotherapy, but it is above all treatment with somatostatin analogues that plays a major role in symptom control.

摘要

神经内分泌肿瘤(NET)是一组异质性肿瘤,起源于器官和组织中的弥漫性神经内分泌细胞系统,该系统被定义为“弥漫性神经内分泌系统”。在1996年至2005年期间,观察到42例胃肠胰(GEP)NET患者(男女比例为1.5:1;平均年龄58岁;除阑尾外,所有部位患者年龄均>60岁[阑尾患者年龄<39岁])。23例为阑尾、结肠和直肠肿瘤,占所有消化道肿瘤患者的55%:8例阑尾肿瘤(35%),6例右半结肠肿瘤(26%),4例左半结肠肿瘤(17%),5例直肠肿瘤(22%)。所有病例均根据组织学和免疫组化检查做出NET诊断。平均随访期为5年(范围:1 - 10年)。在RO - RI病例中未发生复发,对未达到无病状态的患者采用生长抑素类似物和/或化疗进行治疗。阑尾、结肠和直肠的NET尽管是GEP肿瘤中最常见的,但较为罕见,且难以诊断,因此有时会带来手术治疗方面的问题,不过及时进行手术可能治愈。阑尾NET直径<2 cm,位于远端且无局部浸润,可通过单纯阑尾切除术及切除系膜进行治疗;否则,建议行右半结肠切除术。结肠肿瘤的手术治疗,除了分化良好、直径<2 cm且具有带蒂结构从而可通过安全的内镜切除的病例外,均包括根治性半结肠切除术及淋巴结清扫术。直肠类癌直径<1 cm以及1 cm至2 cm,在无其他不良预后因素的情况下,可通过经肛门内镜显微手术(TEM)或微创经肛门手术(MITAS)进行局部治疗。直径>2 cm或出现肌层浸润和/或淋巴结转移的肿瘤(恶性类癌),无论肿瘤直径大小,均需进行根治性手术,如同直肠癌的情况。无法通过手术治愈的广泛性疾病采用化疗和生物化疗进行治疗,但最重要的是,生长抑素类似物治疗在症状控制方面发挥着主要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验