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Goblet cell carcinoid tumors of the appendix: An overview

机译:阑尾杯状细胞类癌:概述

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摘要

Goblet cell carcinoid is an enigmatic and rare tumor involving the appendix almost exclusively. Since its identification in 1969, understanding of this disease has evolved greatly, but issues regarding its histogenesis, nomenclature and management are still conjectural. The published English language literature from 1966 to 2009 was retrieved via PubMed and reviewed. Various other names have been used for this entity such as adenocarcinoid, mucinous carcinoid, crypt cell carcinoma, and mucin-producing neuroendocrine tumor, although none have been found to be completely satisfactory or universally accepted. The tumor is thought to arise from pluripotent intestinal epithelial crypt-base stem cells by dual neuroendocrine and mucinous differentiation. GCCs present in the fifth to sixth decade and show no definite sex predominance. The most common clinical presentation is acute appendicitis, followed by abdominal pain and a mass. Fifty percent of the female patients present with ovarian metastases. The histologic hallmark of this entity is the presence of clusters of goblet cells in the lamina propria or submucosa stain for various neuroendocrine markers, though the intensity is often patchy. Atypia is usually minimal, but carcinomatous growth patterns may be seen. These may be of signet ring cell type or poorly differentiated adenocarcinoma. Recently molecular studies have shown these tumors to lack the signatures of adenocarcinoma but they have some changes similar to that of ileal carcinoids (allelic loss of chromosome 11q, 16q and 18q). The natural history of GCC is intermediate between carcinoids and adenocarcinomas of the appendix. The 5-year overall survival is 76%. The most important prognostic factor is the stage of disease. Appendectomy and right hemicolectomy are the main modalities of treatment, followed by adjuvant chemotherapy in select cases. There is some debate about the surgical approach for these tumors, and a summary of published series and recommendations are provided.
机译:杯状细胞类癌是一种神秘且罕见的肿瘤,几乎只涉及阑尾。自从1969年被确认以来,对该病的认识有了很大的发展,但有关其组织发生,命名和管理的问题仍是推测性的。通过PubMed检索并审查了1966年至2009年出版的英语文献。尽管发现没有一个完全令人满意或被普遍接受的名称,但各种其他名称已用于该实体,例如腺类癌,粘液性类癌,隐窝细胞癌和产生粘蛋白的神经内分泌肿瘤。该肿瘤被认为是由双能神经内分泌和粘液分化引起的多能性肠上皮隐窝基干细胞引起的。海湾合作委员会存在于第五个到第六个十年,并且没有明确的性别优势。最常见的临床表现是急性阑尾炎,其次是腹痛和肿块。 50%的女性患者出现卵巢转移。该实体的组织学特征是,对于各种神经内分泌标记物,固有层或粘膜下层染色中存在杯状细胞簇,尽管强度通常是不规则的。非典型性症状通常很少,但可以看到癌性生长模式。这些可能是印戒细胞型或分化差的腺癌。最近的分子研究表明,这些肿瘤缺乏腺癌的特征,但它们具有与回肠类癌相似的变化(11q,16q和18q染色体等位基因丢失)。 GCC的自然病史介于阑尾类癌和腺癌之间。 5年总生存率为76%。最重要的预后因素是疾病的阶段。阑尾切除术和右半结肠切除术是主要的治疗方式,随后在某些情况下进行辅助化疗。关于这些肿瘤的手术方法存在一些争议,并提供了已发表系列和建议的摘要。

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