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结肠杯状细胞类癌:罕见中的罕见!一例病例报告及文献复习

Colonic Goblet Cell Carcinoid: Rarity of a Rarity! A Case Report and Review of Literature.

作者信息

Abdalla Abdalla Saad, Khan Kashuf Arooj, Shah Ahmed, Asaad Amira, Salter Victoria, Barron Marina, Eldruki Soad, Salih Victoria, Alowami Salem Omar

出版信息

Chirurgia (Bucur). 2020 Jan-Feb;115(1):102-111. doi: 10.21614/chirurgia.115.1.102.

Abstract

Goblet cell carcinoids (GCC) are extremelyrare neuroendocrine tumours, and characterised by their unique combination of two types of cancer cells âÃÂ" neuroendocrine (carcinoid) and epithelial (adeno-carcinoma). In spite of the fact that GCC is regarded as Neuro-Endocrine Tumour (NET), it does not illicit carcinoid syndrome. GCC usually arises in the appendix and accounting for less than 14% of all appendiceal tumours.Primary extra-appendiceal GCC have been reported as stomach, duodenum, small intestine, colon and rectum. The paper presents a rare case of GCC of the ascending colon in a 57-year-old male.

摘要

杯状细胞类癌(GCC)是极其罕见的神经内分泌肿瘤,其特征是两种癌细胞——神经内分泌(类癌)细胞和上皮(腺癌)细胞的独特组合。尽管GCC被视为神经内分泌肿瘤(NET),但它不会引发类癌综合征。GCC通常发生于阑尾,占所有阑尾肿瘤的比例不到14%。原发性阑尾外GCC已报道发生于胃、十二指肠、小肠、结肠和直肠。本文报告了一例57岁男性升结肠GCC的罕见病例。

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