Barbash Daniel, Trivedi Aakash A, Yang James Y, Nguyen Richard B, Huribal John C, Zuberi Jamshed, Elsawy Osama, Wessner Scott
Department of Surgery, St. Joseph's University Medical Center, Paterson, New Jersey, USA.
Department of Surgery, St. George's University, Great River, New York, USA.
J Surg Case Rep. 2022 Jul 31;2022(7):rjac356. doi: 10.1093/jscr/rjac356. eCollection 2022 Jul.
Goblet cell carcinoid (GCC) tumor is a rare appendiceal carcinoma that has had several names throughout its history. Often found incidentally on pathology following an appendectomy, treatment includes a right hemicolectomy and possible adjuvant chemotherapy. Survival rate has been shown to be correlated with the histological features. Here, we report a 45-year-old African American male who presented with signs and symptoms consistent with acute appendicitis, but was ultimately diagnosed with GCC. After undergoing a right hemicolectomy, he continues to undergo long-term surveillance with his oncologist. Due to the rarity of this tumor, we describe the history of GCC and our recommendations for surgical and long-term management.
杯状细胞类癌(GCC)肿瘤是一种罕见的阑尾癌,在其历史上有过多个名称。通常在阑尾切除术后的病理检查中偶然发现,治疗方法包括右半结肠切除术和可能的辅助化疗。生存率已显示与组织学特征相关。在此,我们报告一名45岁的非裔美国男性,他表现出与急性阑尾炎一致的体征和症状,但最终被诊断为GCC。在接受右半结肠切除术后,他继续接受肿瘤学家的长期监测。由于这种肿瘤的罕见性,我们描述了GCC的病史以及我们对手术和长期管理的建议。