Clinicopathological and Perioperative Outcome of Appendiceal Tumors: Case Review of 31 Patients.

Spartan medical research journal Pub Date : 2020-10-30
Haroutioun Boyajian, Vanessa Majeski, Alicia Flores, David Sturtz, Fadi Baidoun, Mohammed Dughayli
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Abstract

Introduction: Neoplasms of the appendix are quite rare and found in approximately 1% of appendectomy specimens. These neoplasms have been pathologically categorized into various subgroups depending on cell of origin, and surgical treatment varies according to histological subtype and disease stage.

Purpose: The purpose of this case series review was to evaluate the clinicopathological presentation and survival outcome of a sample of patients with appendiceal tumors.

Methods: Before data collection, this project design was approved by the authors' institutional review board. Pathology records at our institution were reviewed for cases of appendiceal tumors from January 2007 to December 2016. A total of 31 patients were identified over this 10-year period. Retrospective data collection included patient demographics, presenting symptoms, tumor size, histologic diagnosis, initial and secondary management, perioperative and postoperative outcome, and survival benefits.

Results: Thirty one patients with four different appendiceal tumor subtypes were included in the study: Mucinous Cystadenoma, Mucinous Adenocarcinoma, Goblet Cell, and Carcinoid. The sample was comprised of 17 women (54.8%) and 14 men (45.2%) with an overall mean age of 50.1 (SD = 22.3). Subgroups of 13 (42%) patients had Carcinoid tumor, 12 (39%) had Mucinous Cystadenoma, four (13%) had Goblet cell tumor, and two (6%) had Mucinous Adenocarcinoma. The stage at presentation and tumor size also varied by histologic subtype. The most common presenting symptom was abdominal pain (64.5%), followed by a radiological identified mass (12.9%). Overall, 27 (87.1%) patients survived, and four (12.9%) were deceased.

Conclusions: The findings from this case series review provides a retrospective analysis of appendiceal tumor characteristics, follow up, and survival. Based on these results, the prognosis and management of patients with these tumors should be based on the histologic subtype and the extent of their disease.

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阑尾肿瘤的临床病理和围手术期结果:31例患者的病例回顾
简介阑尾肿瘤相当罕见,约占阑尾切除术标本的 1%。根据起源细胞的不同,这些肿瘤在病理学上被分为不同的亚组,手术治疗也因组织学亚型和疾病分期而异。目的:本病例系列回顾旨在评估阑尾肿瘤患者的临床病理表现和生存结果:在收集数据之前,该项目设计已获得作者所在机构审查委员会的批准。我们查阅了本院2007年1月至2016年12月阑尾肿瘤病理记录。在这 10 年间,共发现了 31 例患者。回顾性数据收集包括患者人口统计学特征、主要症状、肿瘤大小、组织学诊断、初始和辅助治疗、围手术期和术后结果以及生存获益:研究共纳入了31名患有四种不同亚型阑尾肿瘤的患者:粘液性囊腺瘤、粘液性腺癌、鹅口疮细胞和类癌。样本中有 17 名女性(54.8%)和 14 名男性(45.2%),总平均年龄为 50.1 岁(SD = 22.3)。13名患者(42%)患有类癌,12名患者(39%)患有粘液性囊腺瘤,4名患者(13%)患有鹅口疮细胞瘤,2名患者(6%)患有粘液腺癌。不同组织学亚型的患者发病时的分期和肿瘤大小也各不相同。最常见的发病症状是腹痛(64.5%),其次是放射学发现的肿块(12.9%)。总体而言,27 例(87.1%)患者存活,4 例(12.9%)死亡:本病例系列回顾性研究对阑尾肿瘤的特征、随访和生存情况进行了回顾性分析。根据这些结果,这些肿瘤患者的预后和治疗应根据其组织学亚型和病变范围而定。
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