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阑尾黏液囊肿的外科治疗:一项系统评价及病例报告

Surgical treatment of mucocele of the appendix: a systematic review and case report.

作者信息

Saad Eltaib A, Elsamani Elamin Y, AbdElrahim Walid E, Elsiddig Kamal E, Khalil Eltahir A G

机构信息

Department of Surgery, Faculty of Medicine, University of Khartoum, Khartoum, Sudan.

Sudan Medical Specialization Board, Sudan.

出版信息

J Surg Case Rep. 2018 Jun 28;2018(6):rjy102. doi: 10.1093/jscr/rjy102. eCollection 2018 Jun.

Abstract

INTRODUCTION

Appendicular mucocele is a rare well-described clinico-pathological occurrence. It denotes an obstructive dilatation of the appendicular lumen by mucinous secretions.

CASE REPORT

A 60-year-old patient presented with right lower abdominal pain and nausea for 2 years. Abdominal CT scan suggested a diagnosis of a appendicular mucocele. Following informed consent, surgical exploration revealed a cystic mass arising from the body of the appendix with inflamed walls with no evidence of perforation. Simple appendectomy was performed as the caecum and the mesenteric nodes were free of pathological involvement. The final diagnosis of mucinous cystadenoma was confirmed by histopathology. Postoperative course was uneventful. The patient was in good health during a four years regular follow-up.

DISCUSSION

Appendicular mucocele is a rare disease with vague symptoms. Abdominal imaging is an important diagnostic tool, but histopathology is the standard for definitive diagnosis. Surgery for benign appendicular mucoceles has an excellent long-term prognosis.

摘要

引言

阑尾黏液囊肿是一种罕见但已被充分描述的临床病理现象。它指的是阑尾管腔因黏液性分泌物而发生的阻塞性扩张。

病例报告

一名60岁患者出现右下腹痛和恶心症状达2年。腹部CT扫描提示诊断为阑尾黏液囊肿。在获得知情同意后,手术探查发现一个源于阑尾体部的囊性肿物,其壁有炎症,无穿孔迹象。由于盲肠和肠系膜淋巴结无病理累及,遂行单纯阑尾切除术。组织病理学确诊为黏液性囊腺瘤。术后过程顺利。在四年的定期随访中,患者身体健康。

讨论

阑尾黏液囊肿是一种症状不明确的罕见疾病。腹部影像学是重要的诊断工具,但组织病理学是明确诊断的标准。良性阑尾黏液囊肿的手术具有良好的长期预后。

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