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黏液性囊腺瘤所致巨大附属器黏液囊肿

Giant Appendicular Mucocele Due to Mucinous Cystadenoma.

作者信息

Sertkaya Mehmet, Emre Arif, Pircanoglu Eyüp Mehmet, Peker Onur, Cengiz Emrah, Karaagaç Mustafa

机构信息

Department of General Surgery, Kahramanmaraş Sütçü İmam Üniversitesi, Kahramanmaraş, Turkey.

Department of General Surgery, Necip Fazil State Hospital, Kahramanmaraş, Turkey.

出版信息

Euroasian J Hepatogastroenterol. 2016 Jul-Dec;6(2):186-189. doi: 10.5005/jp-journals-10018-1197. Epub 2016 Dec 1.

Abstract

UNLABELLED

Mucocele of the appendix is a rare clinicopathological entity simulating acute appendicitis. The most common form of the mucocele is cystadenoma, which is characterized by luminal dilatation producing large amounts of mucin. We present a new case of a giant mucocele of appendix with mucinous cystadenoma. A 61-year-old female was admitted with complaints of severe lower right quadrant pain. Ultrasonography and computed tomography (CT) suggested that it was a mucocele, but due to severity of pain, she underwent an emergency operation. Fortunately, without a perforation, it was a giant mucocele and the operation was terminated with an uneventful appendectomy with segmental cecal resection. The histopathological evaluation of the specimen reported to be a mucocele with mucinous cystadenoma with negative surgical margins. The patient was discharged postoperative 6th day, and a control colonoscopy and abdominal CT was planned for 6 months following surgery. Appendicular mucocele is rare and difficult to diagnose preoperatively, and sometimes it may be of large size which increases the risk of perforation. Pseudomyxoma peritonei (PP) is the most feared complication of mucocele perforation. Appendectomy with negative margins is a requirement for adequate treatment for most cases. Utmost care should be taken during surgery to avoid perforation of mucocele.

HOW TO CITE THIS ARTICLE

Sertkaya M, Emre A, Pircanoglu EM, Peker O, Cengiz E, Karaagaç M. Giant Appendicular Mucocele Due to Mucinous Cystadenoma. Euroasian J Hepato-Gastroenterol 2016;6(2):186-189.

摘要

未标注

阑尾黏液囊肿是一种罕见的临床病理实体,类似急性阑尾炎。黏液囊肿最常见的形式是囊腺瘤,其特征为管腔扩张并产生大量黏液。我们报告一例伴有黏液性囊腺瘤的巨大阑尾黏液囊肿新病例。一名61岁女性因严重右下象限疼痛入院。超声和计算机断层扫描(CT)提示为黏液囊肿,但由于疼痛剧烈,她接受了急诊手术。幸运的是,囊肿未穿孔,为巨大黏液囊肿,手术以阑尾切除术加部分盲肠切除术顺利完成。标本的组织病理学评估报告为伴有黏液性囊腺瘤的黏液囊肿,手术切缘阴性。患者术后第6天出院,计划术后6个月进行结肠镜检查和腹部CT复查。阑尾黏液囊肿罕见,术前难以诊断,有时囊肿可能很大,增加了穿孔风险。腹膜假黏液瘤(PP)是黏液囊肿穿孔最可怕的并发症。大多数病例充分治疗需要切缘阴性的阑尾切除术。手术期间应格外小心,避免黏液囊肿穿孔。

如何引用本文

Sertkaya M, Emre A, Pircanoglu EM, Peker O, Cengiz E, Karaagaç M. 黏液性囊腺瘤导致的巨大阑尾黏液囊肿。《欧亚肝脏胃肠病学杂志》2016年;6(2):186 - 189。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf62/5578593/604f71f57ed0/ejohg-06-186-g001.jpg

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