低级别阑尾黏液性肿瘤和阑尾子宫内膜异位症。
Low-grade appendiceal mucinous neoplasm and endometriosis of the appendix.
机构信息
University of Miami Miller School of Medicine, 1475 NW 12th Ave, 3rd Flr, Miami, FL, 33136, USA.
Department of Surgical Oncology, Sylvester Comprehensive Cancer Center, Miami, FL, 33136, USA.
出版信息
World J Surg Oncol. 2017 Dec 19;15(1):226. doi: 10.1186/s12957-017-1294-1.
BACKGROUND
A distended, mucous-filled appendix is known as an appendiceal mucocele. They are a rare form of an appendiceal mass and develop from both benign and malignant processes. Mucoceles can develop secondarily to an obstruction, such as from a fecalith, scarring or, rarely, endometriosis. Only 12 cases of non-neoplastic appendiceal mucoceles caused by endometriosis have been previously described. The association between neoplastic appendiceal mucoceles in the presence of endometriosis is described for the first time in this report.
CASE PRESENTATION
A 57-year-old woman presented with a chief complaint of worsening abdominal pain over the past 3 months. Imaging studies revealed an appendiceal mass. Laparoscopic evaluation confirmed an appendiceal mucocele, and the patient underwent complete appendectomy. No evidence of mucinous or endometrial deposits were present within the abdominal cavity. Pathological diagnosis revealed low-grade appendiceal mucinous neoplasm (LAMN) with evidence of endometriosis within the muscularis propria of the appendix. The patient recovered without complications and her abdominal pain completely resolved.
CONCLUSIONS
Endometriosis of the appendix is a rare manifestation and is most often identified as an incidental finding. Endometriosis leading to an obstructive mucocele of the appendix is an exceedingly rare finding, having only been described 12 times in the medical literature. LAMN in the presence of endometriosis of the appendix is described for the first time in this report. The association between appendiceal neoplasms in the presence of endometriosis requires further research in order to optimize operative treatment.
背景
充满黏液的扩张阑尾被称为阑尾黏液囊肿。它们是阑尾肿块的一种罕见形式,由良性和恶性过程发展而来。黏液囊肿可继发于梗阻,如粪石、瘢痕或罕见的子宫内膜异位症。以前仅描述过 12 例由子宫内膜异位症引起的非肿瘤性阑尾黏液囊肿。本报告首次描述了存在子宫内膜异位症时的肿瘤性阑尾黏液囊肿的关联。
病例介绍
一名 57 岁女性因过去 3 个月腹痛加重就诊。影像学检查显示阑尾肿块。腹腔镜评估证实为阑尾黏液囊肿,患者接受了完整的阑尾切除术。腹腔内无黏液或子宫内膜沉积物的证据。病理诊断为低级别阑尾黏液性肿瘤(LAMN),阑尾肌层有子宫内膜异位症的证据。患者无并发症恢复,腹痛完全缓解。
结论
阑尾子宫内膜异位症是一种罕见的表现,通常作为偶然发现。导致阑尾阻塞性黏液囊肿的子宫内膜异位症极为罕见,仅在医学文献中描述过 12 次。本报告首次描述了在阑尾子宫内膜异位症存在的情况下发生的 LAMN。存在子宫内膜异位症的阑尾肿瘤之间的关联需要进一步研究,以优化手术治疗。