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阑尾黏液性肿瘤:一种分类尚不明确的实体。病例报告。

Appendiceal mucinous neoplasms: an uncertain nosological entity. Report of a case.

作者信息

Agrusa A, Romano G, Galia M, Cucinella G, Sorce V, Di Buono G, Agnello F, Amato G, Gulotta G

出版信息

G Chir. 2016 Mar-Apr;37(2):86-9. doi: 10.11138/gchir/2016.37.2.086.

Abstract

INTRODUCTION

Appendiceal mucocele is a relatively rare condition characterized by progressive dilation of the appendix caused by intraluminal accumulation of mucoid substance. Its incidence is 0.07 - 0,63% of all appendectomies performed.

CASE REPORT

We report the case of a 70-year-old man who came to our observation with gravative pain in right lower abdominal region. A computed tomography abdominal scan revealed a cystic/tubular structure like an appendicular mass with wall enhancement but without calcifications suggestive of a mucocele. Into peritoneal cavity we found profuse mucinous material with a 1,5 cm size parietal nodule. We also identified a free perforation of the cecum with consensual spillage of gelatinous material mimicking a pseudomyxoma peritonei. We decided to perform a right hemicolectomy with excision of peritoneal lesion.

DISCUSSION

The controversy in the pathologic terminology can give rise to a clinical dilemma in terms of the management and follow-up plans. For mucosal hyperplasia and cystadenoma simple appendectomy is curative. Only in case of large base of implantation it may be necessary the resection of the ileum and caecum or right hemicolectomy. In case of mucinous cystoadenocarcinoma authors perform a right hemicolectomy.

CONCLUSION

Appendiceal mucinous neoplasms are different pathological entities. The correct surgical management depends on size and location of lesion. A preoperative diagnosis is obviously needed in order to perform the correct treatment. CT abdominal scan is the better diagnostic tool, but different authors show their inability to reach a preoperative diagnosis in the larger majority of cases.

摘要

引言

阑尾黏液囊肿是一种相对罕见的病症,其特征为阑尾因腔内黏液物质积聚而逐渐扩张。在所有阑尾切除术中,其发病率为0.07%-0.63%。

病例报告

我们报告一例70岁男性患者,因右下腹部疼痛前来我院就诊。腹部计算机断层扫描显示一个囊状/管状结构,类似阑尾肿物,壁有强化但无钙化,提示为黏液囊肿。在腹腔内我们发现大量黏液性物质以及一个1.5厘米大小的壁层结节。我们还发现盲肠有一个游离穿孔,伴有类似腹膜假黏液瘤的胶冻状物质溢出。我们决定行右半结肠切除术并切除腹膜病变。

讨论

病理学术语的争议可能会导致在治疗和随访计划方面出现临床困境。对于黏膜增生和囊腺瘤,单纯阑尾切除术可治愈。仅在植入基部较大的情况下,可能需要切除回肠和盲肠或行右半结肠切除术。对于黏液性囊腺癌,作者主张行右半结肠切除术。

结论

阑尾黏液性肿瘤是不同的病理实体。正确的手术治疗取决于病变的大小和位置。显然需要进行术前诊断以便实施正确的治疗。腹部CT扫描是较好的诊断工具,但不同作者表明在大多数病例中他们无法做出术前诊断。

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