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巨大乳糜性肠系膜囊肿及其成功摘除术:病例报告

Giant chylolymphatic mesenteric cyst and its successful enucleation: A case report.

作者信息

Al Booq Yousuf, Hussain Syed S, Elmy Mohamed

机构信息

Surgery Royal Commission Medical Center, Yanbu Al Sinayah, Saudi Arabia.

Surgery Royal Commission Medical Center, Yanbu Al Sinayah, Saudi Arabia.

出版信息

Int J Surg Case Rep. 2014;5(8):469-70. doi: 10.1016/j.ijscr.2014.05.008. Epub 2014 May 23.

Abstract

INTRODUCTION

Cysts of the mesentery are among surgical rarities. The clinical presentation is not characteristic and in addition, the preoperative imaging although suggestive is not diagnostic in this case ultrasound and CTscan was consistent with giant mesenteric cyst. In most cases, the diagnosis is confirmed after surgical exploration.

PRESENTATION OF CASE

A 42 yrs old male patient on exploratory laparotomy had a 14cm×10cm×10 cm cysts which was seen arising from the mesentery ofdistal jejunum 80cm from the duodeno jejunal flexure. The cyst was enucleated successfully from themesentery without entailing resection. The cyst contained milky white fluid consistent with a chylolymphatic cyst. The diagnosis was confirmed on histopathology which revealed a cyst wall with lymphoidaggregates. After 3 years of follow-up, the patient is doing well and there is no evidence of recurrence.

DISCUSSION

The cysts may be asymptomatic or maymanifest with abdominal pain, distension lump or intestinal obstruction. Our patient was symptomatic with mild and long standing abdominal pain. The definitive diagnosis of these lesions is difficult prior to surgical exploration as there are no pathognomonic symptoms or characteristic imaging findings.

CONCLUSION

Cysts of the mesentery are among surgical rarities. In most of the cases the diagnosis is confirmed after surgical exploration and removal of thecyst. We would like to emphasize the importance of successful enucleation of the cyst irrespective of its size due to its independent blood supply as opposed to enterogenous cyst which requires bowel resection and anastomosis.

摘要

引言

肠系膜囊肿是外科罕见疾病。其临床表现不具有特异性,此外,术前影像学检查虽有提示作用,但在此病例中超声和CT扫描结果仅提示为巨大肠系膜囊肿,并不具有诊断性。大多数情况下,需手术探查后才能确诊。

病例介绍

一名42岁男性患者接受剖腹探查术时,发现一个14厘米×10厘米×10厘米的囊肿,该囊肿起源于距十二指肠空肠曲80厘米处的空肠远端系膜。成功将囊肿从系膜上摘除,未进行切除。囊肿内含有乳白色液体,符合乳糜淋巴囊肿。组织病理学检查确诊,结果显示囊肿壁有淋巴聚集。经过3年随访,患者情况良好,无复发迹象。

讨论

囊肿可能无症状,也可能表现为腹痛、腹胀、肿块或肠梗阻。我们的患者有轻度且长期存在的腹痛症状。由于这些病变没有特征性症状或典型影像学表现,在手术探查前很难做出明确诊断。

结论

肠系膜囊肿是外科罕见疾病。大多数情况下,需手术探查并切除囊肿后才能确诊。我们想强调的是,由于囊肿有独立血供,与需要肠切除和吻合的肠源性囊肿不同,无论囊肿大小,成功摘除囊肿都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/4147644/adab7779dda7/gr1.jpg

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