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婴儿期肠系膜囊肿:临床表现与治疗

Mesenteric cyst in infancy: presentation and management.

作者信息

Belhassen Samia, Meriem Braiki, Rachida Laamiri, Nahla Kechiche, Saida Hidouri, Imed Krichen, Sana Mosbahi, Amine Ksiaa, Lassad Sahnoun, Mongi Mekki, Mohsen Belguith, Abdellatif Nouri

机构信息

University Hospital of Monastir, Department of Pediatric Surgery, Monastir, Tunisia.

Research Laboratory LR 12SP13, School of Medicine of Monastir University of Monastir, Tunisia.

出版信息

Pan Afr Med J. 2017 Mar 31;26:191. doi: 10.11604/pamj.2017.26.191.11476. eCollection 2017.

Abstract

Mesenteric cysts are documented as a rare entity in pediatric population. They are considered as benign intra-abdominal tumors with an unknown etiology. Symptoms are not specific and knowledge of such condition is essential in order to establish a proper management. We report three pediatrics cases of mesenteric cysts managed between 2000 and 2009 in the pediatric surgery Department of Monastir College Hospital. We described the clinical, radiological and operative findings. Two males and a female were managed (age range: 10 days-5years, mean age: 6,3years). Two patients were presented with an intestinal obstruction. A preoperative diagnosis was made basing on imaging. Thus, abdominal ultrasonography was performed in all of our reported cases and showed a cystic mass in all cases. The cystic nature of the mass, its margins and its extension were better described on tomographic images. The mesenteric cyst was completely and successfully removed in all cases. The histopathological report confirmed the diagnosis and showed a multiloculated cyst with columnar mesothelial lining, without any defined muscular layer or cellular atypia and without any evidence of malignancy. The children were evaluated post-operatively with a mean follow-up of 2 years and a half. No recurrence was noted in our patients during the follow-up period. It is known that clinical features are not specific of such anomaly but once the diagnosis is made, the complete surgical removal of the cyst remains the treatment of choice with excellent outcomes.

摘要

肠系膜囊肿在儿科人群中被记录为一种罕见疾病。它们被视为病因不明的良性腹腔内肿瘤。症状不具有特异性,了解这种疾病对于制定恰当的治疗方案至关重要。我们报告了2000年至2009年在莫纳斯提尔大学医院儿科外科治疗的3例肠系膜囊肿患儿病例。我们描述了临床、放射学和手术所见。接受治疗的有2名男性和1名女性(年龄范围:10天至5岁,平均年龄:6.3岁)。2例患者表现为肠梗阻。术前诊断基于影像学检查。因此,我们报告的所有病例均进行了腹部超声检查,所有病例均显示有囊性肿块。断层图像能更好地描述肿块的囊性特征、边界及其范围。所有病例中的肠系膜囊肿均被完整且成功地切除。组织病理学报告证实了诊断,显示为一个多房性囊肿,内衬柱状间皮,无明确的肌层或细胞异型性,也无任何恶性证据。对患儿进行了术后评估,平均随访时间为两年半。在随访期间,我们的患者未出现复发情况。众所周知,这种异常的临床特征不具有特异性,但一旦确诊,完整手术切除囊肿仍是首选治疗方法,且效果极佳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c8f/5483360/03577f51b8ab/PAMJ-26-191-g001.jpg

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