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儿童腹膜包虫囊肿:罕见包虫病定位的病例系列。

Peritoneal Hydatid Cysts in Children: A Case Series of Rare Echinococcosis Localization.

机构信息

Research Laboratory Children Malformative and Tumoral Pathology LR12SP13, Department of Pediatric Surgery, University of Monastir, Monastir, Tunisia.

出版信息

Iran J Med Sci. 2021 Jan;46(1):68-72. doi: 10.30476/ijms.2020.82004.0.

DOI:10.30476/ijms.2020.82004.0
PMID:33487794
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7812502/
Abstract

Peritoneal hydatid cysts are rare in children even in endemic areas. The primary or secondary origin of this site remains controversial, especially in children. Secondary peritoneal hydatid cysts are mainly the result of spontaneous or traumatic rupture of concomitant liver cysts or the leakage of cystic content during surgery. The purpose of our study is to present the largest case series of peritoneal hydatidosis in children. In addition, we aimed to assess the clinical and paraclinical findings as well as the management of echinococcosis at this location in children. The present case series is a study of ten children with peritoneal hydatid cysts, who underwent surgical intervention between 2013 and 2018 in the Pediatric Surgery Department, University of Monastir (Monastir, Tunisia). The mean age of the children was six years. All children presented abdominal pain, and underwent ultrasonography and contrast-enhanced computed tomography of the abdomen. Two patients had been operated on for lung hydatid cysts six months prior to the study. In two cases, radiologic investigations revealed the presence of an uncomplicated hepatic hydatid cyst located in segments II and IV. All patients underwent surgery, of which four underwent laparoscopy. Post-surgery, all patients received albendazole for three months, and the follow-up period was uneventful. Currently, all patients are in good health. Peritoneal hydatid disease is frequently secondary to the rupture of a primary hepatic cyst. Diagnosis is performed by abdominal ultrasound, computed tomography, and a positive serology result. Open or laparoscopic excision can be combined with medical treatment.

摘要

儿童腹膜包虫囊肿很少见,即使在流行地区也是如此。该部位的原发性或继发性来源仍存在争议,尤其是在儿童中。继发性腹膜包虫囊肿主要是由于并发肝囊肿自发性或外伤性破裂,或手术过程中囊内容物漏出所致。我们的研究目的是报告儿童腹膜包虫病的最大病例系列。此外,我们旨在评估儿童腹膜包虫病的临床和辅助检查结果以及该部位的治疗方法。本病例系列是对 2013 年至 2018 年期间在突尼斯莫纳斯提尔大学儿科外科接受手术干预的 10 例儿童腹膜包虫囊肿患者的研究。患儿平均年龄为 6 岁。所有患儿均有腹痛,并接受了腹部超声和增强 CT 检查。有 2 例患儿在研究前 6 个月曾因肺包虫囊肿而行手术治疗。在 2 例病例中,影像学检查显示存在位于 II 段和 IV 段的单纯性肝包虫囊肿。所有患者均接受手术治疗,其中 4 例患者接受腹腔镜手术。术后所有患者均接受阿苯达唑治疗 3 个月,随访期间无不良事件发生。目前,所有患儿均身体健康。腹膜包虫病常继发于原发性肝囊肿破裂。诊断方法是腹部超声、CT 和阳性血清学结果。开放性或腹腔镜切除可与药物治疗联合应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/0a25c105a043/IJMS-46-68-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/fd1ee530726e/IJMS-46-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/ebdfebbd592d/IJMS-46-68-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/0a25c105a043/IJMS-46-68-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/fd1ee530726e/IJMS-46-68-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/ebdfebbd592d/IJMS-46-68-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a46/7812502/0a25c105a043/IJMS-46-68-g003.jpg

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以腹胀为表现的原发性腹膜包虫囊肿:一例报告
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Primary cystic echinococcosis of the peritoneum: a case report.腹膜原发性囊型包虫病 1 例报告。
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