Akbulut Sami
Sami Akbulut, Department of Surgery and Liver Transplant Institute, Inonu University Faculty of Medicine, Turgut Ozal Medical Center, Malatya 44280, Turkey.
World J Gastroenterol. 2015 Jan 14;21(2):675-87. doi: 10.3748/wjg.v21.i2.675.
To review the literature on idiopathic sclerosing encapsulating peritonitis (SEP), also known as abdominal cocoon syndrome.
The PubMed, MEDLINE, Google Scholar, and Google databases were searched using specific key words to identify articles related to idiopathic SEP. These key words were "sclerosing encapsulating peritonitis," "idiopathic sclerosing encapsulating peritonitis," "abdominal cocoon," and "abdominal cocoon syndrome." The search included letters to the editor, case reports, review articles, original articles, and meeting presentations published in the English-language literature from January 2000 to May 2014. Articles or abstracts containing adequate information about age, sex, symptom duration, initial diagnosis, radiological tools, and surgical approaches were included in the study. Papers with missing or inadequate data were excluded.
The literature search yielded 73 articles on idiopathic (primary) SEP published in 23 countries. The four countries that published the greatest number of articles were India (n = 21), Turkey (n = 14), China (n = 8) and Nigeria (n = 3). The four countries that reported the greatest number of cases were China (n = 104; 53.88%), India (n = 35; 18.13%), Turkey (n = 17; 8.80%) and Nigeria (n = 5; 2.59%). The present study included 193 patients. Data on age could be obtained for 184 patients (range: 7-87 years; mean ± SD, 34.7 ± 19.2 years), but were unavailable for nine patients. Of the 184 patients, 122 were male and 62 were female; sex data could not be accessed in the remaining nine patients. Of the 149 patients whose preoperative diagnosis information could be obtained, 65 (43.6%) underwent operations for abdominal cocoon, while the majority of the remaining patients underwent operations for a presumed diagnosis of intestinal obstruction and/or abdominal mass. Management information could be retrieved for 115 patients. Of these, 68 underwent excision + adhesiolysis (one laparoscopic); 24 underwent prophylactic appendectomy in addition to excision + adhesiolysis. Twenty patients underwent various resection and repair techniques along with excision + adhesiolysis. The remaining three patients were managed with antituberculosis therapy (n = 2) and immunosuppressive therapy (n = 1).
Idiopathic SEP is a rare disorder characterized by frequently recurring bouts of intestinal obstruction. Surgical therapy is the gold standard management strategy.
回顾关于特发性硬化性包裹性腹膜炎(SEP)的文献,该疾病也被称为腹茧症。
使用特定关键词在PubMed、MEDLINE、谷歌学术和谷歌数据库中进行检索,以识别与特发性SEP相关的文章。这些关键词为“硬化性包裹性腹膜炎”“特发性硬化性包裹性腹膜炎”“腹茧”和“腹茧症”。检索范围包括2000年1月至2014年5月在英文文献中发表的致编辑信、病例报告、综述文章、原创文章和会议报告。纳入研究的文章或摘要需包含关于年龄、性别、症状持续时间、初始诊断、影像学检查方法和手术方式的充分信息。数据缺失或不充分的论文被排除。
文献检索共得到23个国家发表的73篇关于特发性(原发性)SEP的文章。发表文章数量最多的四个国家分别是印度(n = 21)、土耳其(n = 14)、中国(n = 8)和尼日利亚(n = 3)。报告病例数最多的四个国家分别是中国(n = 104;53.88%)、印度(n = 35;18.13%)、土耳其(n = 17;8.80%)和尼日利亚(n = 5;2.59%)。本研究纳入了193例患者。184例患者(范围:7 - 87岁;平均±标准差,34.7±19.2岁)可获取年龄数据,9例患者无法获取。在这184例患者中,122例为男性,62例为女性;其余9例患者无法获取性别数据。在可获取术前诊断信息的149例患者中,65例(43.6%)因腹茧症接受手术,其余大多数患者因疑似肠梗阻和/或腹部肿块接受手术。115例患者可获取治疗信息。其中,68例接受切除 + 粘连松解术(1例为腹腔镜手术);24例在切除 + 粘连松解术基础上接受预防性阑尾切除术。20例患者接受了各种切除和修复技术以及切除 + 粘连松解术。其余3例患者分别接受抗结核治疗(n = 2)和免疫抑制治疗(n = 1)。
特发性SEP是一种罕见疾病,其特征为肠梗阻频繁发作。手术治疗是金标准的治疗策略。