Olson Doug E, Kim Yong-Woo, Donnelly Lane F
Department of Radiology, Cincinnati Children's Hospital Medical Center, MLC 5031, 3333 Burnet Ave., Cincinnati, OH 45229-3039, USA.
Pediatr Radiol. 2009 Jul;39(7):659-63; quiz 766-7. doi: 10.1007/s00247-008-1138-9. Epub 2009 Feb 3.
Approximately 0.04% of the general population will present with a complication related to Meckel diverticulum. The classic teaching is that symptomatic children with Meckel diverticulum present with painless rectal bleeding and are evaluated with a radionuclide scan. Our subjective experience is that we see children with Meckel diverticulum who present with abdominal pain and are evaluated by CT.
We reviewed the findings on CT in children with pathologically proven Meckel diverticulum to identify characteristic patterns of presentation.
Databases were searched (2004-2008) for all children who had a pathologic diagnosis of Meckel diverticulum and a CT scan performed prior to surgery. Demographics, pathology, and CT features were reviewed. CT features reviewed included: soft-tissue stranding, abnormal calcifications, bowel obstruction, free air, free peritoneal fluid, cystic mass, intussusception, obvious lead point, location, and whether a normal appendix was identified. The frequency of Meckel diverticulum encountered on CT scans was compared to that found during the same period of time on technetium pertechnetate studies.
The review identified 16 subjects (mean age 9.5 years, M:F 9:7). CT findings included: soft-tissue stranding in nine (56%), small-bowel obstruction (SBO) in nine (56%), intussusception in three (19%), free fluid in ten (63%), cystic mass in four (25%), calcification in none (0%), free air in one (6%), and no abnormalities in two (13%). A normal appendix was identified in only five children (31%). There were three basic patterns of presentation of abnormalities: SBO only in five, intussusception with SBO in three, or cystic mass with inflammatory stranding in four (one with SBO). Also, 2.3 times more Meckel diverticulum was encountered on CT than on technetium pertechnetate studies.
Meckel diverticulum is currently more commonly encountered in children on CT performed for abdominal pain than on technetium pertechnetate studies. There are three categories of appearance on CT: SBO only, intussusception, or a cystic inflammatory mass.
普通人群中约0.04%会出现与梅克尔憩室相关的并发症。传统观点认为,有症状的梅克尔憩室患儿表现为无痛性直肠出血,并通过放射性核素扫描进行评估。我们的主观经验是,我们见到的梅克尔憩室患儿表现为腹痛,并通过CT进行评估。
我们回顾了经病理证实的梅克尔憩室患儿的CT检查结果,以确定其特征性表现模式。
检索数据库(2004 - 2008年),查找所有经病理诊断为梅克尔憩室且在手术前进行了CT扫描的患儿。回顾其人口统计学资料、病理学及CT特征。回顾的CT特征包括:软组织条索影、异常钙化、肠梗阻、游离气体、腹腔游离液体、囊性肿块、肠套叠、明显的引导点、位置以及是否发现正常阑尾。将CT扫描中梅克尔憩室的检出频率与同期锝高锝酸盐检查中发现的频率进行比较。
该回顾纳入了16例受试者(平均年龄9.5岁,男∶女 = 9∶7)。CT表现包括:9例(56%)有软组织条索影,9例(56%)有小肠梗阻(SBO),3例(19%)有肠套叠,10例(63%)有游离液体,4例(25%)有囊性肿块,无(0%)有钙化,1例(6%)有游离气体,2例(13%)无异常。仅5例患儿(31%)发现正常阑尾。异常表现有三种基本模式:仅SBO 5例,肠套叠合并SBO 3例,或囊性肿块合并炎性条索影4例(1例合并SBO)。此外,CT检查中发现的梅克尔憩室比锝高锝酸盐检查中多2.3倍。
目前,因腹痛行CT检查的儿童中,梅克尔憩室比锝高锝酸盐检查中更常见。CT上有三种表现类型:仅SBO、肠套叠或囊性炎性肿块。