{"title":"幼儿巨大囊性梅克尔憩室扭转:1例报告及简要文献回顾","authors":"Z. Zvizdic","doi":"10.5457/p2005-114.312","DOIUrl":null,"url":null,"abstract":"Objective: Herein we report an unusual case of torsed giant cystic Meckel’s diverticulum (MD) in a three-year-old boy, illustrating the rarity of this condition and briefly reviewing the literature on it. Case Report: A three-year-old boy who clinically presented with severe colicky abdominal pain and frequent vomiting. Abdominal ultrasonography showed a cystic lesion in the lower abdomen. Contrast-enhanced CT revealed a well-defined right upper quadrant cystic mass measuring ~5 × 4 cm. The cystic mass appeared to be arising from the small intestine. The radiological features were not suggestive of malignancy. An urgent laparotomy was performed. At operation, he was found to have an incomplete torsed giant cystic MD. Postoperative recovery was uneventful, and the patient was discharged on the sixth postoperative day. A regular, 3-year follow-up revealed no complications. Conclusion: A giant cystic Meckel’s diverticulum represents a rare cause of intra-abdominal/pelvic mass and should be considered in its differential diagnosis. Timely surgical intervention reduces morbidity and provides the best","PeriodicalId":36516,"journal":{"name":"Central European Journal of Paediatrics","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Twisting of a Giant Cystic Meckel’s Diverticulum in a Toddler: A Case Report and Brief Literature Review\",\"authors\":\"Z. Zvizdic\",\"doi\":\"10.5457/p2005-114.312\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: Herein we report an unusual case of torsed giant cystic Meckel’s diverticulum (MD) in a three-year-old boy, illustrating the rarity of this condition and briefly reviewing the literature on it. Case Report: A three-year-old boy who clinically presented with severe colicky abdominal pain and frequent vomiting. Abdominal ultrasonography showed a cystic lesion in the lower abdomen. Contrast-enhanced CT revealed a well-defined right upper quadrant cystic mass measuring ~5 × 4 cm. The cystic mass appeared to be arising from the small intestine. The radiological features were not suggestive of malignancy. An urgent laparotomy was performed. At operation, he was found to have an incomplete torsed giant cystic MD. Postoperative recovery was uneventful, and the patient was discharged on the sixth postoperative day. A regular, 3-year follow-up revealed no complications. Conclusion: A giant cystic Meckel’s diverticulum represents a rare cause of intra-abdominal/pelvic mass and should be considered in its differential diagnosis. Timely surgical intervention reduces morbidity and provides the best\",\"PeriodicalId\":36516,\"journal\":{\"name\":\"Central European Journal of Paediatrics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-03-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Central European Journal of Paediatrics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5457/p2005-114.312\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Central European Journal of Paediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5457/p2005-114.312","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Twisting of a Giant Cystic Meckel’s Diverticulum in a Toddler: A Case Report and Brief Literature Review
Objective: Herein we report an unusual case of torsed giant cystic Meckel’s diverticulum (MD) in a three-year-old boy, illustrating the rarity of this condition and briefly reviewing the literature on it. Case Report: A three-year-old boy who clinically presented with severe colicky abdominal pain and frequent vomiting. Abdominal ultrasonography showed a cystic lesion in the lower abdomen. Contrast-enhanced CT revealed a well-defined right upper quadrant cystic mass measuring ~5 × 4 cm. The cystic mass appeared to be arising from the small intestine. The radiological features were not suggestive of malignancy. An urgent laparotomy was performed. At operation, he was found to have an incomplete torsed giant cystic MD. Postoperative recovery was uneventful, and the patient was discharged on the sixth postoperative day. A regular, 3-year follow-up revealed no complications. Conclusion: A giant cystic Meckel’s diverticulum represents a rare cause of intra-abdominal/pelvic mass and should be considered in its differential diagnosis. Timely surgical intervention reduces morbidity and provides the best