{"title":"在贝宁Menontin医院先天性巨乳症:一个病例报告和文献回顾","authors":"Agounkpe Michel, Behanzin Ulrich, Mkoh Anne, Valimungighe M. Moïse, Avakoudjo D.G Josué","doi":"10.31254/jmr.2023.9405","DOIUrl":null,"url":null,"abstract":"Background: Congenital megacalice of Puigvert is a rare congenital anomaly characterized by non-obstructive dilatation of the renal calyces with normal pelvis, ureter and bladder. Clinic Observation: We report the case of a left congenital megacaliceus without lithiasis or obstruction in a 36-year-old female patient discovered on uroscanner indicated for chronic abdominal pain. Conclusion: Congenital megacalice is a rare pathology, and only clinical and biological monitoring remains the basis of its management.","PeriodicalId":50132,"journal":{"name":"Journal of Medical Research","volume":"51 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Congenital megacalice at Menontin Hospital in Benin: A case report and review of the literature\",\"authors\":\"Agounkpe Michel, Behanzin Ulrich, Mkoh Anne, Valimungighe M. Moïse, Avakoudjo D.G Josué\",\"doi\":\"10.31254/jmr.2023.9405\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Congenital megacalice of Puigvert is a rare congenital anomaly characterized by non-obstructive dilatation of the renal calyces with normal pelvis, ureter and bladder. Clinic Observation: We report the case of a left congenital megacaliceus without lithiasis or obstruction in a 36-year-old female patient discovered on uroscanner indicated for chronic abdominal pain. Conclusion: Congenital megacalice is a rare pathology, and only clinical and biological monitoring remains the basis of its management.\",\"PeriodicalId\":50132,\"journal\":{\"name\":\"Journal of Medical Research\",\"volume\":\"51 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31254/jmr.2023.9405\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31254/jmr.2023.9405","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Congenital megacalice at Menontin Hospital in Benin: A case report and review of the literature
Background: Congenital megacalice of Puigvert is a rare congenital anomaly characterized by non-obstructive dilatation of the renal calyces with normal pelvis, ureter and bladder. Clinic Observation: We report the case of a left congenital megacaliceus without lithiasis or obstruction in a 36-year-old female patient discovered on uroscanner indicated for chronic abdominal pain. Conclusion: Congenital megacalice is a rare pathology, and only clinical and biological monitoring remains the basis of its management.
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