A. Gautam, Bijay Subedi, M. Dhital, J. Awasthi, S. Adhikari, Purushottam Adhikari
{"title":"结石引起的右侧两个独立骨盆系统伴双输尿管的肾盂肾盂积水梗阻性综合征:罕见的临床病例。","authors":"A. Gautam, Bijay Subedi, M. Dhital, J. Awasthi, S. Adhikari, Purushottam Adhikari","doi":"10.55530/ijmbiosnepal.v2i2.24","DOIUrl":null,"url":null,"abstract":"Hydroureteronephrosis is a clinical condition where the dilatation of renal calyces and ureter occur jointly due to obstruction. When two ureters arise from single kidney the situation is known as bifid ureter which may be complete orincomplete. The present study examines a congenital anomaly of bifid ureter and rare clinical presentation of calculusinduced obstructive hydroureternephrosis in a adult male aged 38 by past 48 hours. The common symptoms of thiscondition were extreme intolerable pain in the abdomen, flank pain moderate to severe radiate to loin to groin,vomiting/nausea and haematuria. Diagnosis was done by injection of intravenous dye and computed tomographyintravenous pyleogram was performed along with lab findings. In this case we found two incomplete ureters i.e. bifidnature arising from right kidney that unite as a single ureter before emptying into the urinary bladder. There was presence of single large calculus measuring approximately 8.6*8mm right at the junction of bifid ureter at the level of L3 vertebra inducing hydroureteronephrosis. Similarly marked upstream dilation of upper right ureter was found. The anomaly of bifid ureter occurs due to the untimely division of ureteric diverticulum. Unless some complication of ureter occurs, the duplication does not expose itself. Acute obstruction of ureter does not cause any significant alternation in renal function. Though the whole clinical presentation is rare itself, it further needs follow ups to avoid re-occurrence.","PeriodicalId":359742,"journal":{"name":"International Journal of Medicine and Biomedical Sciences","volume":"22 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Calculus Induced Hydroureteronephrosis Obstructive Syndrome in a Patient with Two Separate Pelvicalcyeal System in Right Side with Bifid Ureter: A Rare Clinical Entity.\",\"authors\":\"A. Gautam, Bijay Subedi, M. Dhital, J. Awasthi, S. Adhikari, Purushottam Adhikari\",\"doi\":\"10.55530/ijmbiosnepal.v2i2.24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hydroureteronephrosis is a clinical condition where the dilatation of renal calyces and ureter occur jointly due to obstruction. When two ureters arise from single kidney the situation is known as bifid ureter which may be complete orincomplete. The present study examines a congenital anomaly of bifid ureter and rare clinical presentation of calculusinduced obstructive hydroureternephrosis in a adult male aged 38 by past 48 hours. The common symptoms of thiscondition were extreme intolerable pain in the abdomen, flank pain moderate to severe radiate to loin to groin,vomiting/nausea and haematuria. Diagnosis was done by injection of intravenous dye and computed tomographyintravenous pyleogram was performed along with lab findings. In this case we found two incomplete ureters i.e. bifidnature arising from right kidney that unite as a single ureter before emptying into the urinary bladder. There was presence of single large calculus measuring approximately 8.6*8mm right at the junction of bifid ureter at the level of L3 vertebra inducing hydroureteronephrosis. Similarly marked upstream dilation of upper right ureter was found. The anomaly of bifid ureter occurs due to the untimely division of ureteric diverticulum. Unless some complication of ureter occurs, the duplication does not expose itself. Acute obstruction of ureter does not cause any significant alternation in renal function. Though the whole clinical presentation is rare itself, it further needs follow ups to avoid re-occurrence.\",\"PeriodicalId\":359742,\"journal\":{\"name\":\"International Journal of Medicine and Biomedical Sciences\",\"volume\":\"22 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Medicine and Biomedical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55530/ijmbiosnepal.v2i2.24\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Medicine and Biomedical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55530/ijmbiosnepal.v2i2.24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Calculus Induced Hydroureteronephrosis Obstructive Syndrome in a Patient with Two Separate Pelvicalcyeal System in Right Side with Bifid Ureter: A Rare Clinical Entity.
Hydroureteronephrosis is a clinical condition where the dilatation of renal calyces and ureter occur jointly due to obstruction. When two ureters arise from single kidney the situation is known as bifid ureter which may be complete orincomplete. The present study examines a congenital anomaly of bifid ureter and rare clinical presentation of calculusinduced obstructive hydroureternephrosis in a adult male aged 38 by past 48 hours. The common symptoms of thiscondition were extreme intolerable pain in the abdomen, flank pain moderate to severe radiate to loin to groin,vomiting/nausea and haematuria. Diagnosis was done by injection of intravenous dye and computed tomographyintravenous pyleogram was performed along with lab findings. In this case we found two incomplete ureters i.e. bifidnature arising from right kidney that unite as a single ureter before emptying into the urinary bladder. There was presence of single large calculus measuring approximately 8.6*8mm right at the junction of bifid ureter at the level of L3 vertebra inducing hydroureteronephrosis. Similarly marked upstream dilation of upper right ureter was found. The anomaly of bifid ureter occurs due to the untimely division of ureteric diverticulum. Unless some complication of ureter occurs, the duplication does not expose itself. Acute obstruction of ureter does not cause any significant alternation in renal function. Though the whole clinical presentation is rare itself, it further needs follow ups to avoid re-occurrence.