Gaspard Makambo Mohilo, Vincent Danvene Gonda, Maurice Masoda Nyamalyongo
{"title":"骶骨-尾骨畸胎瘤:关于在刚果民主共和国北乌班吉雅科马技术板非常有限的背景下报告的一个病例","authors":"Gaspard Makambo Mohilo, Vincent Danvene Gonda, Maurice Masoda Nyamalyongo","doi":"10.4236/OALIB.1107084","DOIUrl":null,"url":null,"abstract":"Sacrococcygeal teratoma is a very rare but often malignant congenital embryonic tumor. We report a case in an infant X aged 5 months, born eutocically in a pregnancy estimated at term. It was a third gesture, two parities and an abortion, a pregnancy punctuated by several episodes of illnesses not elucidated by her mother until childbirth. Due to the lack of a technical platform, the infant was not taken care of.","PeriodicalId":19593,"journal":{"name":"Open Access Library Journal","volume":"13 1","pages":"1-4"},"PeriodicalIF":0.0000,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sacro-Coccygian Teratoma: About a Case Reported in a Context with a very Limited Technical Plate in Yakoma, Nord-Ubangi, Democratic Republic of Congo\",\"authors\":\"Gaspard Makambo Mohilo, Vincent Danvene Gonda, Maurice Masoda Nyamalyongo\",\"doi\":\"10.4236/OALIB.1107084\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sacrococcygeal teratoma is a very rare but often malignant congenital embryonic tumor. We report a case in an infant X aged 5 months, born eutocically in a pregnancy estimated at term. It was a third gesture, two parities and an abortion, a pregnancy punctuated by several episodes of illnesses not elucidated by her mother until childbirth. Due to the lack of a technical platform, the infant was not taken care of.\",\"PeriodicalId\":19593,\"journal\":{\"name\":\"Open Access Library Journal\",\"volume\":\"13 1\",\"pages\":\"1-4\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Open Access Library Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4236/OALIB.1107084\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Access Library Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/OALIB.1107084","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Sacro-Coccygian Teratoma: About a Case Reported in a Context with a very Limited Technical Plate in Yakoma, Nord-Ubangi, Democratic Republic of Congo
Sacrococcygeal teratoma is a very rare but often malignant congenital embryonic tumor. We report a case in an infant X aged 5 months, born eutocically in a pregnancy estimated at term. It was a third gesture, two parities and an abortion, a pregnancy punctuated by several episodes of illnesses not elucidated by her mother until childbirth. Due to the lack of a technical platform, the infant was not taken care of.