{"title":"Multiseptate胆囊。报告一个病例并复习文献。","authors":"K Okuda, M Nakajima, M Nakayama, F Nomura","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Multiseptate gallbladder is an extremely rare anomaly, the number of reported cases not having exceeded ten. In this 37-year-old man with a complaint of occasional nausea, vomiting and abdominal pain, intravenous cholecystography combined with tomography demonstrated a normal size gallbladder with many thin septa. The removed gallbladder had multiple intercommunicating locules divided by thin septa, looking like a honeycomb on the cut surface. The bile contained was dark brown in the neck and much lighter in color in the fundus, suggesting a disturbed bladder function. Histologically, some of the septa lacked the muscularis. He has been free of the previous complaints after surgery. Eight similar cases already documented are reviewed with a discussion on the embryogenetic aspect of this anomaly.</p>","PeriodicalId":7089,"journal":{"name":"Acta hepato-gastroenterologica","volume":"26 1","pages":"70-5"},"PeriodicalIF":0.0000,"publicationDate":"1979-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiseptate gallbladder. Report of a case with a review of literature.\",\"authors\":\"K Okuda, M Nakajima, M Nakayama, F Nomura\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Multiseptate gallbladder is an extremely rare anomaly, the number of reported cases not having exceeded ten. In this 37-year-old man with a complaint of occasional nausea, vomiting and abdominal pain, intravenous cholecystography combined with tomography demonstrated a normal size gallbladder with many thin septa. The removed gallbladder had multiple intercommunicating locules divided by thin septa, looking like a honeycomb on the cut surface. The bile contained was dark brown in the neck and much lighter in color in the fundus, suggesting a disturbed bladder function. Histologically, some of the septa lacked the muscularis. He has been free of the previous complaints after surgery. Eight similar cases already documented are reviewed with a discussion on the embryogenetic aspect of this anomaly.</p>\",\"PeriodicalId\":7089,\"journal\":{\"name\":\"Acta hepato-gastroenterologica\",\"volume\":\"26 1\",\"pages\":\"70-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1979-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta hepato-gastroenterologica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta hepato-gastroenterologica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Multiseptate gallbladder. Report of a case with a review of literature.
Multiseptate gallbladder is an extremely rare anomaly, the number of reported cases not having exceeded ten. In this 37-year-old man with a complaint of occasional nausea, vomiting and abdominal pain, intravenous cholecystography combined with tomography demonstrated a normal size gallbladder with many thin septa. The removed gallbladder had multiple intercommunicating locules divided by thin septa, looking like a honeycomb on the cut surface. The bile contained was dark brown in the neck and much lighter in color in the fundus, suggesting a disturbed bladder function. Histologically, some of the septa lacked the muscularis. He has been free of the previous complaints after surgery. Eight similar cases already documented are reviewed with a discussion on the embryogenetic aspect of this anomaly.