| Chen CD, Wu MY, Ho HN, Huang SC, Cheng CJ, Yang YS |
------>authors3_c=None ------>paper_class1=1 ------>Impact_Factor=None ------>paper_class3=2 ------>paper_class2=2 ------>vol=75 ------>confirm_bywho=tzengcr ------>insert_bywho=cjcheng ------>Jurnal_Rank=None ------>authors4_c=None ------>comm_author= ------>patent_EDate=None ------>authors5_c=None ------>publish_day=None ------>paper_class2Letter=None ------>page2=771 ------>medlineContent= ------>unit=000 ------>insert_date=20010330 ------>iam=5 ------>update_date= ------>author=??? ------>change_event=5 ------>ISSN=None ------>authors_c=None ------>score=175 ------>journal_name=Acta Obstetricia et Gynecologica Scandinavica ------>paper_name=Congenital atresia of the uterine cervix and vagina: report of case. ------>confirm_date=20030509 ------>tch_id=087010 ------>pmid=17465296 ------>page1=770 ------>fullAbstract=BACKGROUND: The existence of a longitudinal vaginal septum with double cervix communicating bilaterally with a nonseptate uterine body and normal adnexa is an unusual mullerian anomaly. CASE: A 43-year-old woman presented with menorrhagia and duplication of the cervix and vagina. Afibromatous uterus was suggested by clinical examination and confirmed by ultrasonography. The patient underwent total abdominal hysterectomy with bilateral salpingooophorectomy. The surgical specimen revealed a fibromatous uterus with double cervix communicating bilaterally with a nonseptate uterine body; both adnexa were normal. CONCLUSION: This rare mullerian anomaly is inconsistent with the classical embryologic theory of caudal to cranial mullerian development but supports the alternative embryologic hypothesis suggested by Muller et al, according to which fusion and absorption begin at the isthmus and proceed simultaneously in both the cranial and caudal directions. ------>tmu_sno=None ------>sno=3350 ------>authors2=None ------>authors3=None ------>authors4=None ------>authors5=None ------>authors6=None ------>authors6_c=None ------>authors=Chen CD, Wu MY, Ho HN, Huang SC, Cheng CJ, Yang YS ------>delete_flag=0 ------>SCI_JNo=None ------>authors2_c=None ------>publish_area=None ------>updateTitle=Double vagina and cervix communicating bilaterally with a single uterine cavity: report of a case with an unusual congenital uterine malformation. ------>language=2 ------>check_flag= ------>submit_date= ------>country=None ------>no=8 ------>patent_SDate=None ------>update_bywho= ------>publish_year=1996 ------>submit_flag= ------>publish_month=None |