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Normal And Abnormal Development Of Female Genital Tract. Dr Khalid Sait FRCSC A. Prof Gynecologist Oncologist. Embryology. Baby sex established at the time of fertilization ( sperm meet ovum )
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Normal And Abnormal Development Of Female Genital Tract Dr Khalid Sait FRCSC A. Prof Gynecologist Oncologist
Embryology • Baby sex established at the time of fertilization ( sperm meet ovum ) • sperm 46 xy ovum 46 xx (23x + 23 y) (23 x + 23 x) Boy Girl
Genetic sex XX / XY Gonadal sex Testes / Ovaries Hormones External genitalia Internal genitalia
Embryology • Gonads appear as genital ridges by proliferation of coalemic epithelium(mesoderm) • Primordal germ cell appear in the endodermal cell in the wall of yolk sac , migrate along the mesentery of hindgut and invade the genital ridges • At 7 weeks the gonads of embryo: indistinguishable male and female ( indifferent gonad) • At 8 weeks if xx ----- Ovary xy------- Testis
EmbryologyOvary • Gonadal ovary : medullary cord degenerate and cortical cord develop • Germ cells ----oogonia • 11-12 w : onset of oogenesis • 20 w : 7 million germ cells in each ovary • Birth : 2 millions • Puberty : 40,000 primary oocytes remaining in the ovaries. Only 400 ------------- secondary oocytes and extended at ovulation once every month during menst. Cycle. • Descend of ovary is not an active migration, but result of rapid growth of body and failure of gubernaculum to elongatee ( that why its maintain blood supply from the aorta
Congenital Uterine Anomaly • Precise incidence is unknown (range from 1-2 %) • Clinical presentation: 1 Usually asymptomatic 2 Menstrual disorder 3Dysmenorrhea 4Recurrent abortion ( decrease intrauterine volume and vascularity, increase uterine irritability and cervical incompetance ) 5 Premature labor 6 Abnormal presentation 7 Primary infertility
Congenital Uterine Anomaly • Diagnosis: History Pelvic exam Hysterosalpingography U/S MRI Laproscopy Hysteroscopy IVP or U/S (Exclude Renal anomaly )
Congenital Uterine Anomaly • Treatment: 1-Double uterus (didelphic uterus): no need to treat. 2-Bicornate ut. --------- Strassmann procedure ( if indicated ) 3-Ut. Septum --------- (BCP for dysmenorrhea ), Tompkins metroplasty or Hysteroscopic resection of septum ) 4-Unicornate ut. -------- Surgery indicated if there is blind horn which cause symptom----- surgical resection of blind horn.
Mullerian Agenesis • Mayer Custer Hauser Rokitansky Syndrome • 1: 4000 • Abscent upper vagina, cervix and uterus and tubes • Normal ovaries and vulva • Associated with spine and renal anomaly • Treatment: McIndoe procedure Self dilatation of vagina
Vaginal Agenesis • 1: 5000 • Normal Vulva • Ass. With spine, renal and middle ear anomaly • Treatment: Karyotype, U/S - MRI ( only 5 % will have normal functioning uterus) Once patient sexually active 1-Gradual vaginal dilatation against vaginal dimple (daily for 20-30 mint for few month with gradual dilators size. 2-William procedure 3-Wharton and Macindo procedure
Transverse Vaginal Septum • Mid vagina usually • May be partial or complete • Presentation: Primary amenorrhea Dysparonia • Treatment:Surgical resection
Imperforated Hymen • Presentation: Primary Amenorrhea Pelvic mass • Treatment:Cuciate incision at hymen • Follow upEndometrosis Vaginal adenosis