RESUMEN
Anomalies in the müllerian ducts are congenital alterations with more prevalence than it is imagined, varying from 0.5 to 6.7% in the general population and up to 16.7% in women with recurrent miscarriage. The main findings are primary amenorrhea, dysmenorrhea, pelvic pain, endometriosis, sexual difficulties and low self-esteem. The major impact on the quality of life in women stricken by these problems justifies this study, whose objective is to analyze their most important aspects such as etiopathogeny, classification, diagnostic methods and proposed treatments. The research was performed on the Medline-PubMed database from 1904 to 2018. The American Fertility Society, European Society of Human Reproduction and Embryology, and the European Society of Gynaecological Endoscopy classify malformations as: Class 1/U5bC4V4: agenesis or hypoplasia of uterus and vagina; Class 1/U5aC4V4: cervical hypoplasia, associated with total or partial vaginal agenesis; Class 2/U4: unicornuate uterus; Class 3/U3bC2V1 or Class3/U3bC2V2: uterus didelphys; Class 4/U3C0: bicornuate uterus; Class 5/U2: septate uterus; Class 6: arcuate uterus; Class 7/U1: induced by diethylstilbestrol, represented by a T-shaped uterus; and V3: transverse vaginal septum. The diagnostic methods are the two-dimensional or three-dimensional ultrasound, MRI, hysterosalpingo-contrast-sonography, X-ray hysterosalpingography, hysteroscopy and laparoscopy. Some müllerian malformations are healed with surgery and/or self-dilatation. For vaginal agenesis, dilatation by Frank technique shows good results while malformations with obstruction of the menstrual flow need to be rapidly treated by surgery.
Asunto(s)
Dismenorrea/congénito , Endometriosis/congénito , Conductos Paramesonéfricos/anomalías , Dolor Pélvico/congénito , Anomalías Urogenitales/complicaciones , Útero/anomalías , Adulto , Anomalías Congénitas/diagnóstico , Anomalías Congénitas/etiología , Anomalías Congénitas/cirugía , Dismenorrea/diagnóstico , Dismenorrea/cirugía , Endometriosis/diagnóstico , Endometriosis/cirugía , Femenino , Humanos , Histerosalpingografía , Histeroscopía , Laparoscopía , Imagen por Resonancia Magnética , Dolor Pélvico/diagnóstico , Dolor Pélvico/cirugía , Embarazo , Disfunciones Sexuales Fisiológicas/diagnóstico , Disfunciones Sexuales Fisiológicas/etiología , Disfunciones Sexuales Fisiológicas/cirugía , Ultrasonografía , Anomalías Urogenitales/diagnóstico , Anomalías Urogenitales/cirugía , Útero/cirugía , Vagina/anomalías , Vagina/cirugíaRESUMEN
The fetal endometrium becomes responsive to steroid hormones around the fourth month of pregnancy starting with an oestrogenic phase, which is followed late in pregnancy by a secretory phase. Based on post-mortem studies, the endometrium at birth is secretory in only one-third of neonates and proliferative in the remaining cases. Decidual or menstrual changes are rare in fetal endometrium despite high circulating steroid hormone levels, which drop rapidly after birth. Hence, acquisition of progesterone responsiveness appears to be dependent on endometrial maturation and relative immaturity may persist in a majority of girls until the menarche and early adolescence. Two major reproductive disorders have been linked with either advanced or delayed endometrial maturation. First, early-onset endometriosis may be caused by menstruation-like bleeding in the neonate, leading to tubal reflux and ectopic implantation of endometrial stem/progenitor cells. Second, persistence of partial progesterone resistance in adolescent girls may compromise deep placentation and account for the increased risk of major obstetrical syndromes, including preeclampsia, fetal growth retardation and preterm birth. The concept of neonatal origins of common reproductive disorders poses important research challenges but also subsumes potential new preventative strategies.
Asunto(s)
Endometriosis/congénito , Endometrio/metabolismo , Desarrollo Fetal , Modelos Biológicos , Complicaciones del Embarazo/etiología , Progesterona/metabolismo , Adolescente , Medicina del Adolescente/tendencias , Animales , Investigación Biomédica/tendencias , Endometriosis/inmunología , Endometriosis/metabolismo , Endometriosis/fisiopatología , Endometrio/inmunología , Femenino , Enfermedades de los Genitales Femeninos/congénito , Enfermedades de los Genitales Femeninos/inmunología , Enfermedades de los Genitales Femeninos/metabolismo , Enfermedades de los Genitales Femeninos/fisiopatología , Humanos , Recién Nacido , Perinatología/tendencias , Placentación , Embarazo , Complicaciones del Embarazo/inmunología , Complicaciones del Embarazo/metabolismo , Complicaciones del Embarazo/prevención & control , Medicina Reproductiva/tendenciasAsunto(s)
Anomalías Múltiples/diagnóstico , Endometriosis/congénito , Obstrucción Intestinal/congénito , Complicaciones del Embarazo/fisiopatología , Resultado del Embarazo , Ultrasonografía Prenatal , Útero/anomalías , Vagina/anomalías , Anomalías Múltiples/diagnóstico por imagen , Endometriosis/complicaciones , Endometriosis/diagnóstico por imagen , Resultado Fatal , Femenino , Humanos , Recién Nacido , Obstrucción Intestinal/diagnóstico por imagen , Embarazo , Radiografía , SíndromeRESUMEN
Congenital cervico-vaginal atresia is a rare malformation; the presence of a functioning endometrium combined with this anomaly causes a retrograde menstruation and then a greater likelihood of endometriosis. Up to the present literature relates only thirteen cases in which congenital cervico-vaginal atresia was combined with a functioning endometrium. Primary amenorrhea and cyclic, cramping lower abdominal pain was the common symptoms of all the patients. In this work we report a new case of such pathology in a 23 old woman affected also by harmonic nanism. After the review of the literature the embryologic mechanisms involved in lower Mullerian tract malformations, the surgical treatment and the mechanism of formation of endometriosis in association with an outflow tract obstruction are discussed.