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2.
Ultrasound Obstet Gynecol ; 57(5): 821-828, 2021 05.
Artigo em Inglês | MEDLINE | ID: mdl-32770812

RESUMO

OBJECTIVE: To describe the clinical and ultrasound characteristics of accessory cavitated uterine malformations (ACUMs). METHODS: This was a single-center observational study of consecutive patients diagnosed with an ACUM, who had undergone an ultrasound examination by an experienced ultrasound examiner between January 2013 and May 2019, identified retrospectively from medical records. ACUM was diagnosed when a cavitated lesion with a myometrial mantle and echogenic contents was seen within the anterolateral wall of the myometrium beneath the insertion of the round ligament. In all women, presenting symptoms and clinical history were recorded along with detailed descriptions of the lesions and any concomitant pelvic abnormalities. RESULTS: Twenty patients diagnosed with an ACUM were identified. Median age was 29.2 (interquartile range, 25.0-35.8) years. None of the women was premenarchal or postmenopausal. All of the women reported painful periods or pelvic pain and none of them reported subfertility. Twelve of the ACUMs were in the right anterolateral myometrium and eight were in the left anterolateral myometrium. Both a myometrial mantle and a fluid-filled cavity were considered to be defining features on ultrasound. The fluid contained within the cavity was either echogenic with a ground-glass appearance or hyperechoic. All of the lesions were spherical in shape. The Doppler flow seen in the outer rim was not markedly different from that of the surrounding myometrium, and the content of the cavity was avascular on Doppler examination. The mean outer cavity diameter of the ACUMs was 22.8 (95% CI, 20.9-24.8) mm and the mean internal cavity diameter was 14.1 (95% CI, 12.2-16.1) mm. Four women opted for transvaginal ultrasound-guided alcohol sclerotherapy. Surgical excision was carried out in eight cases, and the diagnosis was confirmed on histopathological examination in all of them. CONCLUSIONS: ACUMs are a uterine abnormality with a distinct ultrasound appearance, which are associated with dysmenorrhea and chronic pelvic pain. Knowledge of their typical appearance on ultrasound could facilitate early detection and treatment. There are several treatment options for ACUM, ranging from simple analgesia to complete excision. Further prospective and longitudinal studies are required to study the prevalence and natural history of this condition. © 2020 International Society of Ultrasound in Obstetrics and Gynecology.


Assuntos
Ecocardiografia Doppler , Miométrio/anormalidades , Anormalidades Urogenitais/diagnóstico por imagem , Útero/anormalidades , Adulto , Dor Crônica/congênito , Dor Crônica/diagnóstico por imagem , Dismenorreia/congênito , Dismenorreia/diagnóstico por imagem , Feminino , Humanos , Miométrio/diagnóstico por imagem , Dor Pélvica/congênito , Dor Pélvica/diagnóstico por imagem , Estudos Retrospectivos , Ligamento Redondo do Útero/diagnóstico por imagem , Anormalidades Urogenitais/complicações , Útero/diagnóstico por imagem
3.
Taiwan J Obstet Gynecol ; 59(6): 948-951, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33218419

RESUMO

OBJECTIVE: Herlyn-Werner-Wünderlich (HWW) syndrome is a rare condition in which patients present with a palpable pelvic mass and pain caused by an obstructed hemivagina. Here we present a case of HWW syndrome characterized by prolonged menstrual bleeding. CASE REPORT: A 19-year-old nonsexually active unmarried women experienced irregular menstrual cycles and menorrhagia. The duration of menstrual bleeding was 10-14 days. She also suffered from mild dysmenorrhea since menarche at the age of 13. Transabdominal sonography revealed a double uterus and a heterogeneous myoma-mimicking mass over the left cervical region. The left kidney was absent. Magnetic resonance imaging revealed a double uterus, a double vagina with an unperforated left hemivagina, and ipsilateral renal agenesis. The patient underwent cervicovaginal orifice reconstruction surgery. CONCLUSION: Left hematocolpos compression, a partially obstructed right vaginal channel, and an orifice with local venous drainage abnormalities resulted in prolonged menstrual bleeding. In HWW syndrome, the occurrence of a pelvic mass and pain is common; however, prolonged menstrual bleeding is rare.


Assuntos
Anormalidades Múltiplas/diagnóstico , Menorragia/diagnóstico , Anormalidades Urogenitais/diagnóstico , Útero/anormalidades , Diagnóstico Diferencial , Feminino , Hematocolpia/congênito , Hematocolpia/diagnóstico , Humanos , Rim/anormalidades , Ilustração Médica , Menorragia/congênito , Dor Pélvica/congênito , Dor Pélvica/diagnóstico , Rim Único/congênito , Rim Único/diagnóstico , Síndrome , Anormalidades Urogenitais/complicações , Vagina/anormalidades , Adulto Jovem
4.
Taiwan J Obstet Gynecol ; 59(2): 183-188, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32127135

RESUMO

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.


Assuntos
Dismenorreia/congênito , Endometriose/congênito , Ductos Paramesonéfricos/anormalidades , Dor Pélvica/congênito , Anormalidades Urogenitais/complicações , Útero/anormalidades , Adulto , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/etiologia , Anormalidades Congênitas/cirurgia , Dismenorreia/diagnóstico , Dismenorreia/cirurgia , Endometriose/diagnóstico , Endometriose/cirurgia , Feminino , Humanos , Histerossalpingografia , Histeroscopia , Laparoscopia , Imageamento por Ressonância Magnética , Dor Pélvica/diagnóstico , Dor Pélvica/cirurgia , Gravidez , Disfunções Sexuais Fisiológicas/diagnóstico , Disfunções Sexuais Fisiológicas/etiologia , Disfunções Sexuais Fisiológicas/cirurgia , Ultrassonografia , Anormalidades Urogenitais/diagnóstico , Anormalidades Urogenitais/cirurgia , Útero/cirurgia , Vagina/anormalidades , Vagina/cirurgia
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