scholarly journals Female Hypospadias and Congenital Uterine Müllerian Anomaly with Proved Fertility: A Rare Case Report

2011 ◽  
Vol 3 (3) ◽  
pp. 155-156
Author(s):  
Rekha Choudhary ◽  
Suniti Verma ◽  
Gautam Ram Choudhary
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Rare Case ◽  
Female Genital Tract ◽  
Urogenital Sinus ◽  
Developmental Relationship ◽  
Rare Case Report ◽  
Mullerian Anomaly ◽  
Primigravid Woman ◽  
Female Genital

ABSTRACT Congenital anomalies of the female genital tract result from müllerian duct anomalies and/or abnormalities of the urogenital sinus or cloaca. Due to the close developmental relationship between the genital and the urinary tracts, association of anomalies in both systems are common. This article reviews the appearance of developmental anomalies of the female urinary (hypospadias) and genital tracts and points out complication associated with bicornuate uterus. A 40-year-old primigravid woman conceived a pregnancy after 10 years of primary infertility. The prenatal course was uncomplicated. At 38 weeks’ gestation, she was successfully delivered by elective low transverse cesarean section.

scholarly journals Congenital absence of a part of the fallopian tube: a case report

2016 ◽  
Vol 6 (1) ◽  
pp. 320
Author(s):  
Mukta Agarwal ◽  
Hemali H. Sinha ◽  
. Anamika
Keyword(s):  
Case Report ◽  
Fallopian Tube ◽  
Genital Tract ◽  
Rare Case ◽  
Case Reports ◽  
Female Genital Tract ◽  
Fallopian Tubes ◽  
Rare Occurrence ◽  
Rare Case Report ◽  
Female Genital

Congenital malformations of female genital tract are frequently seen in Gynaecological clinics, incidence being upto 5-6% in cases of infertility. Most of these anomalies are related to uterus and vagina, abnormalities related to ovaries and fallopian tubes are of rare occurrence and the exact incidence of these anomalies are not known, only a few incidental case reports are available in literature. Here, we present a rare case report of absent mid- tubal segment of fallopian tube in a patient of infertility.

scholarly journals Cervical Mesonephric Adenocarcinoma: A Case Report of a Rare Gynecological Tumor from Embryological Remains of the Female Genital Tract

2021 ◽  
Author(s):  
Catarina Reis-de-Carvalho ◽  
Carolina Vaz-de-Macedo ◽  
Santiago Ortiz ◽  
Anabela Colaço ◽  
Carlos Calhaz-Jorge
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Female Genital Tract ◽  
Treatment Protocol ◽  
Gynecology And Obstetrics ◽  
Mesonephric Adenocarcinoma ◽  
Gynecological Tumor ◽  
Cervical Adenocarcinomas ◽  
Female Genital

Abstract Introduction Malignant mesonephric tumors are uncommon in the female genital tract, and they are usually located where embryonic remnants of Wolffian ducts are detected, such as the uterine cervix. The information about these tumors, their treatment protocol, and prognosis are scarce. Case report A 60-year-old woman with postmenopausal vaginal bleeding was initially diagnosed with endometrial carcinoma. After suspicion co-testing, the patient underwent a loop electrosurgical excision of the cervix and was eventually diagnosed with mesonephric adenocarcinoma. She was subjected to a radical hysterectomy, which revealed International Federation of Gynecology and Obstetrics (FIGO) IB1 stage, and adjuvant radiotherapy. The follow-up showed no evidence of recurrence after 60 months. Conclusion We present the case of a woman with cervical mesonephric adenocarcinoma. When compared with the literature, this case had the longest clinical follow-up without evidence of recurrence, which reinforces the concept that these tumors are associated with a favorable prognosis if managed according to the guidelines defined for the treatment of patients with cervical adenocarcinomas. Though a rare entity, it should be kept in mind as a differential diagnosis for other cervical cancers.

A patient from Zhejiang, China, with synchronous mucinous metaplasia and neoplasms of the female genital tract: A case report

2019 ◽  
Vol 45 (7) ◽  
pp. 1382-1385
Author(s):  
Jingjing Lu ◽  
Li Gao ◽  
Huimin Yu ◽  
Liang Xia ◽  
Xiuyu Guo ◽  
...  
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Female Genital Tract ◽  
Female Genital

Early triple malignancies of the female genital tract: A case report

1997 ◽  
Vol 2 (1) ◽  
pp. 51-54 ◽  
Author(s):  
Toshiko Jobo ◽  
Hiroaki Iwaya ◽  
Masahide Arai ◽  
Shoji Kamikatahira ◽  
Hiroyuki Kuramoto
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Female Genital Tract ◽  
Female Genital

scholarly journals Triple Synchronous Primary Neoplasms of the Cervix, Endometrium, and Ovary: A Rare Case Report and Summary of All the English PubMed-Indexed Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Ahmed Abu-Zaid ◽  
Mohannad Alsabban ◽  
Mohammed Abuzaid ◽  
Osama Alomar ◽  
Hany Salem ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Single Case ◽  
English Literature ◽  
Genital System ◽  
Summary Table ◽  
Female Genital System ◽  
Rare Case Report ◽  
Primary Neoplasms ◽  
Female Genital

The incidence rate of triple or more synchronous primary neoplasms of the female genital system is exceedingly uncommon. To the best of our knowledge, only 13 such cases have been reported in the PubMed-indexed English literature. Herein, we report a single case of triple synchronous primary neoplasms of the cervix, endometrium, and left ovary with three distinct histological patterns that were not reported previously. Moreover, we briefly present a summary table of all the English PubMed-indexed cases of triple or more synchronous primary neoplasms of the female genital system (n=13).

Solitary Fibrous Tumor of the Female Genital Tract A Case Report and Review of the Literature

2007 ◽  
Vol 26 (3) ◽  
pp. 259-264 ◽  
Author(s):  
Olaf James Biedrzycki ◽  
Naveena Singh ◽  
Hani Habeeb ◽  
Neville Wathen ◽  
Asma Faruqi
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Genital Tract ◽  
Female Genital Tract ◽  
Review Of The Literature ◽  
Fibrous Tumor ◽  
Female Genital

scholarly journals Neonatally Diagnosed Imperforate Hymen: Hymen Saving Surgery

2017 ◽  
Vol 24 (3) ◽  
pp. 55-59
Author(s):  
Maram A. Enani ◽  
Wejdan O. Ba-Amer ◽  
Alfaf S. Aljohani ◽  
Shahad A. Aljohani ◽  
Noor A. Aljohani ◽  
...  
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Genital Tract ◽  
Neonatal Period ◽  
Female Genital Tract ◽  
Late Diagnosis ◽  
Diagnosis And Treatment ◽  
Early Management ◽  
Imperforate Hymen ◽  
Female Genital

Imperforate hymen is the most common obstructive anomalies of the female genital tract. It is usually an isolated anomaly but can be rarely syndromic. It can be asymptomatic until puberty, but the diagnosis as early as neonatal period has been reported and as with our neonate with hematocolpos. The aim of this case report is to present the early diagnosis and treatment of a female neonate with imperforate hymen taking into consideration the religious and traditional value of preservation of virginity in our community, and to stress the importance of careful post birth examination of the neonate and early management to avoid complications of late diagnosis.

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