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 ◽  
...  

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.

Author(s):  
Catarina Reis-de-Carvalho ◽  
Carolina Vaz-de-Macedo ◽  
Santiago Ortiz ◽  
Anabela Colaço ◽  
Carlos Calhaz-Jorge

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.


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

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

2007 ◽  
Vol 26 (3) ◽  
pp. 259-264 ◽  
Author(s):  
Olaf James Biedrzycki ◽  
Naveena Singh ◽  
Hani Habeeb ◽  
Neville Wathen ◽  
Asma Faruqi

2003 ◽  
Vol 90 (2) ◽  
pp. 478-481 ◽  
Author(s):  
Aycag Yorganci ◽  
Ebru Serinsoz ◽  
Arzu Ensari ◽  
Ayse Sertcelik ◽  
Firat Ortac

2021 ◽  
Vol 3 (5) ◽  
pp. 12-14
Author(s):  
M. Kaplanoglu

Imperforate hymen is a rare congenital female genital tract obstructive pathology. Although It is generally sporadic and isolated, very rare familial occurrence cases have been published in the literature. We present a rare case of the familial occurrence of IH and its surgical treatment. This case was admitted to our clinic with chronic pelvic pain, difficulty urination and pelvic mass. After the gynecologic examination and ultrasound view, the diagnosis of IH was made.  Her sister who two years older than she had been previously evaluated for amenorrhea and her sister had undergone surgical procedures for IH. Because of Hymen is an important symbol of virginity in family culture, hymen sparing surgery was performed. The familial occurrence of IH is a rare condition and very few reported cases in the literature. Hymenectomy can cause social retraction in cases therefore hymen sparing surgery is an important surgery, especially Muslim cultures.


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