Transvaginal ultrasound features of the residual cervix in pregnancy after radical trachelectomy

2020 ◽  
Vol 47 (2) ◽  
pp. 335-337
Author(s):  
Yoshifumi Kasuga ◽  
Kei Miyakoshi ◽  
Mamoru Tanaka
Ultrasound ◽  
2020 ◽  
Vol 28 (2) ◽  
pp. 82-90
Author(s):  
S Abdullahi Idle ◽  
K Hayes ◽  
JA Ross

Introduction Immature ovarian teratomas are rare but account for 10–20% of ovarian cancers in women under the age of 20 years. This study aimed to characterise immature ovarian teratomas using grey-scale and Doppler ultrasonography and review the literature to refine the diagnosis of immature ovarian teratomas. Methods Patients with a confirmed histological diagnosis of immature ovarian teratoma from years 2006–2018, who had undergone a transvaginal ultrasound at two large teaching hospitals, were identified. The imaging was retrieved from the centres clinical databases. Ultrasound scans were performed by experienced ultrasound examiners and described according to International Ovarian Tumour Analysis criteria. Results Eight patients were identified in total with a mean age of 26 years (range 13–35). Half of the patients had a past history of a mature ovarian teratoma (3 ipsilateral, 1 contralateral). The cysts were generally large (median 115 mm), fast growing unilateral lesions with a single, peripheral predominantly solid component arising from the cyst wall. The solid component was hyperechoic with multiple foci of fibrosis and numerous small cysts. The cystic component typically formed less than 75% of the lesion and the cyst fluid was of low-level echogenicity. Subjective assessment of vascularity of the solid part of the tumours varied between scores of 1 and 2. Tumour markers showed a raised serum a-fetoprotein level in 42% of these patients. Conclusion Although there were no ultrasound features that were pathognomonic of immature teratoma, the diagnosis should be suspected in a young woman with a large ovarian cyst with a fibrotic, microcystic solid component, particularly if she has a past history of a dermoid cyst.


Author(s):  
Michael S. Bold ◽  
James H. Boyum ◽  
Aaron M. Potretzke ◽  
Carl H. Rose ◽  
Thomas D. Atwell ◽  
...  

2021 ◽  
Vol 5 (4) ◽  
pp. 447-449
Author(s):  
Colin Jorgensen ◽  
Monika Lusiak

Introduction: Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications, both pregnancy and non-pregnancy related. Case Report: In this case, a pregnant 35-year-old female with vaginal bleeding was subsequently diagnosed with uterus didelphys by transvaginal ultrasound imaging. Conclusion: Despite its rarity, clinicians should be aware of MDAs and their associated complications with pregnancy.


2020 ◽  
Vol 47 (4) ◽  
pp. 655-657
Author(s):  
Yoshifumi Kasuga ◽  
Kei Miyakoshi ◽  
Toyohide Endo ◽  
Takashi Takeda ◽  
Masaru Nakamura ◽  
...  

2012 ◽  
Vol 140 (7-8) ◽  
pp. 511-514 ◽  
Author(s):  
Radmila Sparic ◽  
Snezana Buzadzic ◽  
Rajka Argirovic ◽  
Danijela Bratic ◽  
Darko Plecas

Introduction. Heterotopic pregnancy is a life-threatening complication of pregnancy defined as coexistent intrauterine and ectopic gestation. Its diagnosis is frequently overlooked and delayed. Case Outline. A 28-year-old woman experienced acute abdominal pain in pregnancy achieved by in vitro fertilization. Since all previous checkups indicated a normal course of pregnancy, the ectopic pregnancy was not suspected on admission. However, due to persistent hypotension, this diagnosis was also considered. Transvaginal ultrasound performed by an experienced obstetrician revealed an adnexal mass highly indicative of ectopic pregnancy. No fetal heart beats were visualized and the diagnosis of a missed abortion was made. A prompt laparotomy revealed a ruptured right ampullary pregnancy, and salpingectomy was performed. Conclusion. Although rare, heterotopic pregnancy should be considered in the differential diagnosis of abdominal pain in pregnancy. Every physician treating women of reproductive age should bear in mind the possibility of heterotopic pregnancy not only in patients with predisposing risk factors but also in those without them.


Sign in / Sign up

Export Citation Format

Share Document