scholarly journals Transverse testicular ectopia with fused vas deferens: A case series

2019 ◽  
Vol 24 (4) ◽  
pp. 288
Author(s):  
Sivasankar Jayakumar ◽  
Meena Agrawal
Keyword(s):  
Vas Deferens ◽  
Case Series ◽  
Transverse Testicular Ectopia ◽  
Testicular Ectopia

scholarly journals Transverse testicular ectopia with fused vas deferens

2021 ◽  
Vol 65 ◽  
pp. 101763
Author(s):  
Turyalai Hakimi ◽  
Maiwand Nijrabi ◽  
Khalid M-Qasem ◽  
Gh-Sakhi Hassani
Keyword(s):  
Vas Deferens ◽  
Transverse Testicular Ectopia ◽  
Testicular Ectopia

scholarly journals A Rare Variation of Transverse Testicular Ectopia (TTE) in a Young Adult as an Incidental Finding during Investigation for Testicular Pain

2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Chrysovalantis Gkekas ◽  
Evangelos N. Symeonidis ◽  
Ioannis Tsifountoudis ◽  
Christos Georgiadis ◽  
Vasileios Kalyvas ◽  
...  
Keyword(s):  
Vas Deferens ◽  
Sperm Count ◽  
Incidental Finding ◽  
Sperm Retrieval ◽  
Testicular Pain ◽  
Transverse Testicular Ectopia ◽  
Ectopic Testis ◽  
Close Proximity ◽  
Magnetic Resonance Imaging Mri ◽  
Testicular Ectopia

Transverse testicular ectopia (TTE) with fused vas deferens is an extremely rare clinical entity. Herein, we present a case of a 19-year-old patient with persistent left testicular pain lasting for a week. Clinical examination revealed an empty right hemiscrotum, a normal left-sided descended testis, and in close proximity a mass-like structure resembling testicular parenchyma. Laboratory tests were significant for elevated follicle-stimulating hormone (FSH), while sperm count revealed azoospermia. Ultrasound imaging (US) of the scrotum demonstrated the presence of both testes in the same left hemiscrotum with varicocele and no signs of inguinal hernia. Magnetic resonance imaging (MRI) of the penis and scrotum revealed TTE with a single, fused vas deferens, and hypoplastic seminal vesicles. Surgical intervention by means of microsurgical sperm retrieval and transseptal orchidopexy were considered but not performed, primarily owing to the patient’s unwillingness and to a lesser extent due to the restriction that the short and fused vas would pose in an attempt to transpose the ectopic testis. Therefore, an annual follow-up was recommended.

scholarly journals Transverse testicular ectopia in adults: A case series

2015 ◽  
Vol 6 (8) ◽  
pp. 465
Author(s):  
Divish Devendrakumar Saxena ◽  
Murtaza Akhtar ◽  
Mrinal Tandon
Keyword(s):  
Case Series ◽  
Transverse Testicular Ectopia ◽  
Testicular Ectopia

scholarly journals Transverse testicular ectopia with inguinal hernia in an adult—a case report

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Sudhakar Pitchumani ◽  
Elamparidhi Padmanaban ◽  
Yash Kumar Achantani ◽  
Rajasree Dhinadhayalan ◽  
Avinesh Varadane
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Inguinal Hernia ◽  
Seminal Vesicle ◽  
Vas Deferens ◽  
Wide Spectrum ◽  
Left Testis ◽  
Rare Congenital Anomaly ◽  
Transverse Testicular Ectopia ◽  
Testicular Ectopia

Abstract Background Transverse testicular ectopia (TTE) is a rare congenital anomaly in which both the testis are in the same hemiscrotum or one testis in the inguinal canal of the same side. It is usually associated with other anomalies such as inguinal hernia, persistent Mullerian duct syndrome (PMDS), true hermaphroditism, and pseudo-hermaphroditism. In this case report, we present a rare case of TTE in an adult patient with fused vas deferens, aplastic right seminal vesicle, and right side inguinal hernia. Case presentation A 33-year-old male came with complaint of severe pain in the scrotum for 2 days with a long-standing history of right inguinoscrotal swelling. Clinical examination revealed a right inguinoscrotal swelling in which right testis was not palpable separately and left testis was palpable at periphery of the left hemiscrotum. Ultrasound imaging and MRI of the scrotum revealed TTE with both testes in the left hemiscrotum, fused vas deferens, right aplastic and left hypoplastic seminal vesicle, right side patent process vaginalis with a non-obstructive, and non-strangulated inguinal hernia. Surgical intervention with transeptal orchidodpexy was advised but not performed due to the patient’s unwillingness. Hence, we recommended an annual follow-up for the same. Conclusion The present case report emphasizes that though TTE is a rare congenital anomaly, it should be considered as a differential diagnosis in patients with an absent testis and/or infertility, and a detailed imaging and biochemical investigation should be employed considering the wide spectrum of associated conditions.

Transverse testicular ectopia with supernumerary vas deferens and cyst of the ejaculatory duct

Urology ◽  
2001 ◽  
Vol 58 (3) ◽  
pp. 462 ◽  
Author(s):  
René Yiou ◽  
Thierry Lebret ◽  
Pierre Marie Lugagne ◽  
Vincent Molinié ◽  
Jean-Marie Hervé ◽  
...  
Keyword(s):  
Vas Deferens ◽  
Ejaculatory Duct ◽  
Transverse Testicular Ectopia ◽  
Testicular Ectopia

scholarly journals Transverse testicular ectopia with a blind ending vas deferens

2016 ◽  
Vol 32 (4) ◽  
pp. 317 ◽  
Author(s):  
AnjanKumar Dhua ◽  
Abhimanyu Varshney ◽  
Veereshwar Bhatnagar
Keyword(s):  
Vas Deferens ◽  
Transverse Testicular Ectopia ◽  
Blind Ending ◽  
Testicular Ectopia

Infantile scrotal hemangioma with transverse testicular ectopia

2021 ◽  
Author(s):  
Haley Sherburne ◽  
Remi Hamel ◽  
Daniel I. Schlessinger ◽  
Douglas E. Coplen ◽  
Susan Bayliss
Keyword(s):  
Transverse Testicular Ectopia ◽  
Testicular Ectopia
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