Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons
                                                   Official journal of the Indian Association of Pediatric Surgeons                           
Year : 2019  |  Volume : 24  |  Issue : 2  |  Page : 150--151

A rare case of transverse testicular ectopia


Mrinal Arora1, Jaswinder Kaur2, Rajeev Kulshreshtha1,  
1 Department of Pediatric Surgery, Sir Ganga Ram Hospital, New Delhi, India
2 Department of Pediatrics, Sir Ganga Ram Hospital, New Delhi, India

Correspondence Address:
Dr. Mrinal Arora
House No. 1057, Sector 16, Faridabad, Haryana
India




How to cite this article:
Arora M, Kaur J, Kulshreshtha R. A rare case of transverse testicular ectopia.J Indian Assoc Pediatr Surg 2019;24:150-151


How to cite this URL:
Arora M, Kaur J, Kulshreshtha R. A rare case of transverse testicular ectopia. J Indian Assoc Pediatr Surg [serial online] 2019 [cited 2019 Nov 11 ];24:150-151
Available from: http://www.jiaps.com/text.asp?2019/24/2/150/253331


Full Text



Sir,

Transverse testicular ectopia (TTE) or testicular pseudo-duplication/unilateral double testis/transverse aberrant testicular mal-descent is a rare anomaly in which both the testes descend through a single inguinal canal and lie in the same hemiscrotum. In the literature, less than 100 cases of TTE have been reported.[1] A 9-year-old boy was admitted with the chief complaint of bilateral empty scrotum since birth. He was operated elsewhere at the age of 2 years. As per parents, right-sided inguinal exploration was done, but testes could not be localized. Operative records were not available. When the child presented to us, he had an oblique surgical scar in the right inguinal region. There was no scar in the scrotal region. Scrotum was empty and poorly formed on both sides. Testis was palpable in the right inguinal region and no testis was palpable in the left scrotum or the left inguinal region. Ultrasound of the local region revealed the presence of both the testes in the right inguinal region and absence of any Mullerian structures. The child was posted for right inguinal exploration and bilateral orchidopexy. Right-sided inguinal exploration was done through the previous surgical scar. On exploration, both the testes were found in the right inguinal canal, attached to each other with separate cord structures [blood vessels and vas deferens, [Figure 1]. The testes along with the cord structures were separated. There were thick fibrotic attachments between the spermatic cords. The cords were separated up till the deep inguinal ring. The proximal testis was placed in the right hemiscrotum and the distal testis was placed in the left hemiscrotum, through an incision made in the scrotal septum. It was assured that both the testes reached the hemiscrotum without undue tension. Follow-up with ultrasound at 6 months postsurgery showed both the testes properly placed in the scrotum with good consistency and vascularity. TTE was first reported by von Lenhossek in 1886.[2] The various theories to suggest the etiopathogenesis are-dysfunction of the genitofemoral nerve, true crossover of the testis, both the testis arising from the same genital ridge or both lying in the same processus vaginalis before descent. Management is orchidopexy, either transseptal or extraperitoneal transposition orchidopexy. A search for Mullerian remnants and other anomalies should be done.[3] Laparoscopy better delineates the anatomy and enables us to see the crossing over of the spermatic cord towards the opposite side. It helps assess the testis and its side, vas, and vessels for length. The management depends upon the length of the vas and vessels. If length is severely inadequate, both the testes are fixed in the same hemiscrotum and if the length is adequate, then transseptal orchidopexy is recommended. In cases, where there is inadequate or just adequate length, transseptal contralateral orchidopexy can be done.[4]{Figure 1}

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient's parent has given his consent for his images and other clinical information to be reported in the journal. The patient's parent understands that his names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Fourcroy JL, Belman AB. Transverse testicular ectopia with persistent müllerian duct. Urology 1982;19:536-8.
2Von Lenhossek MN. Ectopia testis transversa. Anat Anz 1886;1:376-81.
3Pandey A, Gupta DK, Gangopadhyay AN, Sharma SP. Misdiagnosed transverse testicular ectopia: A rare entity. Hernia 2009;13:305-7.
4Raj V, Redkar R, Krishna S, Tewari S. Rare case of transverse testicular ectopia – Case report and review of literature. Int J Surg Case Rep 2017;41:407-10.