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A Rare Variation of Transverse Testicular Ectopia (TTE) in a Young Adult as an Incidental Finding during Investigation for Testicular Pain
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...
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Published in: | Case reports in urology 2018, Vol.2018 (2018), p.1-4 |
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creator | Papathanasiou, Michail Kalyvas, Vasileios Georgiadis, Christos Tsifountoudis, Ioannis Symeonidis, Evangelos N. Gkekas, Chrysovalantis Malioris, Apostolos |
description | 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. |
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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.</description><identifier>ISSN: 2090-696X</identifier><identifier>EISSN: 2090-6978</identifier><identifier>DOI: 10.1155/2018/6919387</identifier><identifier>PMID: 30643661</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Abdomen ; Case Report ; Case reports ; Follicle-stimulating hormone ; Hernia ; Hernias ; Pain ; Pediatrics ; Sperm ; Surgery ; Teenagers ; Ultrasound imaging ; Urology ; Young adults ; Youth</subject><ispartof>Case reports in urology, 2018, Vol.2018 (2018), p.1-4</ispartof><rights>Copyright © 2018 Chrysovalantis Gkekas et al.</rights><rights>COPYRIGHT 2018 John Wiley & Sons, Inc.</rights><rights>Copyright © 2018 Chrysovalantis Gkekas et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2018 Chrysovalantis Gkekas et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4167-46cd11b24d4f5aeb3b497a88a3aac127ebc8c678f1182f6eebe37a7e8b66de9e3</citedby><cites>FETCH-LOGICAL-c4167-46cd11b24d4f5aeb3b497a88a3aac127ebc8c678f1182f6eebe37a7e8b66de9e3</cites><orcidid>0000-0002-5414-0303 ; 0000-0002-6360-0762 ; 0000-0002-9792-5434 ; 0000-0001-6207-3844</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2161640629/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2161640629?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,25753,27923,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30643661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Goel, Apul</contributor><contributor>Apul Goel</contributor><creatorcontrib>Papathanasiou, Michail</creatorcontrib><creatorcontrib>Kalyvas, Vasileios</creatorcontrib><creatorcontrib>Georgiadis, Christos</creatorcontrib><creatorcontrib>Tsifountoudis, Ioannis</creatorcontrib><creatorcontrib>Symeonidis, Evangelos N.</creatorcontrib><creatorcontrib>Gkekas, Chrysovalantis</creatorcontrib><creatorcontrib>Malioris, Apostolos</creatorcontrib><title>A Rare Variation of Transverse Testicular Ectopia (TTE) in a Young Adult as an Incidental Finding during Investigation for Testicular Pain</title><title>Case reports in urology</title><addtitle>Case Rep Urol</addtitle><description>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. 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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.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30643661</pmid><doi>10.1155/2018/6919387</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-5414-0303</orcidid><orcidid>https://orcid.org/0000-0002-6360-0762</orcidid><orcidid>https://orcid.org/0000-0002-9792-5434</orcidid><orcidid>https://orcid.org/0000-0001-6207-3844</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Case Report Case reports Follicle-stimulating hormone Hernia Hernias Pain Pediatrics Sperm Surgery Teenagers Ultrasound imaging Urology Young adults Youth |
title | A Rare Variation of Transverse Testicular Ectopia (TTE) in a Young Adult as an Incidental Finding during Investigation for Testicular Pain |
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