Abnormal urethral pathways in a child presenting with diphallia
Diphallia is an extremely rare embryological anomaly, occurring once in 5–6 million births. Here we discuss a neonate who was referred for surgical consultation of diphallia, in which examination revealed a dominant right phallus and apparently shorter left phallus. MRI and retrograde urethrogram re...
Main Authors: | , , |
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Format: | Article |
Language: | English |
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Elsevier
2021-03-01
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Series: | Journal of Pediatric Surgery Case Reports |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2213576621000245 |
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author | Dylan John Kendrick Lucy Erin Goddard Roy Mark Kimble |
author_facet | Dylan John Kendrick Lucy Erin Goddard Roy Mark Kimble |
author_sort | Dylan John Kendrick |
collection | DOAJ |
description | Diphallia is an extremely rare embryological anomaly, occurring once in 5–6 million births. Here we discuss a neonate who was referred for surgical consultation of diphallia, in which examination revealed a dominant right phallus and apparently shorter left phallus. MRI and retrograde urethrogram revealed a unique pathway of the right urethra and a stenosed, but otherwise normal left urethra. The decision was made to excise the right phallus and associated urethra due to the correct anatomy of the left phallus and corresponding urethra. |
first_indexed | 2024-12-20T08:40:46Z |
format | Article |
id | doaj.art-811ddc8585694a51bb37964607739b9f |
institution | Directory Open Access Journal |
issn | 2213-5766 |
language | English |
last_indexed | 2024-12-20T08:40:46Z |
publishDate | 2021-03-01 |
publisher | Elsevier |
record_format | Article |
series | Journal of Pediatric Surgery Case Reports |
spelling | doaj.art-811ddc8585694a51bb37964607739b9f2022-12-21T19:46:24ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662021-03-0166101802Abnormal urethral pathways in a child presenting with diphalliaDylan John Kendrick0Lucy Erin Goddard1Roy Mark Kimble2University of Queensland, School of Medicine, Australia; Corresponding author.Queensland Children's Hospital, 501 Stanley St., South Brisbane, Queensland, 4101, AustraliaUniversity of Queensland, School of Medicine, Australia; Queensland Children's Hospital, 501 Stanley St., South Brisbane, Queensland, 4101, Australia; Queensland University of Technology, School of Health Sciences, AustraliaDiphallia is an extremely rare embryological anomaly, occurring once in 5–6 million births. Here we discuss a neonate who was referred for surgical consultation of diphallia, in which examination revealed a dominant right phallus and apparently shorter left phallus. MRI and retrograde urethrogram revealed a unique pathway of the right urethra and a stenosed, but otherwise normal left urethra. The decision was made to excise the right phallus and associated urethra due to the correct anatomy of the left phallus and corresponding urethra.http://www.sciencedirect.com/science/article/pii/S2213576621000245DiphalliaDuplicate penisUrethral duplicationCongenital anomaly |
spellingShingle | Dylan John Kendrick Lucy Erin Goddard Roy Mark Kimble Abnormal urethral pathways in a child presenting with diphallia Journal of Pediatric Surgery Case Reports Diphallia Duplicate penis Urethral duplication Congenital anomaly |
title | Abnormal urethral pathways in a child presenting with diphallia |
title_full | Abnormal urethral pathways in a child presenting with diphallia |
title_fullStr | Abnormal urethral pathways in a child presenting with diphallia |
title_full_unstemmed | Abnormal urethral pathways in a child presenting with diphallia |
title_short | Abnormal urethral pathways in a child presenting with diphallia |
title_sort | abnormal urethral pathways in a child presenting with diphallia |
topic | Diphallia Duplicate penis Urethral duplication Congenital anomaly |
url | http://www.sciencedirect.com/science/article/pii/S2213576621000245 |
work_keys_str_mv | AT dylanjohnkendrick abnormalurethralpathwaysinachildpresentingwithdiphallia AT lucyeringoddard abnormalurethralpathwaysinachildpresentingwithdiphallia AT roymarkkimble abnormalurethralpathwaysinachildpresentingwithdiphallia |