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A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy

Splenogonadal fusion (SGF) is a rare benign malformation in which spleen is aberrantly attached to the gonads or mesonephric derivatives. This entity often presents with scrotal mass, inguinal hernia, or cryptorchidism. Herein, we report our experience with a boy who presented with a scrotal enlarge...

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Autores principales: Shakeri, Aria, Shakeri, Arash, Rasolmali, Reza, Shakeri, Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194785/
https://www.ncbi.nlm.nih.gov/pubmed/30386095
http://dx.doi.org/10.4103/UA.UA_194_17
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author Shakeri, Aria
Shakeri, Arash
Rasolmali, Reza
Shakeri, Saeed
author_facet Shakeri, Aria
Shakeri, Arash
Rasolmali, Reza
Shakeri, Saeed
author_sort Shakeri, Aria
collection PubMed
description Splenogonadal fusion (SGF) is a rare benign malformation in which spleen is aberrantly attached to the gonads or mesonephric derivatives. This entity often presents with scrotal mass, inguinal hernia, or cryptorchidism. Herein, we report our experience with a boy who presented with a scrotal enlargement which later turned out to be SGF. Moreover, an accessory spleen was unexpectedly found in the left inguinal canal. To the best of our knowledge, this is the first report of SGF and accessory spleen in the literature. Although rare, SGF should be included in the complete differential diagnosis list of scrotal masses, especially in children. The use of frozen section pathology if available would aid the surgeon in avoiding unnecessary orchiectomy in small testicular masses of benign origin.
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spelling pubmed-61947852018-10-31 A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy Shakeri, Aria Shakeri, Arash Rasolmali, Reza Shakeri, Saeed Urol Ann Case Report Splenogonadal fusion (SGF) is a rare benign malformation in which spleen is aberrantly attached to the gonads or mesonephric derivatives. This entity often presents with scrotal mass, inguinal hernia, or cryptorchidism. Herein, we report our experience with a boy who presented with a scrotal enlargement which later turned out to be SGF. Moreover, an accessory spleen was unexpectedly found in the left inguinal canal. To the best of our knowledge, this is the first report of SGF and accessory spleen in the literature. Although rare, SGF should be included in the complete differential diagnosis list of scrotal masses, especially in children. The use of frozen section pathology if available would aid the surgeon in avoiding unnecessary orchiectomy in small testicular masses of benign origin. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6194785/ /pubmed/30386095 http://dx.doi.org/10.4103/UA.UA_194_17 Text en Copyright: © 2018 Urology Annals http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Shakeri, Aria
Shakeri, Arash
Rasolmali, Reza
Shakeri, Saeed
A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title_full A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title_fullStr A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title_full_unstemmed A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title_short A case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
title_sort case of splenogonadal fusion accompanied by accessory spleen in a 4-year-old boy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194785/
https://www.ncbi.nlm.nih.gov/pubmed/30386095
http://dx.doi.org/10.4103/UA.UA_194_17
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