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Splenogonadal fusion: A rare case report and literature review

Splenogonadal fusion is a rare benign congenital anomaly with few cases described in the literature. It is 16 times more common in males than in females. A 22 year-old healthy male with cryptorchidism presented with preoperative imaging strongly suggestive of malignancy. Histopathology after left or...

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Autores principales: Alsunbul, Abdulrahman, Alsuhaibani, Shaheed, Al Ali, Hamed, Alhussain, Turki, Aldawsari, Nasser, Alhathal, Naif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573839/
https://www.ncbi.nlm.nih.gov/pubmed/33102010
http://dx.doi.org/10.1016/j.eucr.2020.101307
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author Alsunbul, Abdulrahman
Alsuhaibani, Shaheed
Al Ali, Hamed
Alhussain, Turki
Aldawsari, Nasser
Alhathal, Naif
author_facet Alsunbul, Abdulrahman
Alsuhaibani, Shaheed
Al Ali, Hamed
Alhussain, Turki
Aldawsari, Nasser
Alhathal, Naif
author_sort Alsunbul, Abdulrahman
collection PubMed
description Splenogonadal fusion is a rare benign congenital anomaly with few cases described in the literature. It is 16 times more common in males than in females. A 22 year-old healthy male with cryptorchidism presented with preoperative imaging strongly suggestive of malignancy. Histopathology after left orchiectomy showed mixed splenic and testicular tissue with no sign of malignancy. Splenogonadal fusion is rarely diagnosed preoperatively. It should be included in differential diagnoses in patients presenting with a testicular or abdominal mass. Greater recognition of this rare anomaly may facilitate testis sparing surgery in future cases.
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spelling pubmed-75738392020-10-23 Splenogonadal fusion: A rare case report and literature review Alsunbul, Abdulrahman Alsuhaibani, Shaheed Al Ali, Hamed Alhussain, Turki Aldawsari, Nasser Alhathal, Naif Urol Case Rep Andrology and Fertility Splenogonadal fusion is a rare benign congenital anomaly with few cases described in the literature. It is 16 times more common in males than in females. A 22 year-old healthy male with cryptorchidism presented with preoperative imaging strongly suggestive of malignancy. Histopathology after left orchiectomy showed mixed splenic and testicular tissue with no sign of malignancy. Splenogonadal fusion is rarely diagnosed preoperatively. It should be included in differential diagnoses in patients presenting with a testicular or abdominal mass. Greater recognition of this rare anomaly may facilitate testis sparing surgery in future cases. Elsevier 2020-06-17 /pmc/articles/PMC7573839/ /pubmed/33102010 http://dx.doi.org/10.1016/j.eucr.2020.101307 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Andrology and Fertility
Alsunbul, Abdulrahman
Alsuhaibani, Shaheed
Al Ali, Hamed
Alhussain, Turki
Aldawsari, Nasser
Alhathal, Naif
Splenogonadal fusion: A rare case report and literature review
title Splenogonadal fusion: A rare case report and literature review
title_full Splenogonadal fusion: A rare case report and literature review
title_fullStr Splenogonadal fusion: A rare case report and literature review
title_full_unstemmed Splenogonadal fusion: A rare case report and literature review
title_short Splenogonadal fusion: A rare case report and literature review
title_sort splenogonadal fusion: a rare case report and literature review
topic Andrology and Fertility
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573839/
https://www.ncbi.nlm.nih.gov/pubmed/33102010
http://dx.doi.org/10.1016/j.eucr.2020.101307
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