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Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report

Paratesticular tumours are pathologically rare. The vast majority are benign in nature with adenomatoid tumours representing the most common pathological entity. We present the case of a 32-year-old man, from the Indian subcontinent, who presented with a painful scrotal swelling sustained after trau...

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Detalles Bibliográficos
Autores principales: Gupta, A., Livingston, M., Singh, R., Tansey, D., Solomon, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638494/
https://www.ncbi.nlm.nih.gov/pubmed/23691428
http://dx.doi.org/10.1155/2013/937689
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author Gupta, A.
Livingston, M.
Singh, R.
Tansey, D.
Solomon, L.
author_facet Gupta, A.
Livingston, M.
Singh, R.
Tansey, D.
Solomon, L.
author_sort Gupta, A.
collection PubMed
description Paratesticular tumours are pathologically rare. The vast majority are benign in nature with adenomatoid tumours representing the most common pathological entity. We present the case of a 32-year-old man, from the Indian subcontinent, who presented with a painful scrotal swelling sustained after trauma. The history suggested that the scrotal mass had been present for approximately 12 months, and a preliminary diagnosis of a haemorrhagic cyst caused by trauma was made. Initial management included scrotal support, analgesia, and a follow-up magnetic resonance imaging (MRI) scan. Subsequent imaging and then further histological analysis confirmed a partly necrotic/infarcted adenomatoid tumour of the right epididymis. After scrotal exploration and epididymectomy, the patient made a complete recovery, and, with the histological diagnosis, he was discharged with no further followup. The case is presented as a learning point in the identification and management of such pathologies.
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spelling pubmed-36384942013-05-20 Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report Gupta, A. Livingston, M. Singh, R. Tansey, D. Solomon, L. Case Rep Urol Case Report Paratesticular tumours are pathologically rare. The vast majority are benign in nature with adenomatoid tumours representing the most common pathological entity. We present the case of a 32-year-old man, from the Indian subcontinent, who presented with a painful scrotal swelling sustained after trauma. The history suggested that the scrotal mass had been present for approximately 12 months, and a preliminary diagnosis of a haemorrhagic cyst caused by trauma was made. Initial management included scrotal support, analgesia, and a follow-up magnetic resonance imaging (MRI) scan. Subsequent imaging and then further histological analysis confirmed a partly necrotic/infarcted adenomatoid tumour of the right epididymis. After scrotal exploration and epididymectomy, the patient made a complete recovery, and, with the histological diagnosis, he was discharged with no further followup. The case is presented as a learning point in the identification and management of such pathologies. Hindawi Publishing Corporation 2013 2013-04-03 /pmc/articles/PMC3638494/ /pubmed/23691428 http://dx.doi.org/10.1155/2013/937689 Text en Copyright © 2013 A. Gupta et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gupta, A.
Livingston, M.
Singh, R.
Tansey, D.
Solomon, L.
Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title_full Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title_fullStr Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title_full_unstemmed Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title_short Infarcted Adenomatoid Tumour of Epididymis: A Rare Case Report
title_sort infarcted adenomatoid tumour of epididymis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638494/
https://www.ncbi.nlm.nih.gov/pubmed/23691428
http://dx.doi.org/10.1155/2013/937689
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