Cargando…
Testicular teratoma with nephroblastoma in an adult – case report and literature review
Testicular germ cell tumours are the most common malignancies in young men. Germ cell tumours can be classified as seminomas or non-seminomas, each with different clinical features and treatment approaches. Germ cell tumours are occasionally associated with somatic-type malignancy, particularly in m...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230240/ https://www.ncbi.nlm.nih.gov/pubmed/37266335 http://dx.doi.org/10.5114/wo.2023.127193 |
_version_ | 1785051485360357376 |
---|---|
author | Landin, Caroline Karlsson, Fredrik M. T. Småland, Mari Lorier Gabrych, Anna Kunc, Michał |
author_facet | Landin, Caroline Karlsson, Fredrik M. T. Småland, Mari Lorier Gabrych, Anna Kunc, Michał |
author_sort | Landin, Caroline |
collection | PubMed |
description | Testicular germ cell tumours are the most common malignancies in young men. Germ cell tumours can be classified as seminomas or non-seminomas, each with different clinical features and treatment approaches. Germ cell tumours are occasionally associated with somatic-type malignancy, particularly in metastatic lymph nodes after adjuvant chemotherapy. Adenocarcinomas and rhabdomyosarcoma are the most common malignancies in this setting. In this report, we present a unique case of a 37-year-old patient who presented with a testicular teratoma containing a nephroblastoma component. The tumour exhibited characteristic morphology that resembled foetal kidney and expressed nuclear WT-1 and PAX-8 on immunohistochemistry. Following surgery, the patient opted for active surveillance and remains disease-free. To date, only 7 cases of nephroblastoma in primary testicular teratoma have been reported. This case highlights the importance of considering this rare entity in the differential diagnosis of testicular teratomas and the need for careful pathological examination. |
format | Online Article Text |
id | pubmed-10230240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-102302402023-06-01 Testicular teratoma with nephroblastoma in an adult – case report and literature review Landin, Caroline Karlsson, Fredrik M. T. Småland, Mari Lorier Gabrych, Anna Kunc, Michał Contemp Oncol (Pozn) Case Report Testicular germ cell tumours are the most common malignancies in young men. Germ cell tumours can be classified as seminomas or non-seminomas, each with different clinical features and treatment approaches. Germ cell tumours are occasionally associated with somatic-type malignancy, particularly in metastatic lymph nodes after adjuvant chemotherapy. Adenocarcinomas and rhabdomyosarcoma are the most common malignancies in this setting. In this report, we present a unique case of a 37-year-old patient who presented with a testicular teratoma containing a nephroblastoma component. The tumour exhibited characteristic morphology that resembled foetal kidney and expressed nuclear WT-1 and PAX-8 on immunohistochemistry. Following surgery, the patient opted for active surveillance and remains disease-free. To date, only 7 cases of nephroblastoma in primary testicular teratoma have been reported. This case highlights the importance of considering this rare entity in the differential diagnosis of testicular teratomas and the need for careful pathological examination. Termedia Publishing House 2023-04-27 2023 /pmc/articles/PMC10230240/ /pubmed/37266335 http://dx.doi.org/10.5114/wo.2023.127193 Text en Copyright © 2023 Termedia https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ) |
spellingShingle | Case Report Landin, Caroline Karlsson, Fredrik M. T. Småland, Mari Lorier Gabrych, Anna Kunc, Michał Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title | Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title_full | Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title_fullStr | Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title_full_unstemmed | Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title_short | Testicular teratoma with nephroblastoma in an adult – case report and literature review |
title_sort | testicular teratoma with nephroblastoma in an adult – case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230240/ https://www.ncbi.nlm.nih.gov/pubmed/37266335 http://dx.doi.org/10.5114/wo.2023.127193 |
work_keys_str_mv | AT landincaroline testicularteratomawithnephroblastomainanadultcasereportandliteraturereview AT karlssonfredrikmt testicularteratomawithnephroblastomainanadultcasereportandliteraturereview AT smalandmarilorier testicularteratomawithnephroblastomainanadultcasereportandliteraturereview AT gabrychanna testicularteratomawithnephroblastomainanadultcasereportandliteraturereview AT kuncmichał testicularteratomawithnephroblastomainanadultcasereportandliteraturereview |