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Paratesticular Serous Borderline Tumor in a Pediatric Patient

Tumors of the paratesticular region are generally tumors of slow growth, with little symptomatology and, in most cases, benign in nature; in this area, a borderline serous tumor may arise hypothetically from Müllerian metaplasia of the tunica vaginalis, which is histologically identical to its ovari...

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Autores principales: Meza, Itzel Araceli Ortiz, Camacho, Marco Antonio Ponce, Márquez, Rodolfo Franco, Morquecho, Mauricio Delgado, Guajardo, Raquel Garza, Quintana, Oralia Barboza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591986/
https://www.ncbi.nlm.nih.gov/pubmed/33133717
http://dx.doi.org/10.1155/2020/8789143
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author Meza, Itzel Araceli Ortiz
Camacho, Marco Antonio Ponce
Márquez, Rodolfo Franco
Morquecho, Mauricio Delgado
Guajardo, Raquel Garza
Quintana, Oralia Barboza
author_facet Meza, Itzel Araceli Ortiz
Camacho, Marco Antonio Ponce
Márquez, Rodolfo Franco
Morquecho, Mauricio Delgado
Guajardo, Raquel Garza
Quintana, Oralia Barboza
author_sort Meza, Itzel Araceli Ortiz
collection PubMed
description Tumors of the paratesticular region are generally tumors of slow growth, with little symptomatology and, in most cases, benign in nature; in this area, a borderline serous tumor may arise hypothetically from Müllerian metaplasia of the tunica vaginalis, which is histologically identical to its ovarian counterpart. We present a 10-year-old male, with right gynecomastia and ipsilateral hydrocele, showing an enlarged right testicle with a volume of 12 ml and a left testicle with a volume of 10 ml. A right orchiectomy was performed, which presented a poorly defined tan tumor of 1.8 cm that occupied the vaginal and epididymal tunica, and infiltrates the testicular parenchyma. Histological sections revealed a cystic neoplasm, with hierarchical papillary projections, covered by one or several epithelial columnar and hobnail cells with moderate atypia and scant mitosis. Immunohistochemical reactions were performed, resulting positive for PAX-8, epithelial membrane antigen, and CK7, confirming the diagnosis of borderline serous tumor. Since the first reported case in 1986, few have been reported, the majority of these in adults with only three cases in children. In the few cases reported, the prognosis is usually favorable after surgical resection, with disease-free follow-up for up to 18 years.
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spelling pubmed-75919862020-10-30 Paratesticular Serous Borderline Tumor in a Pediatric Patient Meza, Itzel Araceli Ortiz Camacho, Marco Antonio Ponce Márquez, Rodolfo Franco Morquecho, Mauricio Delgado Guajardo, Raquel Garza Quintana, Oralia Barboza Case Rep Pathol Case Report Tumors of the paratesticular region are generally tumors of slow growth, with little symptomatology and, in most cases, benign in nature; in this area, a borderline serous tumor may arise hypothetically from Müllerian metaplasia of the tunica vaginalis, which is histologically identical to its ovarian counterpart. We present a 10-year-old male, with right gynecomastia and ipsilateral hydrocele, showing an enlarged right testicle with a volume of 12 ml and a left testicle with a volume of 10 ml. A right orchiectomy was performed, which presented a poorly defined tan tumor of 1.8 cm that occupied the vaginal and epididymal tunica, and infiltrates the testicular parenchyma. Histological sections revealed a cystic neoplasm, with hierarchical papillary projections, covered by one or several epithelial columnar and hobnail cells with moderate atypia and scant mitosis. Immunohistochemical reactions were performed, resulting positive for PAX-8, epithelial membrane antigen, and CK7, confirming the diagnosis of borderline serous tumor. Since the first reported case in 1986, few have been reported, the majority of these in adults with only three cases in children. In the few cases reported, the prognosis is usually favorable after surgical resection, with disease-free follow-up for up to 18 years. Hindawi 2020-10-19 /pmc/articles/PMC7591986/ /pubmed/33133717 http://dx.doi.org/10.1155/2020/8789143 Text en Copyright © 2020 Itzel Araceli Ortiz Meza et al. https://creativecommons.org/licenses/by/4.0/ 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
Meza, Itzel Araceli Ortiz
Camacho, Marco Antonio Ponce
Márquez, Rodolfo Franco
Morquecho, Mauricio Delgado
Guajardo, Raquel Garza
Quintana, Oralia Barboza
Paratesticular Serous Borderline Tumor in a Pediatric Patient
title Paratesticular Serous Borderline Tumor in a Pediatric Patient
title_full Paratesticular Serous Borderline Tumor in a Pediatric Patient
title_fullStr Paratesticular Serous Borderline Tumor in a Pediatric Patient
title_full_unstemmed Paratesticular Serous Borderline Tumor in a Pediatric Patient
title_short Paratesticular Serous Borderline Tumor in a Pediatric Patient
title_sort paratesticular serous borderline tumor in a pediatric patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591986/
https://www.ncbi.nlm.nih.gov/pubmed/33133717
http://dx.doi.org/10.1155/2020/8789143
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