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Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features
Accessory scrotum (AS) is rarely diagnosed antenatally, and its prenatal features remain unknown. Here, we report a case of a prenatally diagnosed accessory scrotum with perineal lipoma. A 33-year-old woman was referred to our hospital at 35 weeks of gestation to evaluate a mass in the fetal perinea...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760351/ https://www.ncbi.nlm.nih.gov/pubmed/35059092 http://dx.doi.org/10.1016/j.radcr.2021.12.033 |
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author | Deguchi, Koichi Tazuke, Yuko Watanabe, Miho Toyama, Chiyoshi Nomura, Motonari Saka, Ryuta Harada, Hiromi Nagamine, Yukie Endo, Masayuki Puh, Ritsuko Okuyama, Hiroomi |
author_facet | Deguchi, Koichi Tazuke, Yuko Watanabe, Miho Toyama, Chiyoshi Nomura, Motonari Saka, Ryuta Harada, Hiromi Nagamine, Yukie Endo, Masayuki Puh, Ritsuko Okuyama, Hiroomi |
author_sort | Deguchi, Koichi |
collection | PubMed |
description | Accessory scrotum (AS) is rarely diagnosed antenatally, and its prenatal features remain unknown. Here, we report a case of a prenatally diagnosed accessory scrotum with perineal lipoma. A 33-year-old woman was referred to our hospital at 35 weeks of gestation to evaluate a mass in the fetal perineal region. Prenatal ultrasonography showed a 2.0 × 2.0 cm sized, echogenic, and circular mass located posterior to the left scrotum in a male fetus. Magnetic resonance imaging (MRI) showed a mass containing adipose tissue. A 6.5 cm elastic mass (AS and protruding lipoma) was observed in the perineal region, and surgical excision was performed at 8 months of age. Histological examination confirmed the diagnosis of AS with perineal lipoma, and there was no recurrence at follow-up. The typical prenatal presentation of AS was a circular perineal mass located posterior to the normal scrotum and was associated with perineal lipoma. The prenatal detection of AS was feasible with careful observation via ultrasonography, and prenatal MRI was useful in characterizing perineal tumors and evaluating associated anomalies. |
format | Online Article Text |
id | pubmed-8760351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87603512022-01-19 Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features Deguchi, Koichi Tazuke, Yuko Watanabe, Miho Toyama, Chiyoshi Nomura, Motonari Saka, Ryuta Harada, Hiromi Nagamine, Yukie Endo, Masayuki Puh, Ritsuko Okuyama, Hiroomi Radiol Case Rep Case Report Accessory scrotum (AS) is rarely diagnosed antenatally, and its prenatal features remain unknown. Here, we report a case of a prenatally diagnosed accessory scrotum with perineal lipoma. A 33-year-old woman was referred to our hospital at 35 weeks of gestation to evaluate a mass in the fetal perineal region. Prenatal ultrasonography showed a 2.0 × 2.0 cm sized, echogenic, and circular mass located posterior to the left scrotum in a male fetus. Magnetic resonance imaging (MRI) showed a mass containing adipose tissue. A 6.5 cm elastic mass (AS and protruding lipoma) was observed in the perineal region, and surgical excision was performed at 8 months of age. Histological examination confirmed the diagnosis of AS with perineal lipoma, and there was no recurrence at follow-up. The typical prenatal presentation of AS was a circular perineal mass located posterior to the normal scrotum and was associated with perineal lipoma. The prenatal detection of AS was feasible with careful observation via ultrasonography, and prenatal MRI was useful in characterizing perineal tumors and evaluating associated anomalies. Elsevier 2022-01-12 /pmc/articles/PMC8760351/ /pubmed/35059092 http://dx.doi.org/10.1016/j.radcr.2021.12.033 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Deguchi, Koichi Tazuke, Yuko Watanabe, Miho Toyama, Chiyoshi Nomura, Motonari Saka, Ryuta Harada, Hiromi Nagamine, Yukie Endo, Masayuki Puh, Ritsuko Okuyama, Hiroomi Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title | Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title_full | Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title_fullStr | Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title_full_unstemmed | Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title_short | Prenatally diagnosed accessory scrotum: A case report and review of the literature on prenatal features |
title_sort | prenatally diagnosed accessory scrotum: a case report and review of the literature on prenatal features |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760351/ https://www.ncbi.nlm.nih.gov/pubmed/35059092 http://dx.doi.org/10.1016/j.radcr.2021.12.033 |
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