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Adult case of giant sacrococcygeal teratoma: case report
BACKGROUND: Sacrococcygeal teratomas are tumors originating from pluripotent embryonic germ cell layers located in the fetal coccyx. These tumors are highly vascular if they undergo malignant transformation. Typically, they are found in infants and children and occasionally can be diagnosed prenatal...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687728/ https://www.ncbi.nlm.nih.gov/pubmed/33234106 http://dx.doi.org/10.1186/s12893-020-00962-x |
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author | Mindaye, Esubalew T. Kassahun, Mulugeta Prager, Sarah Tufa, Tesfaye H. |
author_facet | Mindaye, Esubalew T. Kassahun, Mulugeta Prager, Sarah Tufa, Tesfaye H. |
author_sort | Mindaye, Esubalew T. |
collection | PubMed |
description | BACKGROUND: Sacrococcygeal teratomas are tumors originating from pluripotent embryonic germ cell layers located in the fetal coccyx. These tumors are highly vascular if they undergo malignant transformation. Typically, they are found in infants and children and occasionally can be diagnosed prenatally. Adult cases are very rare, and represent tumors present since birth with delayed detection. CASE PRESENTATION: We describe a case of a giant sacrococcygeal teratoma in a 25 years old female college student presenting with right gluteal swelling of 4 months’ duration. In addition to the huge disfiguring mass on the perineal area, she also had lower abdominal pain, urinary complaints, and difficulty with ambulation. DISCUSSION: Pre-operative impression was of a sacrococcygeal mass and histopathology following complete surgical excision revealed a sacrococcygeal teratoma. She recovered well after surgery with no radiologic evidence of recurrence at six months. CONCLUSION: Although rare, sacrococcygeal teratoma should be considered as a differential diagnosis for female adults presenting with perineal and/or pelvic masses. Complete surgical excision remains the mainstay of treatment. |
format | Online Article Text |
id | pubmed-7687728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76877282020-11-30 Adult case of giant sacrococcygeal teratoma: case report Mindaye, Esubalew T. Kassahun, Mulugeta Prager, Sarah Tufa, Tesfaye H. BMC Surg Case Report BACKGROUND: Sacrococcygeal teratomas are tumors originating from pluripotent embryonic germ cell layers located in the fetal coccyx. These tumors are highly vascular if they undergo malignant transformation. Typically, they are found in infants and children and occasionally can be diagnosed prenatally. Adult cases are very rare, and represent tumors present since birth with delayed detection. CASE PRESENTATION: We describe a case of a giant sacrococcygeal teratoma in a 25 years old female college student presenting with right gluteal swelling of 4 months’ duration. In addition to the huge disfiguring mass on the perineal area, she also had lower abdominal pain, urinary complaints, and difficulty with ambulation. DISCUSSION: Pre-operative impression was of a sacrococcygeal mass and histopathology following complete surgical excision revealed a sacrococcygeal teratoma. She recovered well after surgery with no radiologic evidence of recurrence at six months. CONCLUSION: Although rare, sacrococcygeal teratoma should be considered as a differential diagnosis for female adults presenting with perineal and/or pelvic masses. Complete surgical excision remains the mainstay of treatment. BioMed Central 2020-11-24 /pmc/articles/PMC7687728/ /pubmed/33234106 http://dx.doi.org/10.1186/s12893-020-00962-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Mindaye, Esubalew T. Kassahun, Mulugeta Prager, Sarah Tufa, Tesfaye H. Adult case of giant sacrococcygeal teratoma: case report |
title | Adult case of giant sacrococcygeal teratoma: case report |
title_full | Adult case of giant sacrococcygeal teratoma: case report |
title_fullStr | Adult case of giant sacrococcygeal teratoma: case report |
title_full_unstemmed | Adult case of giant sacrococcygeal teratoma: case report |
title_short | Adult case of giant sacrococcygeal teratoma: case report |
title_sort | adult case of giant sacrococcygeal teratoma: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687728/ https://www.ncbi.nlm.nih.gov/pubmed/33234106 http://dx.doi.org/10.1186/s12893-020-00962-x |
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