Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mindaye, Esubalew T., Kassahun, Mulugeta, Prager, Sarah, Tufa, Tesfaye H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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
_version_ 1783613583692660736
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
work_keys_str_mv AT mindayeesubalewt adultcaseofgiantsacrococcygealteratomacasereport
AT kassahunmulugeta adultcaseofgiantsacrococcygealteratomacasereport
AT pragersarah adultcaseofgiantsacrococcygealteratomacasereport
AT tufatesfayeh adultcaseofgiantsacrococcygealteratomacasereport