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A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos
BACKGROUND: Sacrococcygeal teratomas (SCTs) are known to cause urological complications, but urethrovaginal (UV) fistula as a complication of SCT is rare. We herein report a case of SCT with UV fistula and hydrocolpos. CASE PRESENTATION: A 1-day-old female neonate presented to our department with pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616020/ https://www.ncbi.nlm.nih.gov/pubmed/37903968 http://dx.doi.org/10.1186/s40792-023-01772-y |
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author | Shibui, Yuichi Obata, Satoshi Hirose, Ryuichiro Nakano, Ryo Setoue, Takashi Miyazaki, Takeshi Matsuoka, Hirofumi Sato, Toshihiko |
author_facet | Shibui, Yuichi Obata, Satoshi Hirose, Ryuichiro Nakano, Ryo Setoue, Takashi Miyazaki, Takeshi Matsuoka, Hirofumi Sato, Toshihiko |
author_sort | Shibui, Yuichi |
collection | PubMed |
description | BACKGROUND: Sacrococcygeal teratomas (SCTs) are known to cause urological complications, but urethrovaginal (UV) fistula as a complication of SCT is rare. We herein report a case of SCT with UV fistula and hydrocolpos. CASE PRESENTATION: A 1-day-old female neonate presented to our department with prominent swelling in the sacrococcygeal region. She was born at 37 gestational weeks via spontaneous vaginal delivery from a 39-year-old woman. The weight of the baby was 2965 g, and her Apgar scores were 4/10 (at 1 and 5 min). An MRI examination confirmed an 11 × 11 cm Altman classification typeII SCT associated with hydrocolpos, a dilated urinary bladder, and bilateral hydronephrosis. When she was 5 days, the SCT was excised totally and a coccygectomy was performed. After the operation, as her urinary output appeared unstable, a cystoscopic examination was performed on the third postoperative day. This revealed that the UV fistula was located approximately 1 cm from the urethral opening. In addition, the proximal urethra was unobstructed and connected to the bladder. The cystoscope allowed for the passage of a urinary catheter through the urethra. After 1 month of catheter placement, she was discharged from the hospital at 57 days of age. Follow-up was uneventful, with neither urinary infection nor retention. CONCLUSIONS: SCTs are associated with not only trouble with rectal function and lower extremity movement but also urinary complications. The pathogenesis of this UV fistula is thought to be the rapid growth of the SCT that developed in the fetal period, resulting in obstruction of the urethra by the tumor and the pubic bone, which in turn caused urinary retention and the formation of a fistula as an escape route for the pressure. Because SCTs can cause a variety of complications depending on the course of the disease, careful examination and follow-up are necessary. |
format | Online Article Text |
id | pubmed-10616020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106160202023-11-01 A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos Shibui, Yuichi Obata, Satoshi Hirose, Ryuichiro Nakano, Ryo Setoue, Takashi Miyazaki, Takeshi Matsuoka, Hirofumi Sato, Toshihiko Surg Case Rep Case Report BACKGROUND: Sacrococcygeal teratomas (SCTs) are known to cause urological complications, but urethrovaginal (UV) fistula as a complication of SCT is rare. We herein report a case of SCT with UV fistula and hydrocolpos. CASE PRESENTATION: A 1-day-old female neonate presented to our department with prominent swelling in the sacrococcygeal region. She was born at 37 gestational weeks via spontaneous vaginal delivery from a 39-year-old woman. The weight of the baby was 2965 g, and her Apgar scores were 4/10 (at 1 and 5 min). An MRI examination confirmed an 11 × 11 cm Altman classification typeII SCT associated with hydrocolpos, a dilated urinary bladder, and bilateral hydronephrosis. When she was 5 days, the SCT was excised totally and a coccygectomy was performed. After the operation, as her urinary output appeared unstable, a cystoscopic examination was performed on the third postoperative day. This revealed that the UV fistula was located approximately 1 cm from the urethral opening. In addition, the proximal urethra was unobstructed and connected to the bladder. The cystoscope allowed for the passage of a urinary catheter through the urethra. After 1 month of catheter placement, she was discharged from the hospital at 57 days of age. Follow-up was uneventful, with neither urinary infection nor retention. CONCLUSIONS: SCTs are associated with not only trouble with rectal function and lower extremity movement but also urinary complications. The pathogenesis of this UV fistula is thought to be the rapid growth of the SCT that developed in the fetal period, resulting in obstruction of the urethra by the tumor and the pubic bone, which in turn caused urinary retention and the formation of a fistula as an escape route for the pressure. Because SCTs can cause a variety of complications depending on the course of the disease, careful examination and follow-up are necessary. Springer Berlin Heidelberg 2023-10-31 /pmc/articles/PMC10616020/ /pubmed/37903968 http://dx.doi.org/10.1186/s40792-023-01772-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Shibui, Yuichi Obata, Satoshi Hirose, Ryuichiro Nakano, Ryo Setoue, Takashi Miyazaki, Takeshi Matsuoka, Hirofumi Sato, Toshihiko A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title | A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title_full | A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title_fullStr | A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title_full_unstemmed | A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title_short | A case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
title_sort | case of sacrococcygeal teratoma associated with antenatally acquired urethrovaginal fistula and hydrocolpos |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616020/ https://www.ncbi.nlm.nih.gov/pubmed/37903968 http://dx.doi.org/10.1186/s40792-023-01772-y |
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