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A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas

OBJECTIVE: The present study aims to discuss the clinical features, treatment, and prognosis of fetal sacrococcygeal teratomas (SCTs) to improve the standard of diagnosis and treatment. METHODS: The clinical data of 15 pregnant females with fetal SCT, admitted to Fujian  Maternity and Child Health H...

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Autores principales: Zheng, Xiu-Qiong, Yan, Jian-Ying, Xu, Rong-Li, Wang, Xue-Chun, Chen, Xian, Huang, Ke-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767721/
https://www.ncbi.nlm.nih.gov/pubmed/33380826
http://dx.doi.org/10.2147/CMAR.S287682
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author Zheng, Xiu-Qiong
Yan, Jian-Ying
Xu, Rong-Li
Wang, Xue-Chun
Chen, Xian
Huang, Ke-Hua
author_facet Zheng, Xiu-Qiong
Yan, Jian-Ying
Xu, Rong-Li
Wang, Xue-Chun
Chen, Xian
Huang, Ke-Hua
author_sort Zheng, Xiu-Qiong
collection PubMed
description OBJECTIVE: The present study aims to discuss the clinical features, treatment, and prognosis of fetal sacrococcygeal teratomas (SCTs) to improve the standard of diagnosis and treatment. METHODS: The clinical data of 15 pregnant females with fetal SCT, admitted to Fujian  Maternity and Child Health Hospital from January 2013 to January 2020, were retrospectively analyzed with respect to clinical characteristics, imaging features, complications, treatment options, and pregnancy outcomes. RESULTS: The 15 cases of fetal SCT were all detected by color ultrasonography. There were two cases of cystic tumors and 13 cases of solid cystic tumors. In terms of tumor blood supply, there was one case without blood flow signal, eight cases with little blood flow signal, and six cases with abundant blood flow. At the time of delivery, there were two cases with a tumor diameter less than 5 cm, five cases with a diameter of 5−10 cm, and eight cases with a diameter of more than 10 cm. In terms of tumor shape and location, there were two cases of type I, ten cases of type II, and three cases of type III. There were six cases with an increased fetal heart to chest ratio, four cases of fetal edema, three cases of placental edema, four cases of excessive amniotic fluid, one case of insufficient amniotic fluid, three cases of fetal distress, one case of stillbirth, two cases of gestational diabetes mellitus, two cases of mirror syndrome, and two cases of postpartum hemorrhage. According to the pathological diagnosis, there were seven cases of mature teratoma, seven cases of immature teratoma, and one case of mixed germ cell tumor. There were six cases of induced delivery, nine cases of cesarean section, one case of premature birth, and two cases of mild neonatal asphyxia. CONCLUSION: Fetal SCT was generally diagnosed by prenatal ultrasonography. The tumor blood supply, growth rate, size, nature of the tumor, clinical type, pathology, and maternal-fetal complications are all closely correlated with the prognosis. The timing and manner of the termination of pregnancy should be determined on the basis of the pregnant female, the fetus, and the tumor.
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spelling pubmed-77677212020-12-29 A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas Zheng, Xiu-Qiong Yan, Jian-Ying Xu, Rong-Li Wang, Xue-Chun Chen, Xian Huang, Ke-Hua Cancer Manag Res Original Research OBJECTIVE: The present study aims to discuss the clinical features, treatment, and prognosis of fetal sacrococcygeal teratomas (SCTs) to improve the standard of diagnosis and treatment. METHODS: The clinical data of 15 pregnant females with fetal SCT, admitted to Fujian  Maternity and Child Health Hospital from January 2013 to January 2020, were retrospectively analyzed with respect to clinical characteristics, imaging features, complications, treatment options, and pregnancy outcomes. RESULTS: The 15 cases of fetal SCT were all detected by color ultrasonography. There were two cases of cystic tumors and 13 cases of solid cystic tumors. In terms of tumor blood supply, there was one case without blood flow signal, eight cases with little blood flow signal, and six cases with abundant blood flow. At the time of delivery, there were two cases with a tumor diameter less than 5 cm, five cases with a diameter of 5−10 cm, and eight cases with a diameter of more than 10 cm. In terms of tumor shape and location, there were two cases of type I, ten cases of type II, and three cases of type III. There were six cases with an increased fetal heart to chest ratio, four cases of fetal edema, three cases of placental edema, four cases of excessive amniotic fluid, one case of insufficient amniotic fluid, three cases of fetal distress, one case of stillbirth, two cases of gestational diabetes mellitus, two cases of mirror syndrome, and two cases of postpartum hemorrhage. According to the pathological diagnosis, there were seven cases of mature teratoma, seven cases of immature teratoma, and one case of mixed germ cell tumor. There were six cases of induced delivery, nine cases of cesarean section, one case of premature birth, and two cases of mild neonatal asphyxia. CONCLUSION: Fetal SCT was generally diagnosed by prenatal ultrasonography. The tumor blood supply, growth rate, size, nature of the tumor, clinical type, pathology, and maternal-fetal complications are all closely correlated with the prognosis. The timing and manner of the termination of pregnancy should be determined on the basis of the pregnant female, the fetus, and the tumor. Dove 2020-12-23 /pmc/articles/PMC7767721/ /pubmed/33380826 http://dx.doi.org/10.2147/CMAR.S287682 Text en © 2020 Zheng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zheng, Xiu-Qiong
Yan, Jian-Ying
Xu, Rong-Li
Wang, Xue-Chun
Chen, Xian
Huang, Ke-Hua
A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title_full A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title_fullStr A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title_full_unstemmed A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title_short A Clinical Analysis of the Diagnosis and Treatment of Fetal Sacrococcygeal Teratomas
title_sort clinical analysis of the diagnosis and treatment of fetal sacrococcygeal teratomas
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767721/
https://www.ncbi.nlm.nih.gov/pubmed/33380826
http://dx.doi.org/10.2147/CMAR.S287682
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