Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome

Sacrococcygeal teratoma (SCT) occurs in approximately 1 per 20,000–40,000 births and is the most frequently encountered fetal teratoma, with 75% of cases observed in female fetuses. SCT can be detected on ultrasound as early as the first trimester, presenting as a large mass originating from the sa...

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Main Authors: Anna Kornete, Diana Bokucava, Natalija Vedmedovska
Format: Article
Language:English
Published: Vilnius University Press 2023-11-01
Series:Acta Medica Lituanica
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Online Access:https://www.zurnalai.vu.lt/AML/article/view/32645
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author Anna Kornete
Diana Bokucava
Natalija Vedmedovska
author_facet Anna Kornete
Diana Bokucava
Natalija Vedmedovska
author_sort Anna Kornete
collection DOAJ
description Sacrococcygeal teratoma (SCT) occurs in approximately 1 per 20,000–40,000 births and is the most frequently encountered fetal teratoma, with 75% of cases observed in female fetuses. SCT can be detected on ultrasound as early as the first trimester, presenting as a large mass originating from the sacrococcygeal area, with or without an intrapelvic component. The prenatal course for most fetuses with SCT is generally uneventful, with only a few cases experiencing obstetric and fetal complications. We present the case of a 19-year-old woman who was in good health and had no relevant family or medical history. She was gravida 2 and para 1. During the first trimester scan, an examination revealed a heterogeneous mass in the presacral area with a predominantly multicystic appearance, measuring 12 mm in diameter. At 21+6 weeks of gestation, the Type 2 fetal SCT showed an increase in volume with the size of 49×37×36 mm and contiune to increase in size. The male fetus was delivered by elective Cesarean section at 38 weeks of gestation. The resection of the tumor and coccyx was performed when the newborn was 7 days old. The tumor measured 190×160×100 mm and weighed 1100 g. Pathological examination confirmed the diagnosis of a mature teratoma (Grade 0), and the resection margins were negative. Our case report highlights a fetus with a large and rapidly growing SCT, yet the outcome was excellent.
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spelling doaj-art-03eea578da9247e8a970be10d882b1ce2025-02-11T18:08:40ZengVilnius University PressActa Medica Lituanica1392-01382029-41742023-11-0130210.15388/Amed.2023.30.2.13Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent OutcomeAnna Kornete0Diana Bokucava1Natalija Vedmedovska2Riga Stradiņš University, LatviaDepartment of Obstetrics and Gynaecology, Riga Stradiņš University, LatviaDepartment of Obstetrics and Gynaecology, Riga Stradiņš University, Latvia Sacrococcygeal teratoma (SCT) occurs in approximately 1 per 20,000–40,000 births and is the most frequently encountered fetal teratoma, with 75% of cases observed in female fetuses. SCT can be detected on ultrasound as early as the first trimester, presenting as a large mass originating from the sacrococcygeal area, with or without an intrapelvic component. The prenatal course for most fetuses with SCT is generally uneventful, with only a few cases experiencing obstetric and fetal complications. We present the case of a 19-year-old woman who was in good health and had no relevant family or medical history. She was gravida 2 and para 1. During the first trimester scan, an examination revealed a heterogeneous mass in the presacral area with a predominantly multicystic appearance, measuring 12 mm in diameter. At 21+6 weeks of gestation, the Type 2 fetal SCT showed an increase in volume with the size of 49×37×36 mm and contiune to increase in size. The male fetus was delivered by elective Cesarean section at 38 weeks of gestation. The resection of the tumor and coccyx was performed when the newborn was 7 days old. The tumor measured 190×160×100 mm and weighed 1100 g. Pathological examination confirmed the diagnosis of a mature teratoma (Grade 0), and the resection margins were negative. Our case report highlights a fetus with a large and rapidly growing SCT, yet the outcome was excellent. https://www.zurnalai.vu.lt/AML/article/view/32645sacrococcygeal teratomasprenatal diagnosticvascular indexalpha-fetoprotein
spellingShingle Anna Kornete
Diana Bokucava
Natalija Vedmedovska
Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
Acta Medica Lituanica
sacrococcygeal teratomas
prenatal diagnostic
vascular index
alpha-fetoprotein
title Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
title_full Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
title_fullStr Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
title_full_unstemmed Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
title_short Fetal Sacrococcygeal Teratoma: A Case Report of a Giant Tumor with an Excellent Outcome
title_sort fetal sacrococcygeal teratoma a case report of a giant tumor with an excellent outcome
topic sacrococcygeal teratomas
prenatal diagnostic
vascular index
alpha-fetoprotein
url https://www.zurnalai.vu.lt/AML/article/view/32645
work_keys_str_mv AT annakornete fetalsacrococcygealteratomaacasereportofagianttumorwithanexcellentoutcome
AT dianabokucava fetalsacrococcygealteratomaacasereportofagianttumorwithanexcellentoutcome
AT natalijavedmedovska fetalsacrococcygealteratomaacasereportofagianttumorwithanexcellentoutcome