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Update in the prenatal management of sacrococcygeal teratomas and the outcome of the newborn – case report
Author(s) -
Bianca Margareta Mihai,
Roxana Elena Bohîlţea,
Vlad Dima,
Alina Veduță,
Teodor Salmen,
Tiberiu Augustin Georgescu,
Maria Irina Vlădăreanu,
Valentin-Nicolae Varlas
Publication year - 2021
Publication title -
romanian journal of pediatrics
Language(s) - English
Resource type - Journals
eISSN - 2069-6175
pISSN - 1454-0398
DOI - 10.37897/rjp.2021.3.5
Subject(s) - sacrococcygeal teratoma , medicine , fetus , teratoma , cardiac decompensation , pregnancy , in utero , etiology , decompensation , obstetrics , prenatal diagnosis , heart failure , pediatrics , surgery , pathology , cardiology , genetics , biology
Sacrococcygeal teratomas complicate approximatively 1 in 27,000 pregnancies, being the most common congenital germ cell tumors in infants. The diagnosis is suspected using ultrasonographic examination and confirmed after a pathology report is performed. The main issue complicating fetuses with sacrococcygeal teratomas is represented by the rapid growth and the great need of blood supply captured by the tumor that interferes with the fetal growth and fetal wellbeing, generating heart failure and, unfortunately, increasing neonatal mortality. Thus, ultrasonographic monitoring is fundamental, to diagnose, closely monitor the growth and vascularization of the tumor and to ameliorate the neonatal prognosis by establishing the proper time of birth. There are specialized healthcare centers that could perform in utero surgery with the aim to aid the normal growth and development of the fetus until term, when a curative surgery is performed to the newborn. In cases complicated with heart failure leading to fetal hydrops, pregnancy termination could be a valuable option for the mothers, as soon as the etiology and the stage of heart decompensation are known. We present a case of a fetal sacrococcygeal teratoma in a 36-year-old pregnant woman, an uninvestigated pregnancy that had a dreadful outcome with neonatal death.

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