Prenatal Sacrococcygeal Teratoma Diagnosed in a Fetus with Partial Trisomy 13q22

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Sacrococcygeal Teratoma associated with Trisomy 13

Sacrococcygeal teratoma (SCT) is rarely associated with syndromes. We report a female newborn with a prenatal diagnosis of small sacrococcygeal teratoma and postnatally diagnosed as having trisomy 13. The sacrococcygeal teratoma was excised. It was reported as mature teratoma. The child succumbed to sepsis postoperatively.

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We report a case in which a sacrococcygeal teratoma was identified and characterized on prenatal and postnatal MRI, and correlated with subsequent surgical resection.

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Sacrococcygeal Teratoma: A Case Report

Background: Neonatal tumors are usually prenatally diagnosed or within the irst 30 days of life. The true incidence ofneonatal tumors is unknown as a great number of pregnancies with a prenatally diagnosed mass result in stillbirth ormiscarriage. Most solid neonatal tumors are benign whereas less than 50% of neonatal neoplasms are malignant;however, some tumors with malignant ...

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SACROCOCCYGEAL TERATOMA

31 cases of sacrococcygeal teratoma from the Children's Hospital of Ziirich and 25 cases from the Children's Hospital of Tehran are evaluated and compared. In seven cases the tumors were organized. They contained parts of organs or rudimentary extremities. According to general experience the malignancy of tumors is higher in children who are operated on after their second to fourth month o...

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Prenatal sonographic diagnosis of congenital sacrococcygeal teratoma and management.

Teratomas are tumors containing tissues derived from all three germinal cell layers. Most teratomas arise in the sacrococcygeal region, with a reported incidence of 1/40,000 births. During labor, severe dystocia may occur in infants with large tumors if delivered vaginally, with an extremely high fetal morbidity and mortality rate. Reported is a case of a large congenital sacrococcygeal teratom...

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ژورنال

عنوان ژورنال: Case Reports in Obstetrics and Gynecology

سال: 2019

ISSN: 2090-6684,2090-6692

DOI: 10.1155/2019/2892869