Tumor lysis syndrome in premature infant prompting early resection of a large sacrococcygeal teratoma: a case report

Background Sacrococcygeal teratomas (SCTs) are the most common congenital neoplasm and often require resection soon after birth. There are rare reports of cardiac arrest during surgery due to manipulation of the tumor triggering secondary necrosis and hyperkalemia. Case presentation This case descri...

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Published inBMC pediatrics Vol. 23; no. 1; pp. 1 - 6
Main Authors Dey, Aditi, Wyrebek, Rita, Torres, Loraine, Escoto, Danilo, Shakeel, Fauzia, Mayer, Jennifer
Format Journal Article
LanguageEnglish
Published London BioMed Central Ltd 02.09.2023
BioMed Central
BMC
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Summary:Background Sacrococcygeal teratomas (SCTs) are the most common congenital neoplasm and often require resection soon after birth. There are rare reports of cardiac arrest during surgery due to manipulation of the tumor triggering secondary necrosis and hyperkalemia. Case presentation This case describes a very preterm infant with a SCT who develops spontaneous preoperative tumor lysis syndrome (TLS). The medical team utilized rasburicase and the patient underwent total gross resection at 40 h of life. Conclusions We emphasize the importance of the early recognition and management of tumor lysis syndrome in SCT with rasburicase, aggressive management of hyperkalemia and consideration of early resection of SCTs even in the case of a very premature infant. Keywords: Glucocorticoids, Premature infant, Premature neonates, Rasburicase, Hyperkalemia, Tumor lysis syndrome, Sacrococcygeal teratoma, Neonate
Bibliography:ObjectType-Case Study-2
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ISSN:1471-2431
1471-2431
DOI:10.1186/s12887-023-04193-w