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 in | BMC pediatrics Vol. 23; no. 1; pp. 1 - 6 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central Ltd
02.09.2023
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
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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 |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 1471-2431 1471-2431 |
DOI: | 10.1186/s12887-023-04193-w |