Publication:
Sacrococcygeal Teratoma in a Child: A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorRoka, Yam B
dc.contributor.authorShrestha, Manzil
dc.contributor.authorPandey, Sagar R
dc.date.accessioned2026-06-09T10:12:15Z
dc.date.available2026-06-09T10:12:15Z
dc.date.issued2010
dc.descriptionYam B Roka Chief of Neurosurgery, Neuro Hospital, Jahada Road, Biratnagar-13 Manzil Shrestha Division of Anaesthesiology, Neuro Hospital, Jahada Road, Biratnagar-13 Sagar R Pandey Division of Pathology, Neuro Hospital, Jahada Road, Biratnagar-13
dc.description.abstractAbstract: Sacrococcygeal teratomas (SCT) are tumors that arise in the sacrococcygeal area containing tissue from all three germ layers. SCT has an incidence of approximately one in 35,000 – 40,000 live births with malignant transformation with increasing age. We report a case in a four year old which was excised completely via the postanal route with no operative or postoperative morbidity. The histopathology was that of yolk sac variant and she is planned for chemoradiotherapy.
dc.identifierhttps://doi.org/10.3126/jnps.v30i2.3450
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6389
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectChildhood tumors
dc.subjectSacrum
dc.subjectSacrococcygeal teratoma
dc.titleSacrococcygeal Teratoma in a Child: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage115
oaire.citation.startPage113
relation.isJournalIssueOfPublication41c25f76-4829-4dfd-bfd4-e961ed857798
relation.isJournalIssueOfPublication.latestForDiscovery41c25f76-4829-4dfd-bfd4-e961ed857798
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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