Abstract
We describe the case of a 4-year-old female who was born with persistent cloaca and was subsequently diagnosed with posterior mediastinal neuroblastoma. To our knowledge, this is the first case report of neuroblastoma associated with a cloacal malformation. Neither neuroblastoma nor persistent cloaca has a high incidence among the general population. Therefore, we share this case as a rare association of conditions, as well as a potential area for further investigation.
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