Atypical presacral masses in Currarino syndrome: a case series.

Childs Nerv SystOct 13, 2026 (epub)

Ravi Ameet Patel, Rebecca Du, Erin Rowell et al.

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Case in brief

The report describes three patients with Currarino syndrome, a congenital condition involving a sacral anomaly, anorectal malformation, and presacral mass. Pathologic examination identified a myxopapillary ependymoma associated with a retrorectal teratoma, a mature cystic teratoma, and a neuroendocrine tumor arising within a teratoma. The cases demonstrate that presacral lesions in this syndrome can include tumors beyond the commonly reported anterior meningoceles and teratomas. The authors emphasize that surgical management should be individualized and may require a multidisciplinary approach.

What made this case unusual

The cases included a myxopapillary ependymoma associated with a retrorectal teratoma and a neuroendocrine tumor arising within a teratoma—tumor types the authors identify as underrecognized or previously unreported in Currarino syndrome.

Diagnostic / clinical pearl

Do not assume a presacral mass in Currarino syndrome is an anterior meningocele or a conventional teratoma; pathologic assessment may reveal a broader range of lesions.

Why it matters

Recognizing this lesion heterogeneity supports thorough evaluation and individualized, often multidisciplinary, surgical planning.

Source

Published in Childs Nerv Syst. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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