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Ectopic clival craniopharyngioma.

Golnaz Lotfian1, Akram Al-Warqi2, Santhosh Gaddikeri2

  • 1Department of Diagnostic Radiology and Nuclear Medicine, Rush University Medical Center, Chicago, IL, USA. Lotfian.golnaz@gmail.com.

Neuroradiology
|August 7, 2025
PubMed
Summary

This report details an exceptionally young patient with an ectopic clival craniopharyngioma, a rare tumor. Distinct MRI findings helped differentiate it from chordoma, offering valuable diagnostic insights.

Keywords:
ChordomaCraniopharyngiomaEctopic clival craniopharyngiomaPituitary gland tumor

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Area of Science:

  • Neuro-oncology
  • Pediatric Radiology
  • Pathology

Background:

  • Craniopharyngiomas are rare, benign tumors with bimodal age distribution, often affecting children and older adults.
  • These tumors arise along the craniopharyngeal tract, commonly in intra/suprasellar regions, potentially compressing adjacent structures and causing varied symptoms.
  • Chordomas are distinct rare tumors originating from notochordal remnants, typically in the sacrum or clivus, with characteristic imaging features.

Purpose of the Study:

  • To report a rare case of ectopic clival craniopharyngioma in an 11-year-old, the youngest documented.
  • To highlight unique imaging findings that aid in differentiating this tumor from chordoma.
  • To contribute to the understanding of rare craniopharyngioma presentations.

Main Methods:

  • Case report of an 11-year-old patient with an ectopic clival craniopharyngioma.
  • Diagnostic evaluation utilizing Magnetic Resonance Imaging (MRI).
  • Comparison of imaging characteristics with typical craniopharyngioma and chordoma presentations.

Main Results:

  • The patient presented with an ectopic clival craniopharyngioma extending from the sellar to the clival region.
  • Key imaging findings included T1 hyperintensity and a downward growth pattern along the expected Rathke pouch course.
  • These features were crucial in distinguishing the craniopharyngioma from a chordoma.

Conclusions:

  • Ectopic clival craniopharyngiomas, though rare, can occur in pediatric patients.
  • Specific MRI findings, such as T1 hyperintensity and growth pattern, are vital for accurate diagnosis and differentiation from other skull base tumors like chordoma.
  • This case underscores the importance of detailed imaging analysis in diagnosing rare pediatric neoplasms.