Craniopharyngioma in the Prepontine Cistern

Letters to the Editor Letters to the Editor

Published ahead of print on January 13, 2011
doi: 10.3174/ajnr.A2467

American Journal of Neuroradiology 32:E57, March 2011
© 2011 American Society of Neuroradiology

I.H. Leea, C.J. Songa and J.S. Yeona
aDepartment of Radiology

S.-H. Kimb
bDepartment of Neurosurgery

K.-S. Songc and M.-K. Yeoc
cDepartment of Pathology
Chungnam National University Hospital
Chungnam National University School of Medicine
Daejeon
South Korea

We report a pathologically proved craniopharyngioma in the prepontine cistern. A 50-year-old woman presented with swallowing difficulty for 1 month. She underwent brain MR and CT imaging.

T1-weighted, T2-weighted, and contrast-enhanced T1-weighted images showed a large peripheral enhancing cystic mass in the prepontine cistern. Inside the lesion, high signal intensity (SI) on T1 and low SI on T2-weighted imaging were noted (Fig 1). The CT scan showed features similar to those on the MR images, except for the addition of a peripheral small calcification in the cystic lesion. We could not find any connection between the mass in the prepontine cistern and the sellar or parasellar area. The mass was partially surgically removed, and histopathologic examination revealed craniopharyngioma in the prepontine cistern.

  • Figure 1
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  • Fig 1. A 50-year-old woman with a craniopharyngioma in the prepontine cistern. A, Sagittal T1-weighted image shows a cystic mass in the prepontine cistern. B, Contrast-enhanced T1-weighted sagittal image shows a peripheral enhancing cystic mass in the prepontine cistern.

Craniopharyngiomas can arise anywhere along the craniopharyngeal canal. However, there are several reports of craniopharyngiomas with unusual locations—that is, in the posterior cranial fossa, without a connection to the sellar or parasellar area. The locations were the temporal lobe, pons and fourth ventricle, and cerebellopontine angle and fourth ventricle.1–3

In our case, the location was the prepontine cistern, which was not previously described, to our knowledge. Considering the location of the craniopharyngioma in our patient in contrast to the usual location, the hypothesis that most craniopharyngiomas occur along the craniopharyngeal canal could not be applied. Instead, the suggestion of Solarski et al,4—that is, ectopic craniopharyngiomas might originate from totipotential or multipotential cells—might be applied to our case.

In conclusion, although the location in our patient was very unusual, craniopharyngiomas can occur anywhere.

References

  1. Sohn CH, Baik SK, Kim SP, et al. Craniopharyngioma in the temporal lobe: a case report. Korean J Radiol2004;5:72–74[Medline]
  2. Shah GB, Bhaduri AS, Misra BK. Ectopic craniopharyngioma of the fourth ventricle: case report. Surg Neurol2007;68:96–98[CrossRef][Medline]
  3. Bashir EM, Lewis PD, Edwards MR. Posterior fast craniopharyngioma. Br J Neurosurg 1996;10:613–15[CrossRef][Medline]
  4. Solarski A, Panke ES, Panke TW. Craniopharyngioma in the pineal gland. Arch Pathol Lab Med 1978;102:490–91[Medline]

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