Published online Feb 29, 2016.
https://doi.org/10.3348/jksr.2016.74.3.210
Persistent Craniopharyngeal Canal with Posterior Pituitary Ectopia: A Case Report
Abstract
Persistent craniopharyngeal canal is a congenital defect between sella turcica and nasopharynx. It is considered to develope from incomplete closure of Rathke's pouch, the precursor of adenohypophysis. Persistent craniopharyngeal canal can be associated pituitary anomalies and other central nervous system anomalies. We presented a case of persistent craniopharyngeal canal with posterior pituitary ectopia.
Fig. 1
B. Gadolinium enhanced T1-weighted sagittal MR image reveals prominent enhancement of soft tissue lesion at the inferior aspect of sella turcica (*), presumably the meninges with possible aplasia or hypoplasia of anterior pituitary lobe.
A 16-month-old boy with posterior pituitary ectopia.
A. T1-weighted MR sagittal image shows that normally T1-hyperintense posterior pituitary lobe is absent within sella turcica, and small bright high signal intensity lesion is located at the median eminence, anterior to the mammillary body (arrow), suggesting ectopic posterior pituitary lobe. Ill-defined isointense soft tissue lesion is seen at the inferior aspect of sella turcica (*), but normal anterior pituitary lobe is absent. A cortical defect is suspected at the anteroinferior wall of sella turcica (arrowhead).
Fig. 2
Persistent craniopharyngeal canal.
Axial (A), sagittal (B), and coronal (C) CT images of bone window setting show a cortical defect of the sella floor with a corticated canal between sella turcica and nasopharynx (arrow). It reveals a persistent craniopharyngeal canal. Incidental ethmoid sinusitis is also noted.
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