persistierender Canalis craniopharyngealis

Persistent hypophyseal canal, also known as the craniopharyngeal canal when larger than 1.5 mm in diameter, is a rare congenital defect characterized by a communication through the central skull base between the nasopharynx and the pituitary fossa.


There are a number of terms which refer to this abnormality and some authors distinguish between canals based on whether they are larger or smaller than 1.5 mm in diameter. To avoid confusion:

  • a canal less than 1.5 mm in diameter
    • persistent hypophyseal canal
  • a canal greater than 1.5 mm in diameter
    • craniopharyngeal canal
    • large craniopharyngeal canal
    • transphenoidal canal

The remainder of this article will refer to the defect as a persistent hypophyseal canal, keeping in mind that when large, alternative terms are preferable.

Additionally, the larger defects are possibly more closely related to transsphenoidal meningoencephaloceles than to persistent hypophyseal canals .


The prevalence of persistent hypophyseal canals has been reported to be as high as 0.42% .

Clinical presentation

In most cases, individuals with a persistent canal are asymptomatic. Possible presentations include :

In addition, many craniofacial anomalies have been reported, especially with the larger defects, including :


The exact cause of these defects is uncertain, as is whether or not they all share the same underlying etiology. Two theories have been proposed:

  • persistence of Rathke's pouch
  • persistence of a vascular channel
  • Radiographic features

    Persistent hypophyseal canals, as well as the larger craniopharyngeal canals, are found in the midline, oriented vertically and extending form the floor of the pituitary fossa to the posterior wall of the nasopharynx, passing behind the sphenoid sinus.


    They are best appreciated on thin slice bone filter CT, and appear as a sharply circumscribed corticated canal.

    Differential diagnosis

    Siehe auch: