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DOI: 10.1590/0004-282X20180120
Persistent craniopharyngeal canal
Canal craniofaríngeo persistenteA two-year-old male, with delayed neuropsychomotor development underwent computed tomography and magnetic resonance imaging ([Figure]). The diagnosis was persistent craniopharyngeal canal.


Persistent craniopharyngeal canal is a rare congenital anomaly of the skull base and is defined as a well-corticated osseous canal, extending from the roof of the nasopharynx to the base of the sella, over the sphenoid corpus, allowing the pituitary gland to present as a nasopharyngeal mass. Its origin may represent the remnant of the route of Rathke's pouch[1]. Computed tomography and magnetic resonance imaging evaluate the content and limits of the canal well, preventing surgical iatrogenesis, such as hypopituitarism and cerebrospinal fluid leakage[2].
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Conflict of interest:
There is no conflict of interest to declare.
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References
- 1 Akyel NG, Alimli AG, Demirkan TH, Sivri M. Persistent craniopharyngeal canal, bilateral microphthalmia with colobomatous cysts, ectopic adenohypophysis with Rathke cleft cyst, and ectopic neurohypophysis: case report and review of the literature. Childs Nerv Syst. 2018 Jul;34(7):1407-10. https://doi.org/10.1007/s00381-018-3747-4
- 2 Mohindra S, Gupta K, Mohindra S. A novel minimally invasive endoscopic repair in a case of spontaneous CSF rhinorrhea with persistent craniopharyngeal canal. NeurolIndia. 2015;63(3):434-6. https://doi.org/10.4103/0028-3886.158243
Address for correspondence
Publikationsverlauf
Eingereicht: 16. April 2018
Angenommen: 08. August 2018
Artikel online veröffentlicht:
22. August 2023
© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Akyel NG, Alimli AG, Demirkan TH, Sivri M. Persistent craniopharyngeal canal, bilateral microphthalmia with colobomatous cysts, ectopic adenohypophysis with Rathke cleft cyst, and ectopic neurohypophysis: case report and review of the literature. Childs Nerv Syst. 2018 Jul;34(7):1407-10. https://doi.org/10.1007/s00381-018-3747-4
- 2 Mohindra S, Gupta K, Mohindra S. A novel minimally invasive endoscopic repair in a case of spontaneous CSF rhinorrhea with persistent craniopharyngeal canal. NeurolIndia. 2015;63(3):434-6. https://doi.org/10.4103/0028-3886.158243

