AJDRAJNR - American Journal of Neuroradiology

This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marsot-Dupuch, K.
Right arrow Articles by Grauer, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marsot-Dupuch, K.
Right arrow Articles by Grauer, W.

Case Report
BRAIN

A Rare Expression of Neural Crest Disorders: An Intrasphenoidal Development of the Anterior Pituitary Gland

Kathlyn Marsot-Dupucha, Wendy R. K. Smokerb and Walter Grauerc

a Department of NeuroRadiology, Faculty Paris Sud, le Kremlin-Bicêtre, France
b Department of Radiology, University of Iowa Hospitals and Clinics, Iowa City, IA
c Department of Department of Radiology, Bethanien Spital, Zurich, Switzerland

Address reprint requests and correspondence to Dr. Kathlyn Marsot-Dupuch Bicêtre Hospital-Neuroradiology, 78 rue du Général Leclerc. Kremlin-Bicêtre, France 94 275

Summary: Congenital abnormalities of the pituitary gland are rare and may be associated with midline cranial, orbital, and facial anomalies and with hormonal insufficiency. Here we report a case of asymptomatic, abnormal migration of the adenohypophysis. The normally developed adenohypophysis was located in the sphenoid bone and developed on the intersphenoidal septum, extending from the superior pharyngeal wall to the floor of the sella turcica (craniopharyngeal canal). The abnormal migration of the pituitary gland was isolated without hormonal deficit, brain, or facial developmental anomalies.