Absent sella turcica: a case report and a review of the literature

Fetal Pediatr Pathol. 2013 Oct;32(5):375-83. doi: 10.3109/15513815.2013.799249. Epub 2013 May 20.

Abstract

Absent sella turcica is an extremely rare and dramatic radiographic finding. It may be isolated or occur in the presence of other anomalies, often involving the adenohypophysis. Our evaluation of a female infant with multiple anomalies including absence of the sella turcica, a normal pituitary in the craniopharyngeal canal, normal pituitary function, choanal atresia and anomalies of the appendiceal skeleton prompted a review of the occurrence and biology of an absent sella turcica.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Choanal Atresia / diagnosis
  • Comparative Genomic Hybridization
  • Empty Sella Syndrome / diagnosis*
  • Empty Sella Syndrome / genetics
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Leg Bones / abnormalities
  • Magnetic Resonance Imaging
  • Tomography, X-Ray Computed