Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis

MUTLU, H; PAKER, B; GUNES, N; EMEKTAR, A; KECELI, M; Kantarcı, Abdulmecit

doi:10.1007/s00234-004-1296-x

Makale Tam Makale Uluslararası 2004

Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis

H MUTLU, B PAKER, N GUNES, A EMEKTAR, M KECELI, Abdulmecit Kantarcı

NEURORADIOLOGY Cilt 46 · Sayı 12 · ss. 1036–1038 · 01.12.2004

DOI ile aç

Özet

We report a case of pituitary duplication in a neonate girl whose magnetic resonance (MR) images showed unusual findings of hypogenesis of the corpus callosum and oral dermoid. Pituitary duplication is an extremely rare malformation, with only a few previously reported cases. It occurs most commonly in association with complicated midline and skull base anomalies. We present a case of this malformation with special emphasis on the hypogenesis of splenium of the corpus callosum and oral dermoid.

Anahtar kelimeler

Magnetic resonance imaging GLAND pituitary duplication hypogenesis of corpus callosum

Atıf için künye

MUTLU, H., PAKER, B., GUNES, N., EMEKTAR, A., KECELI, M., & Kantarcı, A. (2004). Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis. NEURORADIOLOGY, 46(12), 1036–1038. https://doi.org/10.1007/s00234-004-1296-x

BibTeX

@article{mutlu2004-230245,
  author = {MUTLU, H and PAKER, B and GUNES, N and EMEKTAR, A and KECELI, M and Kantarcı, Abdulmecit},
  title = {Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis},
  journal = {NEURORADIOLOGY},
  year = {2004},
  volume = {46},
  number = {12},
  pages = {1036--1038},
  issn = {0028-3940},
  doi = {10.1007/s00234-004-1296-x},
  url = {https://akademik.atauni.edu.tr/yayinlar/230245-pituitary-duplication-associated-with-oral-dermoid-and-corpus-callosum}
}