𝔖 Bobbio Scriptorium
✦   LIBER   ✦

NMR imaging of congenital intracranial germinal layer neoplasms

✍ Scribed by H. D. Davidson; T. Ouchi; R. E. Steiner

Publisher
Springer
Year
1985
Tongue
English
Weight
286 KB
Volume
27
Category
Article
ISSN
0028-3940

No coin nor oath required. For personal study only.

✦ Synopsis

NMR images in five patients with surgically proved, congenital germinal layer intracranial neoplasms (two dermoid and three epidermoid tumors) were reviewed. The dermoids were typically midline (suprasellar or parapineal) masses with sharply-defined margins. Relaxation times were variable, but if fat was present, T1 was decreased, and T2 was increased. The epidermoids were off the midline (cerebellopontine angle, temporal lobe, frontal lobe) masses with generally long T1 and T2 relaxation times. Obstructive hydrocephaly was noted in one patient, and tumor to ventricular communication was demonstrated in another.

πŸ“œ SIMILAR VOLUMES

High-dose gadoteridol in MR imaging of i
High-dose gadoteridol in MR imaging of intracranial neoplasms
✍ Val M. Runge; John E. Kirsch; Vickie J. Burke; Ann C. Price; Kevin L. Nelson; Gr πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 964 KB

## Abstract Twelve patients with a high suspicion of brain metastases by previous clinical or radiologic examinations were studied in a phase III investigation with magnetic resonance (MR) imaging at 1.5 T after a bolus intravenous injection of 0.1 mmol/kg gadoteridol followed at 30 minutes by a se

Detection of metabolic heterogeneity of
Detection of metabolic heterogeneity of human intracranial tumors in vivo by 1h nmr spectroscopic imaging
✍ Christoph M. Segebarth; Danielle F. BalΓ©riaux; Peter R. Luyten; Jan A. Den Holla πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 855 KB

## Abstract Patients with intracranial tumors (gliomas) were examined by means of localized water‐suppressed ^1^H NMR single volume spectroscopy and spectroscopic imaging. The ^1^H NMR spectra of the tumors exhibit signal intensities of the N‐acetyl aspartate, choline compounds, and creatine plus p