The utility of dynamic MRI in differentiating the hormone-producing ability of pituitary adenomas.
Dynamic contrast enhancement
Magnetic resonance imaging
Pituitary adenoma
Pituitary hormonal activity
Journal
Japanese journal of radiology
ISSN: 1867-108X
Titre abrégé: Jpn J Radiol
Pays: Japan
ID NLM: 101490689
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
received:
24
01
2021
accepted:
09
04
2021
pubmed:
22
4
2021
medline:
7
10
2021
entrez:
21
4
2021
Statut:
ppublish
Résumé
To investigate the relationship between dynamic magnetic resonance imaging (MRI) findings and hormonal activity in pituitary adenomas. We retrospectively evaluated the dynamic MRI findings in 244 patients with pathologically confirmed pituitary adenomas and a diagnosis of clinically active prolactin (PRL)-producing adenomas. Among the 244 pituitary adenomas, 55, 16, 6, and 4 produced growth hormone (GH), PRL, adrenocorticotropic hormone, and thyroid-stimulating hormone, respectively, while 163 were non-functioning (NF) adenomas. For each adenoma, we calculated the washout rate (WR) and early (EER) and delayed (DER) tumour-to-normal-tissue enhancement ratios. The respective mean values of the WR, EER, and DER were 9.4%, 75.2%, and 64.5% for GH-producing adenomas; 6.2%, 117.1%, and 106.2% for PRL-producing adenomas; and 5.4%, 116.7%, and 108.7% for NF adenomas. GH-producing adenomas had significantly lower EER and DER values than PRL-producing (P < 0.001) and NF adenomas (P < 0.001). In ROC analysis of GH-producing and non-GH-producing adenomas, the areas under the curves of WR, EER, and DER were 0.593, 0.825, and 0.857, respectively. There are differences in dynamic MRI features between GH-producing and non-GH-producing adenomas, which suggests that EER and DER may be useful for diagnosing GH-producing adenomas.
Identifiants
pubmed: 33881731
doi: 10.1007/s11604-021-01121-9
pii: 10.1007/s11604-021-01121-9
pmc: PMC8338864
doi:
Substances chimiques
Prolactin
9002-62-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
741-748Informations de copyright
© 2021. The Author(s).
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