Bright rim sign (DNET)
Citation, DOI, disclosures and article data
At the time the article was created Frank Gaillard had no recorded disclosures.
View Frank Gaillard's current disclosuresAt the time the article was last revised Joshua Yap had no financial relationships to ineligible companies to disclose.
View Joshua Yap's current disclosures- Bright rim sign - DNET
- Hyperintense rim sign in DNET
- Hyperintense rim sign in dysembryoplastic neuroepithelial tumours
The bright rim sign, also known as the hyperintense ring sign, has been described in dysembryoplastic neuroepithelial tumors (DNET). It is described as a well-defined rim of high signal around the DNET on FLAIR sequences. This T2/FLAIR hyperintense ring, whether complete or incomplete, is fairly sensitive and specific for DNET 2. On postoperative imaging, this sign may be a helpful clue for residual tumor or tumor recurrence 2.
On pathologic examination, this bright rim sign corresponds to glioneural elements loosely packed at the margin of the tumor 1.
This sign can, however, be very difficult to distinguish from the T2/FLAIR mismatch sign seen in astrocytomas, IDH-mutant.
Quiz questions
References
- 1. Raz E, Kapilamoorthy TR, Gupta AK et-al. Case 186: Dysembrioplastic neuroepithelial tumor. (2012) Radiology. 265 (1): 317-20. doi:10.1148/radiol.12100118 - Pubmed
- 2. Parmar HA, Hawkins C, Ozelame R et-al. Fluid-attenuated inversion recovery ring sign as a marker of dysembryoplastic neuroepithelial tumors. (2007) Journal of computer assisted tomography. 31 (3): 348-53. doi:10.1097/01.rct.0000243453.33610.9d - Pubmed
Related articles: Malformations of the central nervous system
-
malformations of cortical development
- abnormal cell proliferation or apoptosis
- abnormal brain size
-
microcephaly
- with normal to simplified cortical pattern
- microcephaly with lissencephaly
- microcephaly with extensive polymicrogyria
- macrocephalies (megalencephaly/macrocephaly)
-
microcephaly
- abnormal cell proliferation
- non-neoplastic
- cortical hamartomas of tuberous sclerosis
- hemimegalencephaly
-
focal cortical dysplasia (Type I and Type IIb)
- Palmini classification (2004)
- Barkovich classification (2005)
- Blumcke classification (2011)
- neoplastic
- non-neoplastic
- abnormal neuronal migration
- lissencephaly
- lissencephaly type I: subcortical band heterotopia spectrum (band heterotopia): undermigration
- lissencephaly type II (cobblestone complex)
- heterotopia: ectopic migration
- subependymal heterotopia
- subcortical heterotopia (not including band heterotopia)
- marginal glioneuronal heterotopia
- lissencephaly
- abnormal cortical organization
- mild malformations of cortical development (previously microdysgenesis)
-
polymicrogyria and schizencephaly
- bilateral polymicrogyria syndromes
- schizencephaly
- focal cortical dysplasia (Type IIa)
- abnormal brain size
- not otherwise classified
- malformations secondary to inborn errors of metabolism
- mitochondrial and pyruvate metabolic disorders
- peroxisomal disorders
- other unclassified malformations
- malformations secondary to inborn errors of metabolism
- abnormal cell proliferation or apoptosis
-
midline abnormalities of the brain
- absent septum pellucidum
- cephaloceles
-
midline nasal region lesions
- nasal dermoid
- nasal glioma
- nasal dermal sinus
- cerebral hemispheres
-
holoprosencephaly/septo-optic dysplasia spectrum
- septo-optic dysplasia
- lobar holoprosencephaly
- semilobar holoprosencephaly
- alobar holoprosencephaly
- middle interhemispheric variant/syntelencephaly
-
holoprosencephaly/septo-optic dysplasia spectrum
- corpus callosum
- intracranial lipoma
-
malformations of the cerebellum
- cerebellar hypoplasia
- focal hypoplasia
- generalized hypoplasia
- with enlarged fourth ventricle
- normal fourth ventricle
- with normal pons
- with small pons
- normal foliation
- pontocerebellar hypoplasias of Barth, types I and II
- cerebellar hypoplasias, not otherwise specified
- normal foliation
- cerebellar dysplasia
- focal dysplasia
- isolated vermian dysplasia
- molar tooth malformations including Joubert syndrome
- rhombencephalosynapsis
- isolated hemispheric dysplasia
- focal cerebellar cortical dysplasias/heterotopia
- dysplastic cerebellar gangliocytoma
- isolated vermian dysplasia
- generalized dysplasia
- congenital muscular dystrophies
- cytomegalovirus
- lissencephaly with RELN mutation
- lissencephaly with agenesis of corpus callosum and cerebellar dysplasia
- associated with diffuse cerebral polymicrogyria
- diffusely abnormal foliation
- focal dysplasia
- cerebellar hypoplasia
- malformations of the brainstem