Pericallosal lipoma extending through the choroidal fissure: US/CT/MRI correlation

1992 ◽  
Vol 34 (5) ◽  
pp. 402-403 ◽  
Author(s):  
G. I. Melin ◽  
M. S. Keller
Keyword(s):  
Pericallosal Lipoma

scholarly journals Pericallosal lipoma in an infant with fetal alcohol syndrome: a case report

2021 ◽  
Vol 16 (3) ◽  
pp. 75-78
Author(s):  
G. S. Golosnaya ◽  
M. Yu. Novikov ◽  
N. Yu. Knyazeva ◽  
D. Yu. Volodina ◽  
A. A. Skobeltsyn ◽  
...  
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Fetal Alcohol Syndrome ◽  
Intrauterine Infection ◽  
Brain Malformation ◽  
Fetal Alcohol ◽  
Perinatal Center ◽  
Pericallosal Lipoma

In this article we report a case of pericallosal lipoma in a newborn with fetal alcohol syndrome, brain malformation (agenesis of the corpus callosum), and intrauterine infection (meningitis) diagnosed in a perinatal center.

Giant pericallosal lipoma presenting with psychosis

2018 ◽  
Vol 66 (2) ◽  
pp. 553
Author(s):  
Yaxiong Li ◽  
Xin Wang ◽  
Fengshi Fan
Keyword(s):  
Pericallosal Lipoma

scholarly journals A Rare Case of Pericallosal Lipoma Associated with Bilaterally Symmetrical Lateral Ventricular Choroid Plexus Lipomas without Corpus Callosal Anomalies

2013 ◽  
Vol 3 ◽  
pp. 69 ◽  
Author(s):  
Parag Suresh Mahajan ◽  
Nawal M. Al Moosawi ◽  
Islam Ali Hasan
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Brain Tumors ◽  
Corpus Callosum ◽  
Choroid Plexus ◽  
Rare Case ◽  
Rare Presentation ◽  
Pericallosal Lipoma ◽  
Central Nervous System Anomalies

Lipomas constitute less than 5% of primary brain tumors. Pericallosal lipomas (PCLp) constitute almost half of all intracranial lipomas. Corpus callosal anomalies commonly occur in cases with PCLps. Although PCLp is often described as corpus callosal lipoma, it is most often pericallosal in location. PCLps may have calcification in the periphery and may continue into lateral ventricles, which is a very rare presentation. We observed a case of PCLp with peripheral calcifications associated with PCLp continuing as bilaterally symmetrical lateral ventricular choroid plexus lipomas (CPLp) without any corpus callosal or other central nervous system anomalies, and as this is not been previously reported, we are presenting it. The appearance of PCLp in this case does not correspond to the descriptions of any of the existing morphological types (anterior and posterior) of classification of PCLps; it is rather mixed, where PCLp occupies both anterior and posterior locations around the corpus callosum.

Pai Syndrome: An Adult Patient with Bifid Nose and Frontal Hairline Marker

2003 ◽  
Vol 40 (3) ◽  
pp. 325-328 ◽  
Author(s):  
Y. Kenan Coban ◽  
Cetin Boran ◽  
S. Alp Omeroglu ◽  
Erdogan Okur
Keyword(s):  
Magnetic Resonance Imaging ◽  
Mental Retardation ◽  
Magnetic Resonance ◽  
Adult Patient ◽  
Normal Male ◽  
Resonance Imaging ◽  
Upper Lip ◽  
Chromosomal Study ◽  
Median Cleft ◽  
Pericallosal Lipoma

Objective A 17-year-old previously unreported patient with Pai syndrome is described. The boy had median cleft of upper lip, a polypoid skin mass over the columella, a minimal cleft of the upper central incisors, frontal alopecia of the anterior hairline, and bifid nose. Magnetic resonance imaging showed pericallosal lipoma. No mental retardation was present, and a chromosomal study showed normal male 46, XY karyotype.

scholarly journals A pericallosal lipoma case with evidence of surface dyslexia

Cortex ◽  
2019 ◽  
Vol 117 ◽  
pp. 414-416 ◽  
Author(s):  
Mark A. Eckert ◽  
Kenneth I. Vaden ◽  
Donna R. Roberts ◽  
Anne Castles
Keyword(s):  
Pericallosal Lipoma ◽  
Surface Dyslexia
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