Purpose: Multinodular and vacuolating neuronal tumor (MVNT) is a rarely diagnosed neoplastic lesion often associated with adult-onset focal seizures. In some situations, atypical MRI features of MVNT may mimic other long-term epilepsy associated tumors (LEATs) or diffuse low-grade gliomas. In such a context, the identification of distinct clinical markers is recommended.
Methods: We retrospectively analyzed the neuroimaging features of histologically confirmed MVNT lesions of our epilepsy surgery cohort. All the identified MVNT patients had a mesial temporal lobe location. The MRI features from the MVNT population were compared to those from non-MVNT lesions randomly selected in our cohort. Non-MVNT lesions consisted of (i) other tumoral lesions belonging to LEATs group, (ii) infiltrative tumoral lesions such as grade 2, IDH-mutant Gliomas, and (iii) non-tumoral, highly epileptogenic lesions, such as hippocampal sclerosis.
Results: MRI analysis of patients with MVNT noticed an unusual FLAIR hyperintense signal extending from the uncus to the anterior white commissure through the sublenticular region. This neuroimaging abnormality visually mimicked "Mickey Mouse's hand" on coronal plane. The "Mickey Mouse's hand" sign was identified in 6 patients out of 9 (66.7%) MVNT patients. We did not identify the Mickey Mouse's hand sign in other control lesions (0/11 ganglioglioma, 0/11 glioma, 0/150 hippocampal sclerosis), except in one patient with dysembryoplastic neuroepithelial tumors (DNET) (1/15; 6.7%). All patients showing the "Mickey Mouse's hand" sign were seizure-free after surgery.
Conclusions: The Mickey Mouse's hand sign represents a straightforward and easy-to-remember neuroimaging feature, that does not require advanced MRI sequences and that could help clinicians facing mesial temporal lesions to rapidly raise the suspicion of MVNT diagnosis.
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http://dx.doi.org/10.1007/s11060-025-04962-w | DOI Listing |
J Neurooncol
March 2025
Epilepsy and EEG Unit, Department of Neurology, Pitié-Salpêtrière Hospital, Reference Center for Rare Epilepsies, ERN-EPICARE, AP-HP, 75013, Paris, France.
Purpose: Multinodular and vacuolating neuronal tumor (MVNT) is a rarely diagnosed neoplastic lesion often associated with adult-onset focal seizures. In some situations, atypical MRI features of MVNT may mimic other long-term epilepsy associated tumors (LEATs) or diffuse low-grade gliomas. In such a context, the identification of distinct clinical markers is recommended.
View Article and Find Full Text PDFCureus
October 2024
Department of Medicine, College of Medicine and Health Sciences, An-Najah National University, Nablus, PSE.
This article represents a unique CT-based sign called the Mickey Mouse sign in a diabetic female who presented with abdominal distension and mixed urinary symptoms. The CT scan showed that the bladder was massively dilated but compliant without impacting the upper urinary tract. The subtle clinical presentation and the impressive CT scan findings encouraged us to report this case as underactive bladder syndrome (UAB) is underreported and underinvestigated.
View Article and Find Full Text PDFJ Speech Lang Hear Res
January 2025
Department of Otolaryngology, Hannover Medical School, Germany.
J Neurochem
September 2024
Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine & Health, University of Sydney, Camperdown, New South Wales, Australia.
Sanfilippo syndrome results from inherited mutations in genes encoding lysosomal enzymes that catabolise heparan sulfate (HS), leading to early childhood-onset neurodegeneration. This study explores the therapeutic potential of photobiomodulation (PBM), which is neuroprotective and anti-inflammatory in several neurodegenerative diseases; it is also safe and PBM devices are readily available. We investigated the effects of 10-14 days transcranial PBM at 670 nm (2 or 4 J/cm/day) or 904 nm (4 J/cm/day) in young (3 weeks) and older (15 weeks) Sanfilippo or mucopolysaccharidosis type IIIA (MPS IIIA) mice.
View Article and Find Full Text PDFClin Nucl Med
June 2024
From the Nuclear Medicine Unit, Department of Radiology and Nuclear Medicine, Tuen Mun Hospital, Hong Kong.
Progressive supranuclear palsy (PSP) is the most prevalent form of degenerative atypical parkinsonism. Clinical manifestations of PSP commonly encompass deficits in vertical gaze, postural stability, akinesia, and cognitive impairment. The characteristic metabolic pattern observed in PSP through FDG PET displays hypometabolism in the midbrain, striatum, thalamus, and frontal lobe.
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