Literature DB >> 7955666

Oligodendroglial hamartoma of the right temporal lobe: a case report and discussion of possible histogenesis.

E Tasdemiroglu1, M Nazek, M Zuccarello.   

Abstract

A case of oligodendroglial hamartoma is reported in a 39-year-old man with a 20-year history of petit mal seizures. Magnetic Resonance Imaging of the brain showed a small focal area of abnormal decreased signal on T1-weighted images of the right temporal lobe. The patient became seizure free after the removal of the lesion and treatment with carbamazepine. Pathologic examination revealed several aggregates of oligodendroglial cells with small, dark, regularly stained nuclei and a clear, well-defined perinuclear halo; there was no mixture of neurons or astrocytes. Although these cells were negative, the background was strongly positive for glial fibrillary acidic protein, and myelin basic protein. The histopathologic diagnosis of the temporal lobe lesion was oligodendroglial hamartoma. This report documents an additional subtype of temporal lobe hamartoma associated with seizure disorder.

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Year:  1994        PMID: 7955666

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN: 0722-5091            Impact factor:   1.368


  2 in total

1.  Oligodendroglial hamartoma: a potential source of misdiagnosis for oligodendroglioma.

Authors:  Gianluca Marucci; Marco Giulioni; Matteo Martinoni; Lilia Volpi; Roberto Michelucci
Journal:  J Neurooncol       Date:  2010-06-08       Impact factor: 4.130

2.  Bilateral oligodendroglial hamartomas: A rare cause of drug-resistant epilepsy in a pediatric patient.

Authors:  Havisha Munjal; Devanshi Mistry; Jeevak Almast; Shehanaz Ellika
Journal:  J Clin Imaging Sci       Date:  2022-05-05
  2 in total

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