Literature DB >> 15587427

Spontaneous involution of a non-optic astrocytoma in neurofibromatosis type I: serial magnetic resonance imaging evaluation.

S Cakirer1, E Karaarslan.   

Abstract

A patient with neurofibromatosis type I (NF1) was followed-up with serial magnetic resonance imaging (MRI) studies over a period of 6 years. A contrast-enhancing lesion of the internal capsule, histologically proven to be pilocytic astrocytoma through stereotactic brain biopsy with mass effect and associated edema, was detected to reveal spontaneous involution on follow-up MRI studies. Although spontaneous regression of gliomas of the optic pathway-hypothalamus in patients with NF1 is relatively common in the literature, spontaneous involution of non-optic (i.e. areas other than optic pathways and hypothalamus) gliomas is rarely reported. Conservative management with follow-up MRI studies should be considered for non-optic glial tumors and tumor-like masses in patients with NF1, and surgical treatment should not be considered unless the lesions exhibit a rapid or unrelenting growth on serial MRI studies or produce significant clinical deterioration.

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Year:  2004        PMID: 15587427     DOI: 10.1080/02841850410001150

Source DB:  PubMed          Journal:  Acta Radiol        ISSN: 0284-1851            Impact factor:   1.990


  1 in total

1.  Regression of gadolinium-enhanced lesions in patients affected by neurofibromatosis type 1.

Authors:  Marta Lucchetta; Renzo Manara; Giorgio Perilongo; Maurizio Clementi; Eva Trevisson
Journal:  Radiol Med       Date:  2015-10-07       Impact factor: 3.469

  1 in total

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