Literature DB >> 10206167

Spontaneous remission of chiasmatic/hypothalamic masses in neurofibromatosis type 1: report of two cases.

S Gottschalk1, R Tavakolian, A Buske, S Tinschert, R Lehmann.   

Abstract

We report two children with neurofibromatosis type 1 showing enhancing masses on MRI suggesting neoplasms in the chiasm and hypothalamic region. In both patients no visual or endocrinal dysfunction was present. On serial MRI spontaneous partial remission was found, implying that a cautious approach to therapeutic management of similar cases should be taken.

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Mesh：

Year:  1999        PMID： 10206167     DOI： 10.1007/s002340050734

Source DB:  PubMed          Journal:  Neuroradiology        ISSN： 0028-3940            Impact factor:   2.804


  12 in total

Review 1.  Spontaneous regression of optic pathways gliomas in three patients with neurofibromatosis type I and critical review of the literature.

Authors:  Manolo Piccirilli; Jacopo Lenzi; Catia Delfinis; Guido Trasimeni; Maurizio Salvati; Antonino Raco
Journal:  Childs Nerv Syst       Date:  2006-04-26       Impact factor: 1.475

2.  Spontaneous regression of cerebellar astrocytoma after subtotal resection.

Authors:  Paul Steinbok; Ken Poskitt; Glenda Hendson
Journal:  Childs Nerv Syst       Date:  2006-03-16       Impact factor: 1.475

Review 3.  Optic Pathway Gliomas in Neurofibromatosis Type 1: An Update: Surveillance, Treatment Indications, and Biomarkers of Vision.

Authors:  Peter M K de Blank; Michael J Fisher; Grant T Liu; David H Gutmann; Robert Listernick; Rosalie E Ferner; Robert A Avery
Journal:  J Neuroophthalmol       Date:  2017-09       Impact factor: 3.042

4.  Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children.

Authors:  Roxana S Gunny; Richard D Hayward; Kim P Phipps; Brian N Harding; Dawn E Saunders
Journal:  Pediatr Radiol       Date:  2005-07-27

5.  Magnetic resonance diffusion tensor imaging (MRDTI) of the optic nerve and optic radiations at 3T in children with neurofibromatosis type I (NF-1).

Authors:  Christopher G Filippi; Aaron Bos; Joshua P Nickerson; Michael B Salmela; Chris J Koski; Keith A Cauley
Journal:  Pediatr Radiol       Date:  2011-08-21

6.  Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1.

Authors:  Eva Trevisson; Matteo Cassina; Enrico Opocher; Virginia Vicenzi; Marta Lucchetta; Raffaele Parrozzani; Giacomo Miglionico; Rodica Mardari; Elisabetta Viscardi; Edoardo Midena; Maurizio Clementi
Journal:  J Neurooncol       Date:  2017-06-02       Impact factor: 4.130

7.  Remission of a chiasmatic glioma in a non-NF1 patient after brief chemotherapy with vincristine and carboplatin: case report and literature review.

Authors:  Elpis Mantadakis; Maria Raissaki; Vassiliki Danilatou; Alexander Kambourakis; Eftichia Stiakaki; Maria Kalmanti
Journal:  J Neurooncol       Date:  2004 Mar-Apr       Impact factor: 4.130

Review 8.  Neurofibromatosis type 1 and associated malignancies.

Authors:  Kaleb Yohay
Journal:  Curr Neurol Neurosci Rep       Date:  2009-05       Impact factor: 5.081

9.  Correlation of optical coherence tomography parameters with clinical and radiological progression in patients with symptomatic optic pathway gliomas.

Authors:  Masoud Aghsaei Fard; Sara Fakhree; Bahram Eshraghi
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2013-06-05       Impact factor: 3.117

Review 10.  Spontaneous complete regression of hypothalamic pilocytic astrocytoma after partial resection in a child, complicated with Stevens-Johnson syndrome: a case report and literature review.

Authors:  Mohammad Samadian; Mehrdad Hosseinzadeh Bakhtevari; Karim Haddadian; Hossein Afshin Alavi; Omidvar Rezaei
Journal:  Neurosurg Rev       Date:  2015-12-14       Impact factor: 3.042
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