Reference : Clinicopathologic and molecular analysis of a choroidal pigmented schwannoma in the c...
Scientific journals : Article
Human health sciences : Ophthalmology
http://hdl.handle.net/2268/113683
Clinicopathologic and molecular analysis of a choroidal pigmented schwannoma in the context of a PTEN hamartoma tumor syndrome.
English
Venturini, Giulia [> >]
Moulin, Alexandre P. [> >]
DEPREZ, Manuel [Centre Hospitalier Universitaire de Liège - CHU > > Anatomie pathologique >]
Uffer, Sylvie [> >]
Bottani, Armand [> >]
Zografos, Leonidas [> >]
Rivolta, Carlo [> >]
2012
Ophthalmology
Elsevier
119
4
857-64
Yes (verified by ORBi)
International
0161-6420
1549-4713
New York
NY
[en] Child ; Choroid Neoplasms/genetics/pathology/ultrasonography ; DNA Methylation ; DNA Mutational Analysis ; DNA, Neoplasm/genetics ; Eye Enucleation ; Female ; Hamartoma Syndrome, Multiple/genetics/pathology/ultrasonography ; Humans ; Immunohistochemistry ; Neurilemmoma/genetics/pathology/ultrasonography ; Neurofibromin 2/genetics ; PTEN Phosphohydrolase/genetics ; RNA, Messenger/genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Visual Acuity
[en] PURPOSE: To report the first case of choroidal schwannoma in a patient affected by PTEN hamartoma tumor syndrome (PHTS) and investigate the molecular involvement of the phosphatase and tensin homolog (PTEN) and neurofibromin 2 (NF2) genes in this rare intraocular tumor. DESIGN: Observational case report. PARTICIPANT: A 10-year-old girl diagnosed with PHTS. METHODS: The enucleated specimen underwent histologic, immunohistochemical, and transmission electronic microscopy. The expression of PTEN and NF2 and their protein products were evaluated by reverse transcription-polymerase chain reaction and immunohistochemistry. Somatic mutations of PTEN and NF2, as well as allelic loss, were investigated by direct sequencing of DNA extracted from the tumor. PTEN epigenetic silencing was investigated by pyrosequencing. MAIN OUTCOME MEASURES: Histopathologic and molecular characterization of a choroidal pigmented schwannoma. RESULTS: Histopathologic, immunohistochemical, and electron microscopic analysis demonstrated features consistent with a pigmented cellular schwannoma of the choroid. We found no loss of heterozygosity at the genomic level for the PTEN germline mutation and no promoter hypermethylation or other somatic intragenic mutations. However, we observed an approximate 40% reduction of PTEN expression at both the mRNA and the protein level, indicating that the tumor was nonetheless functionally deficient for PTEN. Although DNA sequencing of NF2 failed to identify any pathologic variants, its expression was abolished within the tumor. CONCLUSIONS: We report the first description of a pigmented choroidal schwannoma in the context of a PHTS. This rare tumor showed a unique combination of reduction of PTEN and absence of NF2 expression.
Researchers ; Professionals ; Students
http://hdl.handle.net/2268/113683
also: http://hdl.handle.net/2268/144191
10.1016/j.ophtha.2011.09.057
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Copyright (c) 2012 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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