Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation
Background: Chordoid Meningioma is a rare brain tumour characterized genetically by loss of genetic material from chromosome 22q at cytogenetic level resulting in mutation of NF2 gene. Objectives and case report: In the present report, we described a rare case of suprasellar chordoid meningioma,...
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| Format: | Article |
| Language: | English |
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Knowledge E
2017-09-01
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| Series: | Sudan Journal of Medical Sciences |
| Online Access: | https://knepublishing.com/index.php/SJMS/article/view/1001 |
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| author | Imad Fadl-Elmula Rania Giha Sawsan AH Deaf Lamyaa Ahmed El Hassan Ahmed M. Hassan Mohamed AR Arbab |
| author_facet | Imad Fadl-Elmula Rania Giha Sawsan AH Deaf Lamyaa Ahmed El Hassan Ahmed M. Hassan Mohamed AR Arbab |
| author_sort | Imad Fadl-Elmula |
| collection | DOAJ |
| description | Background: Chordoid Meningioma is a rare brain tumour characterized genetically by loss of genetic material from chromosome 22q at cytogenetic level resulting in mutation of NF2 gene.
Objectives and case report: In the present report, we described a rare case of suprasellar chordoid meningioma, which presented in a 32-year-old-woman. Her only complain was throbbing headache. Neurological examination showed left temporal hemianopia, decreased visual acuity (3/6), and no physical abnormalities related to Castleman syndrome were noted. Cranial magnetic resonance (MR) images demonstrated a 28x15 mm mass in the sellar region, which showed iso-to low intensity that enhanced vividly after gadolinium with upwards displacement of the Optic chiasm.
Total surgical excision of the tumour was performed and subsequent histological examination of the tumour showed typical histology pattern of chordoid meningioma grade II according to the WHO classification system of meningiomas.
Genomic DNA was extracted and mutation analysis for INI1 gene using primer of exon 4, 5, 7, and 9 showed mutation involving exon 9. DNA sequencing showedheterozygosity C-T mutation in exon 9 of INI1 gene leading to change of amino acid serine to phenylalanine at (codon 63). The details of this case are presented with a review of the literature. |
| format | Article |
| id | doaj-art-d58d1cdd803147818263bc397bcd5450 |
| institution | Kabale University |
| issn | 1858-5051 |
| language | English |
| publishDate | 2017-09-01 |
| publisher | Knowledge E |
| record_format | Article |
| series | Sudan Journal of Medical Sciences |
| spelling | doaj-art-d58d1cdd803147818263bc397bcd54502025-01-24T11:20:02ZengKnowledge ESudan Journal of Medical Sciences1858-50512017-09-0112319820610.18502/sjms.v12i3.10011001Rare Suprasellar Chordoid Meningioma with INI1 Gene MutationImad Fadl-ElmulaRania GihaSawsan AH DeafLamyaa Ahmed El HassanAhmed M. HassanMohamed AR ArbabBackground: Chordoid Meningioma is a rare brain tumour characterized genetically by loss of genetic material from chromosome 22q at cytogenetic level resulting in mutation of NF2 gene. Objectives and case report: In the present report, we described a rare case of suprasellar chordoid meningioma, which presented in a 32-year-old-woman. Her only complain was throbbing headache. Neurological examination showed left temporal hemianopia, decreased visual acuity (3/6), and no physical abnormalities related to Castleman syndrome were noted. Cranial magnetic resonance (MR) images demonstrated a 28x15 mm mass in the sellar region, which showed iso-to low intensity that enhanced vividly after gadolinium with upwards displacement of the Optic chiasm. Total surgical excision of the tumour was performed and subsequent histological examination of the tumour showed typical histology pattern of chordoid meningioma grade II according to the WHO classification system of meningiomas. Genomic DNA was extracted and mutation analysis for INI1 gene using primer of exon 4, 5, 7, and 9 showed mutation involving exon 9. DNA sequencing showedheterozygosity C-T mutation in exon 9 of INI1 gene leading to change of amino acid serine to phenylalanine at (codon 63). The details of this case are presented with a review of the literature.https://knepublishing.com/index.php/SJMS/article/view/1001 |
| spellingShingle | Imad Fadl-Elmula Rania Giha Sawsan AH Deaf Lamyaa Ahmed El Hassan Ahmed M. Hassan Mohamed AR Arbab Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation Sudan Journal of Medical Sciences |
| title | Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation |
| title_full | Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation |
| title_fullStr | Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation |
| title_full_unstemmed | Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation |
| title_short | Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation |
| title_sort | rare suprasellar chordoid meningioma with ini1 gene mutation |
| url | https://knepublishing.com/index.php/SJMS/article/view/1001 |
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