Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Comparison of IDH and ATRX by immunohistochemistry with 1p/19q co-deletion by FISH in Oligodendrogliomas

View through CrossRef
Objective: To determine 1p/19q co-deletion by Fluorescence in situ hybridization (FISH) based on positive expression of IDH and ATRX by immunohistochemistry (IHC) in oligodendrogliomas. Study Design: Cross-sectional study. Place and Duration of Study: Department of Histopathology, Armed Forces Institute of Pathology, Rawalpindi Pakistan, from Oct 2021 to Jun 2022. Methodology: A total of 58 cases of oligodendrogliomas having positive expression of IDH and ATRX were subjected to FISH for 1p/19q co-deletion. FISH results were correlated with clinicopathological parameters and IHC by using computer software SPSS version 23. Results: In this study, age range is from 14 to 79 years, with mean of 40 years. 30(52%) cases are <40 years of age and 28(48%) cases are ≥40 years of age. There are 33(57%) males and 25(43%) females with a male to female ratio of 1.3:1. At the time of presentation, 25(43%) patients had headache, 19(33%) had focal neurological deficit, and 14(24%) had seizures. 1p/19q co-deletion by FISH was positive in 51(88%) specimens, whereas it was negative in 7(12%) specimens. 1p/19q co-deletion was not significantly associated with age, gender and clinical symptoms (p-value >0.05). Sensitivity & diagnostic accuracy of IHC with FISH as gold standard showed that combined sensitivity of IDH and ATRX was 100% with diagnostic accuracy of 87.93% for oligodendrogliomas. Conclusion: It’s concluded that oligodendrogliomas can be diagnosed with combined positive expression of IDH and ATRX with sensitivity of 100% and diagnostic accuracy of 87.93% where FISH for 1p/19q co-deletion is not available
Title: Comparison of IDH and ATRX by immunohistochemistry with 1p/19q co-deletion by FISH in Oligodendrogliomas
Description:
Objective: To determine 1p/19q co-deletion by Fluorescence in situ hybridization (FISH) based on positive expression of IDH and ATRX by immunohistochemistry (IHC) in oligodendrogliomas.
Study Design: Cross-sectional study.
Place and Duration of Study: Department of Histopathology, Armed Forces Institute of Pathology, Rawalpindi Pakistan, from Oct 2021 to Jun 2022.
Methodology: A total of 58 cases of oligodendrogliomas having positive expression of IDH and ATRX were subjected to FISH for 1p/19q co-deletion.
FISH results were correlated with clinicopathological parameters and IHC by using computer software SPSS version 23.
Results: In this study, age range is from 14 to 79 years, with mean of 40 years.
30(52%) cases are <40 years of age and 28(48%) cases are ≥40 years of age.
There are 33(57%) males and 25(43%) females with a male to female ratio of 1.
3:1.
At the time of presentation, 25(43%) patients had headache, 19(33%) had focal neurological deficit, and 14(24%) had seizures.
1p/19q co-deletion by FISH was positive in 51(88%) specimens, whereas it was negative in 7(12%) specimens.
1p/19q co-deletion was not significantly associated with age, gender and clinical symptoms (p-value >0.
05).
Sensitivity & diagnostic accuracy of IHC with FISH as gold standard showed that combined sensitivity of IDH and ATRX was 100% with diagnostic accuracy of 87.
93% for oligodendrogliomas.
Conclusion: It’s concluded that oligodendrogliomas can be diagnosed with combined positive expression of IDH and ATRX with sensitivity of 100% and diagnostic accuracy of 87.
93% where FISH for 1p/19q co-deletion is not available.

Related Results

Oligodendrogliomas: Critérios Histológicos e Moleculares
Oligodendrogliomas: Critérios Histológicos e Moleculares
Os oligodendrogliomas são tumores gliais primários do sistema nervoso central que acometem predominantemente adultos jovens e de meia-idade, localizando-se de forma preferencial no...
Abstract 345: Characterizing and therapeutically targeting G-quadruplex DNA in ATRX-mutant glioma
Abstract 345: Characterizing and therapeutically targeting G-quadruplex DNA in ATRX-mutant glioma
Abstract Inactivating ATRX mutations are defining molecular alterations in several cancer variants, including large subsets of malignant glioma. ATRX encodes a chrom...
CSIG-09. ATRX DEFICIENCY IN GLIOMA IMPACTS TRANSCRIPTIONAL PROFILES AND THE IMMUNE MICROENVIRONMENT IN VIVO
CSIG-09. ATRX DEFICIENCY IN GLIOMA IMPACTS TRANSCRIPTIONAL PROFILES AND THE IMMUNE MICROENVIRONMENT IN VIVO
Abstract Current treatment for diffuse astrocytoma fails to address its underlying molecular mechanisms leading to inevitable disease progression and eventual patien...
Rare dual‐genotype IDH mutant glioma: Review of previously reported cases and two new cases of true “oligoastrocytoma”
Rare dual‐genotype IDH mutant glioma: Review of previously reported cases and two new cases of true “oligoastrocytoma”
In 2016, the World Health Organization (WHO) eliminated “oligoastrocytoma” from the classification of central nervous system (CNS) tumors, in favor of an integrated histologic and ...
Sirtuin 2 inhibition modulates chromatin landscapes genome-wide to induce senescence in ATRX-deficient malignant glioma
Sirtuin 2 inhibition modulates chromatin landscapes genome-wide to induce senescence in ATRX-deficient malignant glioma
ABSTRACTInactivating mutations inATRXcharacterize large subgroups of malignant gliomas in adults and children. ATRX deficiency in glioma induces widespread chromatin remodeling, dr...
IMMU-10. EXPLORING THE IMMUNOLOGIC CONSEQUENCES OF ATRX DEFICIENCY IN GLIOMA
IMMU-10. EXPLORING THE IMMUNOLOGIC CONSEQUENCES OF ATRX DEFICIENCY IN GLIOMA
Abstract ATRX is a key chromatin regulator, which is mutated in large subsets of both adult and pediatric gliomas. Despite being a common mutation, little is known a...
Impact of D-2HG on the Tumor Microenvironment of IDH-mutated Gliomas
Impact of D-2HG on the Tumor Microenvironment of IDH-mutated Gliomas
Impact du D-2HydroxyGlutarate sur le micro-environnement tumoral des gliomes avec mutation IDH Contexte : Les gliomes diffus sont les tumeurs primitives malignes du...

Back to Top