Paediatric Malignant Blue Cell Tumours- A Practical Pathological and Immunohistochemical Study in Duhok, Iraq
Introduction: Malignant Blue Cell Tumours (MBCTs) are common heterogeneous tumours among paediatric age group. Their heterogeneity is reflected in their therapeutic and prognostic diversity. Mere morphology is not enough to differentiate them. Immunohistochemistry is a key tool for identificatio...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Private Limited
2020-09-01
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Series: | Journal of Clinical and Diagnostic Research |
Subjects: | |
Online Access: | https://jcdr.net/articles/PDF/14055/44445_CE[Ra1]_F(SL)_PF1(AG_KM)_PFA(KM)_PB(AG_KM)_PN(SL).pdf |
Summary: | Introduction: Malignant Blue Cell Tumours (MBCTs) are common
heterogeneous tumours among paediatric age group. Their
heterogeneity is reflected in their therapeutic and prognostic
diversity. Mere morphology is not enough to differentiate them.
Immunohistochemistry is a key tool for identification of small
blue cell tumours that lack evidence of lineage differentiation on
the ground of light microscopic morphology.
Aim: To identify the immunohistochemical identity of paediatric
MBCTs in Duhok, Iraq.
Materials and Methods: This was a cross-sectional study
performed on 120 cancers reported morphologically as MBCTs
over 11-year period, from January 2009 to December 2019.
Clinical data and histomorphologic acumen were considered
and integrated with the immunohistochemical findings.
Applying autostainer, immunohistochemistry was performed
using monoclonal or polyclonal antibodies.
Results: Lymphoma/leukaemia topped the diagnostic list 36 (30%)
formed the commonest category, followed by Ewing’s/Primitive
Neuro Ectodermal Tumour (PNET) 29 (24.2%), Neuroblastoma 16
(13.3%), Wilm’s tumour 11 (9.2%), Rhabdomyosarcoma 9 (7.5%)
and Medulloblastoma 7 (5.8%). The remainders comprised
Retinoblastoma (3.4%), Glioblastoma and Ependymoma (2.5%
each). Hepatoblastoma and Astroblastoma formed the least
frequent tumours (0.8% each). These tumours were more frequently
located in the soft tissue (30%) followed by brain (14.2%), bone
(10%), Lymph Node (LN) (9.2%) and kidney (10%).
Conclusion: Integration of clinical data and histomorphologic
acumen helped much for categorisation of MBCTs. Application
of immunohistochemistry in this study has shown a significant
improvement in the diagnostic accuracy of paediatric MBCTs.
Loss of some differentiation antigens and aberrant expression of
some markers often necessitate the use of panels of antibodies
and, even molecular testing to target the task. |
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ISSN: | 2249-782X 0973-709X |