Evidence map›Paper›PMID 41222195›Full record

ArticleTranslational vision science & technology2025

A Novel Manual "Centrifuged-Enhanced" Cytosmear Technique for Improving Hypocellular Cytology in the Diagnosis of Vitreoretinal Lymphoma.

Candice Ee Hua Ho, Thaddeus Luke Shen, Mona Meng Wang, Meihui Wu, Zhen Wei Neo, Felicia Wee, Joe Yeong, Anita Sook Yee Chan

Abstract read
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Article in Translational vision science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Candice Ee Hua HoTranslational Ophthalmic Pathology Platform, Singapore Eye Research Institute, Singapore, Singapore.
Thaddeus Luke ShenTranslational Ophthalmic Pathology Platform, Singapore Eye Research Institute, Singapore, Singapore.
Mona Meng WangTranslational Ophthalmic Pathology Platform, Singapore Eye Research Institute, Singapore, Singapore.
Meihui WuTranslational Ophthalmic Pathology Platform, Singapore Eye Research Institute, Singapore, Singapore.
Zhen Wei NeoInstitute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Felicia WeeInstitute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Joe YeongInstitute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Anita Sook Yee ChanTranslational Ophthalmic Pathology Platform, Singapore Eye Research Institute, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To develop a manual "centrifuged-enhanced cytosmear" technique for cytologic and immunohistochemical analysis of hypocellular vitreous biopsy specimens in vitreoretinal lymphoma (VRL). Methods: Diffuse large B-cell lymphoma cells were diluted to simulate vitreous biopsy yields (1000-50,000 cells/100 µL) and fixed in PreservCyt. Samples were centrifuged in a standard laboratory centrifuge and deposited into 1000 cells/100 µL PAP pen-defined circles on charged slides. Smears were air-dried, methanol-fixed, and stained with toluidine blue and CD20 immunohistochemistry (IHC). Cell density per high-power field (40×) was quantified and compared with noncentrifuged smears. Reproducibility was assessed across replicates and between two operators. Genomic DNA concentration was measured. Results: Centrifuged-enhanced cytosmears demonstrated significantly higher cellular densities than standard smears across all concentrations (P < 0.05), especially at 1000 to 2000 cells/100 µL, where standard smears failed to detect cells. CD20 IHC was successful without cell dropout. Genomic DNA yields ranged from 5.25 ng (1000 cells) to 143 ng (50,000 cells). Interuser variability was not significant. Comparison with cytospin clinical cases showed that centrifuged-enhanced cytosmears are of comparable cellularity to clinical cases. Conclusions: This centrifuged-enhanced cytosmear technique reliably concentrates sparse cells for cytology and IHC. It is reproducible and cost-effective, requiring no specialized equipment. Genomic DNA yields at very low cell counts of 1000 cells/100 µL is potentially sufficient for adjuvant MYD88 mutation analysis and can be used to support cytology diagnosis. Translational Relevance: The centrifuged-enhanced cytosmear offers an accessible alternative to cytospin preparations, enabling VRL diagnosis and IHC analysis in settings lacking cytology infrastructure or where cell blocks cannot be performed.

Indexed as

CytodiagnosisLymphoma, Large B-Cell, DiffuseRetinal NeoplasmsVitreous BodyAntigens, CD20BiopsyCentrifugationHumansImmunohistochemistryMyeloid Differentiation Factor 88Reproducibility of ResultsAntigens, CD20MYD88 protein, humanMyeloid Differentiation Factor 88

Identifiers

PMID41222195
PMCPMC12637000

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.