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Updated: Jun 24, 2025

Multiplexed Fluorescent Immunohistochemical Staining, Imaging, and Analysis in Histological Samples of Lymphoma
Published on: January 9, 2019
Enhancing lymphoma diagnosis on core needle biopsies: Integrating immunohistochemistry with flow cytometry
Silvia Bellesi1, Gabriele Schiaffini2, Andrea Contegiacomo3
1Ematologia, Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Insights
Adding flow cytometry (FC) to image-guided core needle biopsies (IG-CNB) significantly improves lymphoma diagnosis accuracy. This approach enhances diagnostic rates and reduces the need for repeat excisional biopsies in suspected lymphoproliferative diseases.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Image-guided core needle biopsies (IG-CNB) are standard for lymphadenopathy but have diagnostic limitations.
- Lower efficacy compared to excisional biopsies necessitates improved diagnostic strategies.
Purpose of the Study:
- To evaluate the utility of incorporating flow cytometry (FC) with immunohistochemistry (IHC) in IG-CNB for suspected lymphoproliferative diseases.
- To assess the impact of FC on diagnostic accuracy and efficiency.
Main Methods:
- Analysis of 170 consecutive IG-CNB cases (ultrasound or CT-guided).
- Utilized a diagnostic algorithm with antibody cocktails for lymphoma identification.
- Compared diagnostic rates and failure rates with and without FC.
Main Results:
- FC expedited presumptive results in 87.6% of cases within 48 hours (98% PPV).
- Addition of FC to IHC increased diagnostic rate from 91.2% to 95.3%.
- FC reduced IG-CNB failure rate by 45% (from 8.8% to 4.7%), especially for deep-seated sites and recurrences.
Conclusions:
- Flow cytometry is a valuable adjunctive tool for IG-CNB in suspected lymphomas.
- FC improves diagnostic performance and has the potential to reduce repeat excisional biopsies.
- Quantification of surface markers by FC aids in targeted therapy selection.
Abstract:
Image-guided core needle biopsies (IG-CNB) represent a minimally invasive approach for obtaining tissue in patients with lymphadenopathy and suspected lymphoma. Despite their utility, diagnostic challenges persist, with lower efficacy compared with excisional biopsies. Our study aimed to evaluate the potential utility of incorporation of flow cytometry (FC) alongside immunohistochemistry (IHC) when performing IG-CNB for suspected lymphoproliferative diseases. Analyzing 170 consecutive cases, guided by ultrasound (n = 94) or computer tomography (n = 76), we employed a diagnostic algorithm, already established in our laboratory practice, utilizing three antibody cocktail-equipped tubes tailored for defining lymphomas, particularly those of B-cell origin. FC expedited the diagnostic process, yielding presumptive results in 87.6% of cases within 48 h, with a positive predictive value of 98%. Addition of FC to routine IHC enhanced the diagnostic rate from 91.2% to 95.3%, reducing IG-CNB failure rate by 45%, from 8.8% to 4.7%. This enhancement was particularly notable for deep-seated sites and in the setting of suspected disease recurrences. Consequently, FC emerges as a valuable adjunctive tool, allowing for the improvement of diagnostic performance, with a particular focus on the ability to quantify the expression of surface markers for targeted therapies, and holding the potential to diminish the necessity for repeat excisional biopsies subsequent to IG-CNB procedures.
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