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Multicenter Study
. 2023 Feb 1;47(2):212-217.
doi: 10.1097/PAS.0000000000001985. Epub 2022 Dec 20.

Diagnostic Discrepancies in Small-volume Biopsy for the Initial Diagnosis, Recurrence, and Transformation of Follicular Lymphoma: A Multi-Institutional Collaborative Study

Affiliations
Multicenter Study

Diagnostic Discrepancies in Small-volume Biopsy for the Initial Diagnosis, Recurrence, and Transformation of Follicular Lymphoma: A Multi-Institutional Collaborative Study

Ashley K Volaric et al. Am J Surg Pathol. .

Abstract

Small-volume biopsies (SVBs) including fine-needle aspiration (FNA), cell block, and needle core biopsies (NCB) are increasingly utilized to diagnose and guide the clinical management of lymphoma. We established a multi-institutional interdisciplinary collaboration of cytopathologists, hematopathologists, and oncologists focused on the role of SVB in the management of patients with follicular lymphoma (FL). To assess the performance characteristics of SVB in this setting, we evaluated all consecutive SVBs performed for clinical indications of initial diagnosis, recurrence, or transformation of FL over a 5-year period and focused on the 182 that had at least one subsequent biopsy within 3 months as part of the same clinical work-up. The most common outcome of a subsequent biopsy as part of the same clinical work-up was a more specific diagnosis usually assigning the pathologic grade (111/182, 61%), followed by a complete agreement with the SVB (24/182, 13%), and change from nondiagnostic on initial biopsy to diagnostic on subsequent biopsy (21/182, 12%). A minority resulted in a diagnostic change from benign to lymphoma (17/182, 9%), a change in FL grade (5/182, 3%), or change in the lymphoma diagnostic category (4/182, 2%). There were no cases where an initial diagnosis of lymphoma was overturned. The distribution of discrepancies was similar across initial SVB types (FNA, FNA + cell block, NCB with or without FNA). Tissue limitations were noted in a minority of cases (53/182, 29%) and were enriched among initially nondiagnostic biopsies (16/21, 76%). Flow cytometry immunophenotyping was performed in the majority of cases both at the first and last biopsy (147/182, 81%). SVB can be a powerful method to detect FL in various clinical indications, with discrepant cases mostly resulting from a refinement in the initial diagnosis.

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Conflict of interest statement

Conflicts of Interest and Source of Funding: The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article.

Figures

Figure 1.
Figure 1.
Biopsy Types at Initial and Final Biopsy, All Work-ups (n=182). N.B. Initial surgical biopsies (incisional or excisional) were excluded per study inclusion criteria. Numbers above each bar graph indicate absolute case numbers.
Figure 2.
Figure 2.
Diagnoses at Initial and Final SVB Biopsy, All Work-ups (n=182). N.B. Numbers above each bar graph indicate absolute case numbers NDA, Non-diagnostic; Limited, Limited Sample; Suspicious, Suspicious for Malignancy; Atypical, Atypical Cells Present; FL, unk, Follicular Lymphoma, Unknown Grade; FL, 1-2, Follicular Lymphoma, Grade 1-2; FL, 3A, Follicular Lymphoma, Grade 3A; FL, 3B, Follicular Lymphoma, Grade 3B; LBCL, Large B cell Lymphoma; DLBCL, Diffuse Large B cell Lymphoma; FL, ped type, Pediatric-Type Follicular Lymphoma; PCFCL, Primary Cutaneous Follicle Center Lymphoma; CHL, Classic Hodgkin Lymphoma; BCL, B cell Lymphoma
Figure 3.
Figure 3.
Flow Cytometry Performed at Initial and Final Diagnosis per Diagnostic Discrepancy Category, All Work-ups (n= 182). N.B. Numbers above each bar graph indicate absolute case numbers. B to M, Benign to Malignant; ND to Dx, Non-Diagnostic to Diagnostic

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