Global Cytopathology-Hematopathology Practice Trends

Sara L Zadeh1, Ronald Balassanian2, Matthew C Cheung3

  • 1Department of Pathology, Stanford University, Stanford, CA, USA.

Insights

Small-volume biopsies for lymphoma diagnosis are common, but communication between hematopathology and cytopathology services is inconsistent. This lack of uniformity impacts diagnostic accuracy and patient management.

Area of Science:

  • Pathology
  • Hematology
  • Oncology

Background:

  • Small-volume biopsies, including fine-needle aspiration biopsy (FNAB) with or without core biopsy, are increasingly utilized for lymphoma diagnosis and management.
  • Effective integration of FNAB, core biopsy, and flow cytometry is crucial for accurate lymphoma diagnosis.

Purpose of the Study:

  • To survey current practices in small-volume biopsy diagnosis of lymphoma.
  • To assess the interaction between hematopathologists and cytopathologists.
  • To evaluate the integration of FNAB, core biopsy, and flow cytometry data during the sign-out process.

Main Methods:

  • A cross-sectional survey design was employed using the RedCap database.
  • The survey was distributed via email listservs of nine pathology professional societies.
  • 128 pathologists participated, answering 25 multiple-choice questions and free-text fields.

Main Results:

  • A majority of respondents (58.6%) encounter FNAB specimens for lymphoma diagnosis (FNAB-L) daily or weekly.
  • Most institutions (62.1%) have separate hematopathology and cytopathology services with inconsistent communication.
  • Identified barriers included poor communication, limited access to diagnostic studies, lack of subspecialty training, and differing opinions on FNAB for lymphoma diagnosis.

Conclusions:

  • FNAB-L specimens are frequently encountered in clinical practice.
  • There is a notable lack of uniformity in sharing complementary biopsy and flow cytometry data between hematopathology and cytopathology services.
  • Improved communication and standardized protocols are needed for optimal lymphoma diagnosis using small-volume biopsies.
Abstract