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DOI 10.1093/ajcp/aqae032

Медицинская библиотека · American journal of clinical pathology · 2024

Improving resource utilization: Axillary lymph node core biopsy triaging for lymphoma.

Dernell Carl, Astle John, Bogachkov Abraham, Reimer Shelly, Wadhwa Anubha, Majidi Shadie S, Canales Bethany, Jorns Julie M

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Аннотация

OBJECTIVES

To evaluate the utilization of hematopathology resources within our enterprise on axillary lymph node core biopsy (AxLNCB) specimens, particularly those obtained in the context of breast cancer screening.

METHODS

The utilization of hematopathology resources was determined for all AxLNCB specimens over a 30-month period from across our enterprise, and chart review was performed for select patient demographics and radiographic features. The AxLNCB cases with benign histology were reviewed for subtyping of histologic patterns.

RESULTS

Of the total 594 AxLNCB specimens, 61.6% were benign and 38.6% malignant. Of malignant cases, only 9.3% contained any hematologic malignancy, yet 94% of all cases received tissue triage for lymphoma, and 81% were reviewed at least in part by a hematopathologist. Six clinical parameters were found to independently predict risk of hematologic malignancy: male sex (P = .041), bilateral lymphadenopathy (P = .004), diffuse cortical thickening (P = .005), lack of breast cancer (P = .001), older age (P < .001), and history of hematologic malignancy (P < .001).

CONCLUSIONS

Our enterprise overused hematopathology resources in the evaluation of AxLNCB performed in the study period. Our process could improve from the application of a simple tool generated from this cohort to predict percent risk of the specimen containing hematologic malignancy using patient characteristics easily found via routine chart review.

Для цитирования: Dernell Carl, Astle John, Bogachkov Abraham, Reimer Shelly, Wadhwa Anubha, Majidi Shadie S, Canales Bethany, Jorns Julie M. Improving resource utilization: Axillary lymph node core biopsy triaging for lymphoma.. American journal of clinical pathology. 2024. DOI: 10.1093/ajcp/aqae032.

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