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Comparison of risk of malignancy in a subgroup with atypia of undetermined significance/follicular lesion of undetermined significance: A meta-analysis. | LitMetric

Comparison of risk of malignancy in a subgroup with atypia of undetermined significance/follicular lesion of undetermined significance: A meta-analysis.

Head Neck

Department of Otorhinolaryngology Head Neck Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, South Korea.

Published: August 2017

AI Article Synopsis

  • The study identifies varying risks of cancer in different subgroups of atypia, particularly focusing on the categories of AUS/FLUS.
  • A meta-analysis of existing literature revealed that the cellular atypia group had a significantly higher risk of malignancy that was distinct from the other subgroups.
  • It concludes that cytologic atypia poses a notably greater risk than architectural atypia, suggesting it should be categorized separately for better risk assessment.

Article Abstract

Background: As heterogeneous findings are included in the atypia of undetermined significance (AUS)/follicular lesion of undetermined significance (FLUS) category, differing risks of malignancy in subgroups have been reported in several articles.

Methods: We performed a meta-analysis of full-text publications written in English found in the Embase and PubMed databases.

Results: The 4-tiered subgroup proportion meta-analysis showed that the 95% confidence interval (95% CI) of the risk of malignancy in the cellular atypia group did not overlap with the other 3 subgroups and demonstrated a significant difference. Two-tiered analysis using the cytologic and architectural atypia groups showed that cytologic atypia group had a 2.64-fold increase in the risk of malignancy compared with the architectural atypia group.

Conclusion: The cytologic atypia had a significantly higher risk of malignancy than the architectural atypia group, and it should be considered as a separate category.

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Source
http://dx.doi.org/10.1002/hed.24768DOI Listing

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