<p>Bronchoalveolar lavage fluid (BALF) cytology provides an important basis for the diagnosis and treatment of lung diseases. Current cytological analysis of BALF relies on manual microscopic examination, which is time-consuming, laborious, and experience-dependent. Automated identification of BALF cytology helps increase the accuracy and speed of screening qualified samples and subsequent cytomorphology analysis. However, there is a lack of public clinical BALF cell datasets for the detection of different cell types and a lack of pixel-level annotations for cytomorphology analysis. In this work, high-resolution cell images from clinical bronchoalveolar lavage sample obtained at the Chinese PLA General Hospital from 2018–2024 were collected, and pixel-level high-quality instance annotations of seven cell types were labeled. In total, 2,105 clinical images were gathered, with 13,263 cells from seven distinct classes, via both contour fine labeling and bounding box labeling. The dataset was trained and tested by the YOLOv8 instance segmentation network. The results demonstrated that the dataset and model we provided are beneficial for the study of automated cell identification in BALF.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

PW-BALFC, a clinical dataset for detection and instance segmentation of bronchoalveolar lavage fluid cell

  • Xin Shi,
  • Qing Huang,
  • Teng Xu,
  • Hongwen Mei,
  • Tingwei Quan,
  • Xiuli Wang,
  • Yinghan Shi,
  • Ye Hu,
  • Zhimei Duan,
  • Fei Xie,
  • Sifan Li,
  • Lixin Xie,
  • Kaifei Wang

摘要

Bronchoalveolar lavage fluid (BALF) cytology provides an important basis for the diagnosis and treatment of lung diseases. Current cytological analysis of BALF relies on manual microscopic examination, which is time-consuming, laborious, and experience-dependent. Automated identification of BALF cytology helps increase the accuracy and speed of screening qualified samples and subsequent cytomorphology analysis. However, there is a lack of public clinical BALF cell datasets for the detection of different cell types and a lack of pixel-level annotations for cytomorphology analysis. In this work, high-resolution cell images from clinical bronchoalveolar lavage sample obtained at the Chinese PLA General Hospital from 2018–2024 were collected, and pixel-level high-quality instance annotations of seven cell types were labeled. In total, 2,105 clinical images were gathered, with 13,263 cells from seven distinct classes, via both contour fine labeling and bounding box labeling. The dataset was trained and tested by the YOLOv8 instance segmentation network. The results demonstrated that the dataset and model we provided are beneficial for the study of automated cell identification in BALF.