{"title":"世界卫生组织胰胆细胞病理学报告系统。","authors":"Martha B Pitman","doi":"10.5858/arpa.2023-0411-RA","DOIUrl":null,"url":null,"abstract":"<p><strong>Context.—: </strong>The World Health Organization (WHO) Reporting System for Pancreaticobiliary Cytopathology (WHO System) is the product of a joint venture between the World Health Organization, the International Academy of Cytology, and the International Agency for Research on Cancer. The WHO System revises the Papanicolaou Society of Cytopathology System for Reporting Pancreaticobiliary Cytology (PSC System) and replaces the 6-tiered system with a 7-tiered system.</p><p><strong>Objective.—: </strong>To explain the WHO System and the differences with the PSC System.</p><p><strong>Data sources.—: </strong>The WHO System and the PSC System of Reporting Pancreaticobiliary Cytopathology.</p><p><strong>Conclusions.—: </strong>The diagnostic categories of the WHO System are \"Insufficient/Inadequate/Nondiagnostic\"; \"Benign (Negative for Malignancy)\"; \"Atypical\"; \"Pancreaticobiliary Neoplasm, Low Risk/Low Grade (PaN-Low)\"; \"Pancreatic Neoplasm, High Risk/High Grade (PaN-High)\"; \"Suspicious for Malignancy\"; and \"Malignant.\" In the WHO System, the \"benign\" category includes both nonneoplastic and neoplastic lesions, so the \"Neoplastic: Benign\" category of the PSC system has been eliminated. Low-grade malignancies, pancreatic neuroendocrine tumors (PanNETs), and solid-pseudopapillary neoplasm (SPN) classified as \"Neoplastic: Other\" in the PSC System are classified as \"Malignant\" in the WHO System, leaving in the \"Neoplasm\" category intraductal lesions, which are divided into 2 new diagnostic categories: \"Pancreaticobiliary Neoplasm (PaN)-Low Risk/Grade\" and \"PaN-High Risk/Grade.\" As with the PSC System, the WHO System advocates close correlation with imaging and encourages incorporation of ancillary testing into the final diagnosis, such as biochemical (carcinoembryonic antigen [CEA] and amylase) and molecular testing. The WHO System includes risk of malignancy per category, and reporting and diagnostic management options that recognize the variations in resources of low- and middle-income countries.</p>","PeriodicalId":93883,"journal":{"name":"Archives of pathology & laboratory medicine","volume":" ","pages":"e39-e46"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The World Health Organization Reporting System for Pancreaticobiliary Cytopathology: Review and Comparison to the Papanicolaou Society of Cytopathology System.\",\"authors\":\"Martha B Pitman\",\"doi\":\"10.5858/arpa.2023-0411-RA\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Context.—: </strong>The World Health Organization (WHO) Reporting System for Pancreaticobiliary Cytopathology (WHO System) is the product of a joint venture between the World Health Organization, the International Academy of Cytology, and the International Agency for Research on Cancer. The WHO System revises the Papanicolaou Society of Cytopathology System for Reporting Pancreaticobiliary Cytology (PSC System) and replaces the 6-tiered system with a 7-tiered system.</p><p><strong>Objective.—: </strong>To explain the WHO System and the differences with the PSC System.</p><p><strong>Data sources.—: </strong>The WHO System and the PSC System of Reporting Pancreaticobiliary Cytopathology.</p><p><strong>Conclusions.—: </strong>The diagnostic categories of the WHO System are \\\"Insufficient/Inadequate/Nondiagnostic\\\"; \\\"Benign (Negative for Malignancy)\\\"; \\\"Atypical\\\"; \\\"Pancreaticobiliary Neoplasm, Low Risk/Low Grade (PaN-Low)\\\"; \\\"Pancreatic Neoplasm, High Risk/High Grade (PaN-High)\\\"; \\\"Suspicious for Malignancy\\\"; and \\\"Malignant.\\\" In the WHO System, the \\\"benign\\\" category includes both nonneoplastic and neoplastic lesions, so the \\\"Neoplastic: Benign\\\" category of the PSC system has been eliminated. Low-grade malignancies, pancreatic neuroendocrine tumors (PanNETs), and solid-pseudopapillary neoplasm (SPN) classified as \\\"Neoplastic: Other\\\" in the PSC System are classified as \\\"Malignant\\\" in the WHO System, leaving in the \\\"Neoplasm\\\" category intraductal lesions, which are divided into 2 new diagnostic categories: \\\"Pancreaticobiliary Neoplasm (PaN)-Low Risk/Grade\\\" and \\\"PaN-High Risk/Grade.\\\" As with the PSC System, the WHO System advocates close correlation with imaging and encourages incorporation of ancillary testing into the final diagnosis, such as biochemical (carcinoembryonic antigen [CEA] and amylase) and molecular testing. The WHO System includes risk of malignancy per category, and reporting and diagnostic management options that recognize the variations in resources of low- and middle-income countries.</p>\",\"PeriodicalId\":93883,\"journal\":{\"name\":\"Archives of pathology & laboratory medicine\",\"volume\":\" \",\"pages\":\"e39-e46\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of pathology & laboratory medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5858/arpa.2023-0411-RA\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of pathology & laboratory medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5858/arpa.2023-0411-RA","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The World Health Organization Reporting System for Pancreaticobiliary Cytopathology: Review and Comparison to the Papanicolaou Society of Cytopathology System.
Context.—: The World Health Organization (WHO) Reporting System for Pancreaticobiliary Cytopathology (WHO System) is the product of a joint venture between the World Health Organization, the International Academy of Cytology, and the International Agency for Research on Cancer. The WHO System revises the Papanicolaou Society of Cytopathology System for Reporting Pancreaticobiliary Cytology (PSC System) and replaces the 6-tiered system with a 7-tiered system.
Objective.—: To explain the WHO System and the differences with the PSC System.
Data sources.—: The WHO System and the PSC System of Reporting Pancreaticobiliary Cytopathology.
Conclusions.—: The diagnostic categories of the WHO System are "Insufficient/Inadequate/Nondiagnostic"; "Benign (Negative for Malignancy)"; "Atypical"; "Pancreaticobiliary Neoplasm, Low Risk/Low Grade (PaN-Low)"; "Pancreatic Neoplasm, High Risk/High Grade (PaN-High)"; "Suspicious for Malignancy"; and "Malignant." In the WHO System, the "benign" category includes both nonneoplastic and neoplastic lesions, so the "Neoplastic: Benign" category of the PSC system has been eliminated. Low-grade malignancies, pancreatic neuroendocrine tumors (PanNETs), and solid-pseudopapillary neoplasm (SPN) classified as "Neoplastic: Other" in the PSC System are classified as "Malignant" in the WHO System, leaving in the "Neoplasm" category intraductal lesions, which are divided into 2 new diagnostic categories: "Pancreaticobiliary Neoplasm (PaN)-Low Risk/Grade" and "PaN-High Risk/Grade." As with the PSC System, the WHO System advocates close correlation with imaging and encourages incorporation of ancillary testing into the final diagnosis, such as biochemical (carcinoembryonic antigen [CEA] and amylase) and molecular testing. The WHO System includes risk of malignancy per category, and reporting and diagnostic management options that recognize the variations in resources of low- and middle-income countries.