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The International System for Reporting Serous Fluid Cytopathology-An Updated Review
Minhua Wang1, Ashish Chandra2, Guoping Cai1
1Department of Pathology, Yale School of Medicine, New Haven, CT, USA.
Summary
The International System (TIS) for reporting serous fluid cytopathology standardizes diagnoses. This review summarizes TIS, aiding pathologists and clinicians in interpreting serous fluid specimens for improved accuracy.
Area of Science:
- Cytopathology
- Oncology
- Medical Diagnostics
Background:
- Standardized reporting in serous fluid cytopathology is crucial for accurate diagnoses.
- The International System (TIS) for reporting serous fluid cytopathology was established in December 2020.
- Existing reporting lacked standardization, impacting diagnostic reproducibility and communication.
Purpose of the Study:
- To provide an updated summary of the International System (TIS) for reporting serous fluid cytopathology.
- To discuss the TIS five-tier system: nondiagnostic, negative for malignancy, atypia of uncertain significance, suspicious for malignancy, and malignant.
- To review risk of malignancy, diagnostic pitfalls, and a practical approach for serous fluid specimens.
Main Methods:
- Review of the published International System (TIS) for serous fluid cytopathology.
- Analysis of the TIS five-tier diagnostic categories.
- Synthesis of information on risk of malignancy and diagnostic challenges.
Main Results:
- The TIS provides a standardized five-tier system for serous fluid cytopathology reporting.
- Implementation of TIS aims to enhance diagnostic reproducibility and inter-observer agreement.
- The system categorizes specimens from nondiagnostic to malignant, guiding clinical management.
Conclusions:
- The International System (TIS) offers a standardized framework for serous fluid cytopathology.
- Understanding TIS is essential for accurate interpretation and improved patient care.
- This review highlights key aspects of TIS, including its application and potential challenges.

