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The adequacy of Pap test collection is
determined by:
1. Accurate patient and specimen identification.
2. Pertinent clinical history.
3. The presence of an adequate squamous component.
4. The presence of an adequate endocervical component (in premenopausal
females with a cervix).
5. The absence of obscuring entities, including inflammation,
blood and contaminants such as talc or lubricant.
6. Adequate cellular preservation.
The adequacy of Non-gynecological specimen
collection is determined by:
1. Accurate patient and specimen identification.
2. Pertinent clinical history.
3. The presence of adequate site-specific cellular material and/or
diagnostic cellular material.
4. Adequate cellular preservation.
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