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Sorted By Test Name - Mayo Medical Laboratories

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82039<br />

89118<br />

cervical cytological abnormalities. JAMA 2002;287:2120-2129<br />

ThinPrep Diagnostic Without Physician Interpretation<br />

Clinical Information: The ThinPrep PAP <strong>Test</strong> (TPPT) is an alternative preparation method for the<br />

cervical pap screening test. The method utilizes a liquid-base technique that replaces the direct smear<br />

method of the conventional PAP screen. This method is one of several new technologies developed to<br />

improve visualization of cellular material by reducing smearing trauma, air drying artifact, and obscuring<br />

blood and inflammation. In addition, variability in smearing technique is eliminated as the majority of<br />

processing and preparation is performed in the laboratory under controlled conditions.<br />

Useful For: Routine cytology screen for cervical abnormalities. The method is an alternative to<br />

conventional PAP smears.<br />

Interpretation: Standard reporting, as defined by the Bethesda System (TBS) is utilized.<br />

Reference Values:<br />

Satisfactory for evaluation. Negative for intraepithelial lesion or malignancy.<br />

Note: Abnormal results will be reviewed by a pathologist at an additional charge.<br />

Clinical References: 1. Austin RM, Ramzey I: Increased detection of epithelial cell abnormalities by<br />

liquid-based gynecologic cytology preparations. A review of accumulated data. Acta Cytol<br />

1998;42:178-184 2. Guidos BJ, Selvaggi SM: Use of the ThinPrep PAP test in clinical practice. Diagn<br />

Cytopathol 1999;20:70-73 3. Kurman RJ, Solomon D: The Bethesda system for reporting cervical/vaginal<br />

cytologic diagnoses: definitions, criteria, and explanatory notes for terminology and specimen adequacy.<br />

New York, NY, Springer-Verlag, 1994 4. Gay JD, Donaldson LD, Goellner JR: False-negative results in<br />

cervical cytologic studies. Acta Cytol 1985;29:1043-1046<br />

ThinPrep Screen with HPV for Women 30 Years and Older<br />

Clinical Information: The majority (>99%) of cervical epithelial neoplasms are the result of human<br />

papillomavirus (HPV) infection. "High-risk'' HPV types (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and<br />

68) can result in both low-grade squamous intraepithelial lesions (LSIL) and high-grade squamous<br />

intraepithelial lesions (HSIL), as well as invasive carcinomas.(1,2) Patients with both a negative cytology<br />

and negative HPV have been shown to be at extremely low risk for cervical neoplasia.(1,2) For women 30<br />

years old and older who have received a negative Pap test and concurrent negative HPV result, the<br />

American Cancer Society (ACS) and American College of Obstetricians and Gynecologists (ACOG)<br />

recommendations for cervical screening state that physicians may lengthen the screening interval to 3<br />

years when using the combined test. Patients deemed to be high-risk by the clinician should still be<br />

screened more frequently. The presence of high risk HPV types in cervical specimens identifies a<br />

subgroup of patients with a greater likelihood of having a high grade squamous intraepithelial lesion.<br />

Current guidelines for follow up of a cytology-negative/HPV-positive patient recommend repeat HPV<br />

testing in 12 months.(2)<br />

Useful For: Detection of cervical carcinoma or intraepithelial lesions and the presence or absence of<br />

high-risk HPV when screening women over the age of 30 for possible cervical neoplasia<br />

Interpretation: The cytology report issued on gynecologic specimens is an estimate of the nature of<br />

the abnormality using the Bethesda nomenclature.(3) Specimen adequacy is characterized as:<br />

-Satisfactory for evaluation (with quality indicators, if applicable) -Unsatisfactory for evaluation, further<br />

subdivided as follows: --Specimen processed and examined but unsatisfactory for evaluation of epithelial<br />

abnormality because of inadequate cellularity, obscuring blood or inflammation, etc. --Specimen rejected<br />

because of a broken slide, unlabeled specimen, etc. The diagnostic interpretation may include: -Negative<br />

for intraepithelial lesion or malignancy (NIL) -Atypical squamous cells of undetermined significance<br />

(ASCUS) characterized as either: --atypical squamous cells of undetermined significance --atypical<br />

squamous cells, cannot exclude HSIL -Low-grade squamous intraepithelial lesion (LSIL), which includes<br />

mild squamous dysplasia (cervical intraepithelial neoplasia I [CINI]) and koilocytotic changes consistent<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1729

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