J. Son1, E. Lawson1, S. Selvaggi2, B. Harms1, E. Carchman1, R. Striker3, C. I. Voils1, C. B. Geltzeiler1, C. B. Geltzeiler1 1University Of Wisconsin,Colorectal Surgery,Madison, WI, USA 2University Of Wisconsin,Pathology,Madison, WI, USA 3University Of Wisconsin,Infectious Disease,Madison, WI, USA
Introduction:
Anal dysplasia screening and surveillance guidelines are poorly defined and based on little data. Although recommendations on type of surveillance are controversial, most practitioners recommend follow-up clinical examination for patients with an abnormal anal pap smear. Our objective was to determine how often an anal pap was followed by clinical exam at our institution and how often histology correlated with pap cytology.
Methods:
All anal pap results at a single tertiary academic center from 2008 to 2018 were collected. Retrospective chart review was performed on all patients with cytology results demonstrating dysplasia (high-grade squamous intraepithelial lesions (HSIL) or low-grade squamous intraepithelial lesions (LSIL)). We examined patient risk factors as well as their clinical follow-up within 1 year. Clinical exam was defined as digital rectal examination, anoscopy, or high resolution anoscopy (HRA). We also examined if cytology accurately predicted histologic dysplasia.
Results:
A total of 327 anal pap smears demonstrated dysplasia (25% HSIL and 75% LSIL) in 182 patients. 92% of patients were male, 97% HIV positive, and 73% had documented anal receptive intercourse. 75% of dysplastic anal paps were followed by clinical exam within 1 year and 50% were biopsied. Of the 45 HSIL anal paps that were followed by biopsy, only 38% confirmed high-grade disease on histology, 24% demonstrated low-grade disease, and the remaining were negative. In contrast, of the 119 LSIL anal paps that were followed by biopsy, 44% confirmed low-grade disease on histology, 22% were upgraded to high-grade disease. 3% had invasive squamous cell carcinoma on biopsy after LSIL pap.
Conclusion:
This single center study demonstrates that only 75% of abnormal anal paps were followed up with clinical exam within 1 year and only 50% were biopsied for histologic confirmation. When biopsied, only 66% of dysplastic paps demonstrated dysplasia or invasive disease on histologic examination. There is room for improvement in our institution to consistently follow-up with clinical exam after abnormal pap. Our data suggests this is especially important considering anal pap cytology is an imperfect predictor of histologic dysplasia and invasive disease. Clinical exam may be more important as the initial screening test.