The effect of cautery artifact on the ability to accurately diagnose dyspla
sia and predict abnormal follow-up in large loop excision specimens of the
transformation zone (LLETZ) has not been adequately addressed in the pathol
ogy literature. One hundred consecutive conization specimens with cytologic
and/or histologic follow-up were studied. Indications for the procedure we
re high-grade squamous intraepithelial lesion (on Pap smear and/or biopsy)
in 64 cases, low-grade squamous intraepithelial lesion in 28? atypical squa
mous cells of unknown significance (ASCUS) in 3, atypical glandular cells o
f unknown significance in 2, adenocarcinoma in situ, squamous carcinoma in
situ, and invasive squamous carcinoma in 1 each. Twenty-four specimens were
cold-knife conizations (CKCs) and 76 LLETZs. All LLETZs had at least 1+ ar
tifact, and in 46 cases (61%) it interfered with at least one aspect of eva
luation. In 21 cases (28%), 1+ artifact interfered only with margin assessm
ent. In 25 cases (33%), there was 2+ or 3+ artifact precluding not only mar
gin assessment, but also diagnosis and grading of dysplasia. Of the 43 LLET
Zs received in more than one piece, 33 (77%) had interfering artifact, and
in 21 (49%) it was 2+ or 3+, at least focally interfering with diagnosis an
d grading. In contrast, of 33 LLETZs received in a single piece, only 13 (3
9%) had interfering artifact, which was 2+ or 3+ in 4 (12%), (p < 0.05). Po
sitive follow-up (including ASCUS, favor dysplasia, and ASCUS, not otherwis
e specified) was found in 6 of 7 CKCs with positive margins (86%), 10 of 16
LLETZs with positive margins (63%), and 4 of 7 LLETZs with unassessable ma
rgins (57%). In cases with negative cone margins, positive follow-up was fo
und in 2 of 17 CKCs (12%), and 18 of 53 LLETZs (34%), p < 0.05; a higher fr
equency of interfering artifact (p<0.05) was seen in these cases. LLETZ mar
gin status and postprocedure endocervical curettage (ECC) specimens were no
t good predictors of residual disease, unlike margin status in CKC. Post-CK
C ECC was a better predictor of subsequent abnormal follow-up than post-LLE
TZ ECC (p < 0.05). The presence of interfering artifact was only rarely men
tioned in the original pathology report. In conclusion, the status of margi
ns is a better predictor of abnormal follow-up in CKC than in LLETZ specime
ns. Fragmentation of the specimen is an additional factor, compounding the
inevitable artifact. Postprocedure ECC is not a useful indicator of residua
l dysplasia. The pathologist should not hesitate to comment on specimen ade
quacy in surgical pathology reports.