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Pathology and pathobiology
of actinic (solar) keratosis - an update.Br
J Dermatol. 2007 Dec;157 Suppl 2:18-20.
Actinic keratosis is
a UV light-induced lesion and develops mostly in fair-skinned patients being
susceptible to solar damage. The term actinic keratosis (AK) describes
clinically ill-defined reddish to reddish-brown scaly lesions on
erythematous base in areas damaged severely by sunlight. The term does not
imply anything about the biology or histopathology. Actinic keratoses (AKs)
have been recognized as precursor of cancer or of precancerous lesions in
the past but today they are considered as an early in situ squamous cell
carcinoma (1,2) and are categorized in several classifications with
subdivisions into three grades depending on the amount of atypical
keratinocytes in the epidermis.(3-6) The incidence of development of AK in
caucasians increases with age, proximity to the equator and outdoor
occupation. Australia has the highest skin cancer rate in the world. AKs are
discovered in up to 40-50% of the Australian population older than 40
years.(7) AKs are the most common malignant lesion of the skin.(8-12).
Cytological diagnosis of
basal cell carcinoma and actinic keratosis, using Papanicolaou and May-Grünwald-Giemsa
stained cutaneous tissue smear.Cytopathology.
2007 Oct 4.
Objective: Cytology
may become the diagnostic method of choice with the advent of new
non-invasive treatments for non-melanoma skin cancer, as the sampling
technique for cytology entails little tissue disfiguration. The aim of this
study was to compare and evaluate the diagnostic performance of scrape
cytology using two different cytological staining techniques, and to
evaluate additional touch imprint cytology, with that of histopathology of
basal cell carcinoma (BCC) and actinic keratosis (AK). Methods: We
investigated 50 BCC and 28 AK histologically verified lesions, from 41 and
25 patients, respectively. Two separate skin scrape samples and one touch
imprint sample were taken from each lesion. The smears were stained with
Papanicolaou (Pap) or May-Grünwald-Giemsa (MGG) stains. All cytological
specimens were examined in random order by pathologists without knowledge of
the histology. Cytodiagnostic results were compared with the
histopathological report. Results: Scrape cytodiagnosis agreed with
histopathology in 48 (Pap) and 47 (MGG) of the 50 BCC cases, and in 26 of 28
(Pap) and 21 of 26 (MGG) AK cases, yielding sensitivities of 96%, 94%, 93%
and 81%, respectively. No significant difference in sensitivity between the
two staining methods was found but a trend towards higher Pap sensitivity
for AK was noted (P = 0.10). Touch imprint cytology confirmed histopathology
in 38 of the 77 cases of BCC and AK. Conclusion: Cytological diagnosis with
either Pap or MGG stain for BCC and AK is reliable, and differentiates well
between BCC and AK. Imprint cytology proved to be non-diagnostic in half of
the examined cases.
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