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Observational Study
.2021 Dec;46(8):1530-1541.
doi: 10.1111/ced.14801. Epub 2021 Sep 24.

Line-field confocal optical coherence tomography for actinic keratosis and squamous cell carcinoma: a descriptive study

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Observational Study

Line-field confocal optical coherence tomography for actinic keratosis and squamous cell carcinoma: a descriptive study

E Cinotti et al. Clin Exp Dermatol.2021 Dec.

Abstract

Background: Early and accurate diagnosis of cutaneous squamous cell carcinomas (SCCs) and actinic keratoses (AK) is fundamental to reduce their associated morbidity and to select the correct treatment. Line-field confocal optical coherence tomography (LC-OCT) is a new imaging device that can characterize healthy skin and basal cell carcinoma, but no large studies on keratinocyte cell tumours have yet been published.

Aim: To identify and describe LC-OCT criteria associated with SCC and AK, and to compare LC-OCT findings in these tumours.

Methods: A retrospective observational multicentre study was conducted. Lesions were imaged with the LC-OCT device before surgery and examined histologically. LC-OCT criteria for AK/SCC were identified and their presence was evaluated in all study lesions. Univariate and multivariate analyses were performed to compare AK and SCCs, and to investigate differences between in situ and invasive tumours.

Results: In total, 158 patients with 50 AK and 108 SCCs (62 in situ and 46 invasive) were included. Cytological and architectural alterations were found in most lesions, and differences were found between AK and SCCs. Although the visualization of the dermoepidermal junction (DEJ) was often hampered by hyperkeratosis and acanthosis, an outlined DEJ without broad strands was observed in almost all AK and almost all in situ SCCs, but in only three invasive SCCs (P < 0.001) when the DEJ was detectable.

Conclusion: Our results suggest that LC-OCT can help clinicians in the identification of AK and SCC and their differentiation, providing a real-time and noninvasive examination. Further studies are needed to confirm our data.

© 2021 The Authors. Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

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Figures

Figure 1
Figure 1
(a–d) Actinic keratosis: (a) dermoscopic, (b) histopathological and (c,d) line‐field confocal optical coherence tomography (LC‐OCT) images. (b) Histopathological examination shows mild keratinocyte atypia in the epidermis and prominent hair follicles (white star). (c,d) LC‐OCT examination reveals the presence of atypical keratinocyte nuclei inside the epidermis (red asterisk) and a well‐outlined dermoepidermal junction (DEJ, red arrow). (c) A hair follicle is also present (white star). Scale bar = 100 µm.
Figure 2
Figure 2
(a–c) Actinic keratosis: (a) dermoscopic, (b) histopathological and (c) line‐field confocal optical coherence tomography (LC‐OCT) images. (c) LC‐OCT examination reveals the presence of hyperkeratosis (white brace), acanthosis (yellow brace) and atypical nuclei of keratinocytes inside the epidermis (red asterisk). The dermoepidermal junction is not visible. Roundish hyporeflective areas corresponding to glomerular vessels are discernible (white arrow). Scale bar = 100 µm.
Figure 3
Figure 3
(a–d) Squamous cell carcinomain situ (Bowen subtype): (a) dermoscopic, (b) histopathological and (c,d) line‐field confocal optical coherence tomography (LC‐OCT) images. (c) LC‐OCT examination reveals the presence of hyperkeratosis (white brace), acanthosis (yellow brace), atypical nuclei of keratinocytes inside the epidermis (red asterisk) and roundish hyporeflective areas corresponding to glomerular vessels (white arrow). The dermoepidermal junction is not visible. (d) An erosion with an overlying crust (blue asterisk) is detectable and correlates with (e) histological image. Scale bar = 100 µm.
Figure 4
Figure 4
(a–c) Squamous cell carcinomain situ (Bowen subtype): (a) dermoscopic, (b) histopathological and (c) line‐field confocal optical coherence tomography (LC‐OCT) images. (c) LC‐OCT examination reveals the presence of hyperkeratosis (white brace), acanthosis (yellow brace) and atypical keratinocyte nuclei irregular in size and shape inside the epidermis (red asterisk). The dermoepidermal junction is also visible (red arrow). Roundish hyporeflective areas corresponding to glomerular (white arrow) and linear (light blue) vessels are discernible. Scale bar = 100 µm.
Figure 5
Figure 5
(a–c) Microinvasive squamous cell carcinoma: (a) dermoscopic, (b) histopathological and (c) line‐field confocal optical coherence tomography (LC‐OCT) images. (c) LC‐OCT examination reveals the presence of hyperkeratosis (white brace), acanthosis (yellow brace), atypical nuclei of keratinocyte (red asterisk) and tumour budding (white arrow). Adnexal involvement is present (yellow star). The dermoepidermal junction is well outlined (red arrow), except in focal areas (green asterisk). Scale bar = 100 µm.
Figure 6
Figure 6
(a–c) Invasive squamous cell carcinoma: (a) dermoscopic, (b) histopathological and (c) line‐field confocal optical coherence tomography (LC‐OCT) images. (c) LC‐OCT examination reveals the presence of atypical keratinocyte nuclei irregular in size and shape inside the epidermis (red asterisk). The dermoepidermal junction is not well outlined (green asterisk) and tumour broad strands (yellow asterisk) are visible. Scale bar = 100 µm.
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References

    1. Eigentler TK, Leiter U, Häfner H‐M et al. Survival of patients with cutaneous squamous cell carcinoma: results of a prospective cohort study. J Invest Dermatol 2017; 137: 2309–15. - PubMed
    1. Burton KA, Ashack KA, Khachemoune A. Cutaneous squamous cell carcinoma: a review of high‐risk and metastatic disease. Am J Clin Dermatol 2016; 17: 491–508. - PubMed
    1. Fuchs A, Marmur E. The kinetics of skin cancer: progression of actinic keratosis to squamous cell carcinoma. Dermatol Surg 2007; 33: 1099–101. - PubMed
    1. Fernandez Figueras MT. From actinic keratosis to squamous cell carcinoma: pathophysiology revisited. J Eur Acad Dermatol Venereol 2017; 31(Suppl): 5–7. - PubMed
    1. Neidecker MV, Davis‐Ajami ML, Balkrishnan R, Feldman SR. Pharmacoeconomic considerations in treating actinic keratosis. Pharmacoeconomics 2009; 27: 451–64. - PubMed

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