Remote cutaneous confocal microscopy: A multicentric prospective study evaluating diagnostic accuracy for melanoma and keratinocyte carcinoma in tertiary settings

Cutaneous confocal microscopy (CCM) facilitates in vivo visualization of skin at a cellular level. Use of a “store and forward” approach for remote-CCM interpretation (remote-CCM) across multiple sites has not been tested and may increase access to noninvasive diagnosis. To test the diagnostic accur...

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Veröffentlicht in:Journal of the American Academy of Dermatology 2024-10
Hauptverfasser: Ho, Genevieve, Collgros, Helena, Sinz, Christoph, Melhoranse-Gouveia, Bruna, Gallo, Bruna, Chew, Christopher Y., Ip, Ken, Koutsis, James, Lo, Serigne N., Schwartz-Aldea, Rodrigo, Herbert Chan, Hsien, Ferguson, Peter, Gribbin, Hannah, Mar, Victoria, Soyer, Hans Peter, Martin, Linda K., Smith, Andrea L., Cust, Anne E., Guitera, Pascale
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Sprache:eng
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Zusammenfassung:Cutaneous confocal microscopy (CCM) facilitates in vivo visualization of skin at a cellular level. Use of a “store and forward” approach for remote-CCM interpretation (remote-CCM) across multiple sites has not been tested and may increase access to noninvasive diagnosis. To test the diagnostic accuracy and safety of remote-CCM. We prospectively recruited lesions selected for biopsy for skin malignancy across 5 Australian tertiary dermatology centers. CCM, clinical and dermatoscopy images were acquired prebiopsy and accessed by a cloud-based platform for interpretation by CCM readers. CCM diagnosis was compared with histopathology results. Among the 201 lesions included, melanoma was the most common malignancy (34/72, 47.2%). Of the 89 lesions (44.8%) potentially “saved” from biopsy, 80 (90%) were truly benign lesions and 9 (10.1%) were missed malignant lesions of melanoma in situ (n = 7) and squamous cell carcinoma (SCC) (n = 2). No invasive melanomas were missed. Sensitivity of remote-CCM for detection of malignancy was 89% (95% CI, 79%-95%) and specificity was 64% (95% CI, 55%-73%). The study recruited from high-risk populations and excluded lesions that were not biopsied. Remote-CCM has comparable accuracy to bedside CCM and safely reduces unnecessary biopsies. Potential SCCs are not appropriate for remote-CCM. Follow-up of borderline melanocytic lesions is recommended.
ISSN:0190-9622
1097-6787
1097-6787
DOI:10.1016/j.jaad.2024.09.051