AIMS 2 \& 3: In this study the investigators seek to formally compare reproducibility and accuracy of KS lesion size measurements between SkinScan3D and the current standard of care manual measurement method. The investigators will then test the SS3D device on 100 patients in a variety of real-world practice locations to determine whether the device will be usable, acceptable, appropriate, and feasible in routine care settings.
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Reproducibility of KS lesion size measurements between SkinScan3D and current standard of care measurement - Aim 2 Only
Timeframe: Approximately 3 months
Accuracy of KS lesion size measurements between SkinScan3D and current standard of care measurement - Aim 2 Only
Timeframe: Approximately 3 months
Device usability - Aim 3 Only
Timeframe: 6 months
Acceptability - Aim 3 Only
Timeframe: 6 months
Appropriateness - Aim 3 Only
Timeframe: 6 months
Feasibility - Aim 3 Only
Timeframe: 6 months