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A Closer Look at Dowling-Degos Disease: A Case Report and Quantitative Assessment of Its Surface Texture Parameters
Catherine F Sollitto1, Claire Wolinsky2, Brian L Beatty3
1College of Osteopathic Medicine, New York Institute of Technology, Old Westbury, USA.
Abstract:
Dowling-Degos disease (DDD) is a rare genodermatosis characterized by reticulated hyperpigmented macules and papules, yet its surface architecture has not been quantitatively described. In this case, we utilized 3D surface metrology to objectively characterize its surface texture. A shave biopsy from the inner thigh of a 54-year-old woman with clinically and histopathologically confirmed DDD was scanned using the S Neox optical profiler (Sensofar, Barcelona, Spain) at 20x and 50x magnification. Roughness parameters, including mean roughness (Sa), maximum surface height (Sz), maximum valley depth (Sv), maximum peak height (Sp), root mean square roughness (Sq), skewness (Ssk), and sharpness (Sku), were extracted and compared with previously published values for both unaffected and psoriatic skin. When compared to unaffected skin, DDD showed markedly increased Sa, Sz, and Sv, indicating a more irregular and deeply sculpted skin surface. In contrast to psoriatic lesions, DDD demonstrated lower Sa. Between magnifications, Sp was significantly greater in the 20x scan. These findings indicate that DDD has a distinct topographic profile that could support noninvasive diagnosis and monitoring. Surface metrology may complement clinical, dermoscopic, and histopathologic evaluation by providing a quantitative description of disease-specific skin texture.

