To the Editor.—
We describe a patient with a combination of acral and flexural hyperpigmentary features characteristic of both Kitamura acropigmentatio reticularis (KAR) and Dowling-Degos disease (DDD). The findings demonstrated in this patient support the concept that KAR and DDD are variable expressions of one genetic disorder.
Report of a Case.—
A 36-year-old Hispanic woman had asymptomatic acral pigmentation that had gradually progressed for 30 years. Sharply demarcated 1- to 5-mm depressed pigmented macules in a reticulate pattern were noted on the dorsal and lateral aspects of her hands, wrists, ankles, and feet. She had noted a similar, bilateral, progressive, axillary, macular hyperpigmentation for approximately 10 years (Fig 1). Her palms revealed pits and linear breaks disrupting the epidermal ridge pattern (Fig 2).Skin biopsy specimens from both the depressed pigmented skin and adjacent normal-appearing skin were obtained from the dorsal web spaces of the hand. A biopsy specimen of
Tappero JW, Kershenovich J, Berger TG. Combined Acral and Flexural Reticulate Pigmentary Anomaly. Arch Dermatol. 1992;128(10):1411–1412. doi:10.1001/archderm.1992.01680200123032
Customize your JAMA Network experience by selecting one or more topics from the list below.
Create a personal account or sign in to: