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Jonathan L. Held, MD; David N. Silvers, MD; Marc E. Grossman, MD
Department of Dermatology and Dermatopathology Columbia University Medical Center 630 W 168 St New York, NY 10032

Arch Dermatol. 1989;125(2):297-299.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

To the Editor.—

Porphyria cutanea tarda (PCT) is often associated with melasmalike hyperpigmentation, as well as hyperpigmentation of the neck, upper chest, and hands.^1-8 Rarely, diffuse melanosis mimicking Addison's disease occurs.^3,5,9 We describe two patients with PCT and acquired hyperpigmentation of the lower extremities. To our knowledge, this association has not been previously described.

Report of Cases.—CASE 1.—

A 47-year-old woman had skin fragility and bullae on her hands. Diagnosis of PCT was confirmed by a 24-hour urinary uroporphyrin level of 1840 µg and thin-layer chromatographic demonstration of fecal isocoproporphyrin. The patient received several phlebotomies, her skin symptoms abated, and two years later the 24-hour urinary uroporphyrin level had decreased to 202 µg.

After a three-year hiatus, the patient returned because of hand blistering, sclerodermoid changes of the skin of her chest, and onset of lower extremity hyperpigmentation (Fig 1). Her 24-hour urinary uroporphyrin level was . . . [Full Text PDF of this Article]

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