Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias.

Abstract:

:Porphyria cutanea tarda is a photocutaneous syndrome characterized clinically by cutaneous fragility, bullae, hypertrichosis, pigmentary changes, and sclerodermoid plaques and characterized biochemically by hepatic overproduction and storage of excessive amounts of porphyrins. Porphyria cutanea tarda, the most common disorder of porphyrin metabolism, must be differentiated from variegate porphyria, hereditary coproporphyria, bullous dermatosis of hemodialysis, and drug-related pseudoporphyria.

journal_name

Dermatol Clin

journal_title

Dermatologic clinics

authors

Grossman ME,Poh-Fitzpatrick MB

subject

Has Abstract

pub_date

1986-04-01 00:00:00

pages

297-309

issue

2

eissn

0733-8635

issn

1558-0520

journal_volume

4

pub_type

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