[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.205.176.107. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
June 1978

a1-Antitrypsin Deficiency Associated With Persistent Cutaneous VasculitisOccurrence in a Child With Liver Disease

Author Affiliations

From the Departments of Dermatology (Dr Brandrup) and Pediatrics (Dr Østergaard), Odense (Denmark) University Hospital. Dr Brandrup is now with the Department of Dermatology, Gentofte Hospital, Hellerup, Denmark.

Arch Dermatol. 1978;114(6):921-924. doi:10.1001/archderm.1978.01640180055013
Abstract

• α1-Antitrypsin (α1-AT) deficiency is an autosomal recessive inherited disease. The serum concentration of the protease inhibitor (Pi) α1-AT is controlled by a set of codominant allelic genes, constituting the so-called Pi system. Abnormal conditions reported in connection with severe α1-AT deficiency of the PiZZ type have been, in the newborn, cholestasis and progressive juvenile cirrhosis, and in adults, panacinar pulmonary emphysema and liver disease. Skin changes have not been described previously in connection with this disease picture.

The case is persistent cutaneous vasculitis in a 2-year-old child with α1-AT deficiency of the PiZZ type, heterozygosity for the Duarte variant of galactose-1-phosphate uridyl transferase, and neonatal liver disease. A pathogenetic relationship may exist between the biochemical defects and both the skin and liver diseases.

(Arch Dermatol 114:921-924, 1978)

×