Literature DB >> 3034714

Diffuse hepatocellular dysplasia and carcinoma associated with the Mmalton variant of alpha 1-antitrypsin.

C L Reid, G J Wiener, D W Cox, J E Richter, K R Geisinger.   

Abstract

The cirrhosis and hepatocellular carcinoma associated with alpha 1-antitrypsin deficiency has been exclusively reported with the PI Z allele. We present a 63-yr-old white man with emphysema, cirrhosis, and hepatocellular carcinoma. The latter occurred on a background of diffusely distributed hepatocellular dysplasia. Serum protein electrophoresis suggested a deficiency of alpha 1-antitrypsin quantitated at 13% of normal. PI phenotyping showed that he had only the rare PI Mmalton allele, previously associated only with severe lung disease. Family studies demonstrated the distribution of this rare allele. The liver at autopsy displayed well-differentiated hepatocellular carcinoma in addition to alpha 1-antitrypsin deposits in normal, dysplastic, and malignant cells.

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Year:  1987        PMID: 3034714     DOI: 10.1016/0016-5085(87)90332-5

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  4 in total

1.  In-frame single codon deletion in the Mmalton deficiency allele of alpha 1-antitrypsin.

Authors:  G C Fraizer; T R Harrold; M H Hofker; D W Cox
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025

Review 2.  Diagnosis and management of patients with α1-antitrypsin (A1AT) deficiency.

Authors:  David R Nelson; Jeffrey Teckman; Adrian M Di Bisceglie; David A Brenner
Journal:  Clin Gastroenterol Hepatol       Date:  2011-12-23       Impact factor: 11.382

3.  A null deficiency allele of alpha 1-antitrypsin, QOludwigshafen, with altered tertiary structure.

Authors:  G C Frazier; M A Siewertsen; M H Hofker; M G Brubacher; D W Cox
Journal:  J Clin Invest       Date:  1990-12       Impact factor: 14.808

4.  Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous, compound heterozygous and heterozygous states.

Authors:  Philippe Joly; Olivier Guillaud; Valérie Hervieu; Alain Francina; Jean-François Mornex; Colette Chapuis-Cellier
Journal:  Orphanet J Rare Dis       Date:  2015-10-07       Impact factor: 4.123

  4 in total

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