| Literature DB >> 33585096 |
Gilles J Hoilat1, Ayesha Khan2, Umair Masood3, Anuj Sharma3, Divey Manocha3.
Abstract
Alpha-1 antitrypsin deficiency has been known to cause pulmonary and hepatic diseases. Cirrhosis in patients with alpha-1 antitrypsin deficiency, especially in a homozygotes ZZ phenotype, has been described to occur exclusively as a congenital disease. We present the case of a young 28-year-old female who was initially followed for thrombocytopenia and was found to have cirrhosis of the liver with autoimmune histological features suggesting the possibility that another "second hit" can contribute to a more rapid progression of liver disease.Entities:
Keywords: alpha-1 antitrypsin; autoimmune cirrhosis; live cirrhosis; liver biopsy
Year: 2021 PMID: 33585096 PMCID: PMC7872947 DOI: 10.7759/cureus.12606
Source DB: PubMed Journal: Cureus ISSN: 2168-8184