Primary biliary cirrhosis and hereditary hemorrhagic telangiectasia: When two rare diseases coexist

doi:10.4254/wjh.v5.i5.288

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May 27, 2013 (publication date) through Aug 25, 2024

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World Journal of Hepatology

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1948-5182

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Hepatol. May 27, 2013; 5(5): 288-291
Published online May 27, 2013. doi: 10.4254/wjh.v5.i5.288

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Figure 1 Focal nodular hyperplasia. A: Fibrous septa (green) giving a nodular appearance to liver parenchyma. Masson’s trichrome staining; original magnification × 40; B: Diffuse CD34 positive immunostaining in the sinusoids; original magnification × 100.

Citation: Macaluso FS, Maida M, Alessi N, Cabibbo G, Cabibi D. Primary biliary cirrhosis and hereditary hemorrhagic telangiectasia: When two rare diseases coexist. World J Hepatol 2013; 5(5): 288-291
URL: https://www.wjgnet.com/1948-5182/full/v5/i5/288.htm
DOI: https://dx.doi.org/10.4254/wjh.v5.i5.288