Concurrent systemic AA amyloidosis can discriminate primary sclerosing cholangitis from IgG4-associated cholangitis

doi:10.3748/wjg.v18.i2.192

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Jan 14, 2012 (publication date) through Nov 24, 2024

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World Journal of Gastroenterology

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1007-9327

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

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World J Gastroenterol. Jan 14, 2012; 18(2): 192-196
Published online Jan 14, 2012. doi: 10.3748/wjg.v18.i2.192

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Figure 2 Histology of the salivary glands and the sto-mach by hematoxylin and eosin stain (200 ×). Amorphous eosinophilic materials in the subglandular and stroma of the salivary glands (A) and submucosal stroma of the stomach (B) were demonstrated. They were found to be Congo-red-positive. Immunohistochemical staining with anti-human amyloid A antibody (200 ×) confirmed a positive AA stain in the salivary glands (C) and stomach (D).

Citation: Kato T, Komori A, Bae SK, Migita K, Ito M, Motoyoshi Y, Abiru S, Ishibashi H. Concurrent systemic AA amyloidosis can discriminate primary sclerosing cholangitis from IgG4-associated cholangitis. World J Gastroenterol 2012; 18(2): 192-196
URL: https://www.wjgnet.com/1007-9327/full/v18/i2/192.htm
DOI: https://dx.doi.org/10.3748/wjg.v18.i2.192