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Article
December 1983

Primary Amyloidosis Presenting as Sjögren's Syndrome

Author Affiliations

From the Department of Medicine, University of New Mexico School of Medicine (Drs Gogel and Volpicelli), and the Research Division, Lovelace Medical Foundation (Dr Searles), Albuquerque; and the Department of Medicine, Dartmouth Medical School, Hanover, NH (Dr Cornwell).

Arch Intern Med. 1983;143(12):2325-2326. doi:10.1001/archinte.1983.00350120123027
Abstract

• A patient had severe sicca complex. Histopathologic and immunologic examination of the salivary glands showed amyloid fibril infiltration, type AλVI. To our knowledge, this is the first documentation of immunologically characterized primary amyloidosis causing the sicca complex. The sicca complex is usually associated with Sjögren's syndrome and the presence of autoantibodies to SSA and SSB. These antibodies were absent in our patient, despite the severity of the sicca syndrome. The clinician should consider more unusual causes of the sicca complex, eg, amyloidosis, particularly if the serologic markers of antibodies to SSA and SSB are absent. Tissue typing the amyloid protein diagnosed primary amyloidosis, obviating the need to search for underlying disease.

(Arch Intern Med 1983;143:2325-2326)

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