Agranulocytosis in Sjogren's syndrome: Two case reports and analysis of 11 additional reported cases

Objectives: To report 2 patients who presented with agranulocytosis that was found to be immune-mediated and associated with occult primary Sjogren's syndrome (1degreesSS) and to identify and study similar cases reported in the literature. Methods: Two patients encountered in 2 large medical centers over a period of 5 years were studied in detail. All reported cases of agranulocytosis in 1degreesSS identified through a MEDLINE search were reviewed. Results: Two patients presented with marked systemic symptoms alone or associated with recurrent infections. Agranulocytosis with either a pattern of maturation arrest or a hypercellular reactive bone marrow was found and was associated with "acute phase" markers, hypergammaglobulinemia, a small paraprotein peak, and high rheumatoid factor titers. A diagnosis of immune-mediated agranulocytosis associated with an occult 1degreesSS was established and was successfully treated with intravenous immunoglobulins or prednisone. Both patients subsequently developed skin vasculitis. This rare association of agranulocytosis and Sjogren's syndrome was identified in 11 other cases and was the presenting manifestation of 1degreesSS in 10 of 13 (77%) patients. Conclusions: Agranulocytosis should be recognized as a rare but well-established association of 1degreesSS. Bone marrow neutrophil production may be affected, or neutrophils may be destroyed in the circulation, by both humoral and cellular immune-mediated mechanisms. Agranulocytosis or neutropenia should be added to the varied hematologic manifestations of 1degreesSS and may be its presenting feature and an important clue to diagnosis.