VASCULITIS AND SJOGRENS SYNDROME WITH IGA-IGG CRYOGLOBULINEMIA TERMINATING IN IMMUNOBLASTIC SARCOMA

被引:41
作者
AIZAWA, Y
ZAWADZKI, ZA
MICOLONGHI, TS
MCDOWELL, JW
NEIMAN, RS
机构
[1] MEMORIAL HOSP, DIV CLIN IMMUNOL & ONCOL, PAWTUCKET, RI 02860 USA
[2] MALLORY INST PATHOL, BOSTON, MA USA
[3] BROWN UNIV, DEPT MED, PROVIDENCE, RI 02912 USA
[4] BROWN UNIV, DEPT PATHOL, PROVIDENCE, RI 02912 USA
[5] BOSTON UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02215 USA
关键词
D O I
10.1016/0002-9343(79)90098-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Generalized lymphadenopathy and other manifestations of Sjögren's syndrome developed in a 68 year old woman with a long history of systemic vasculitis and arthralgia. An unusual immunologic feature was hypogammaglobulinemia and immunoglobulin A (IgA) monoclonal immunoglobulinemia with mixed IgA-IgG cryoglobulin. At autopsy, the histopathologic findings were compatible with immunoblastic sarcoma. The monoclonal IgA protein, found in serum, pleural and pericardial fluids, showed rheumatoid factor activity. Immunocytes from the immunoblastic sarcoma were found to be the source of the monoclonal IgA protein. © 1979.
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页码:160 / 166
页数:7
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