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Large Intracranial Arteritis with Giant Cells in Systemic Lupus Erythematosus

DOUGLAS SCHARRE, M.D.; MICHELLE PETRI, M.D.; ELAINE ENGMAN, M.D.; and STEPHEN DeARMOND, M.D., Ph.D.
[+] Article and Author Information

▸Requests for reprints should be addressed to Michelle Petri, M.D.; U-426, University of California Medical Center, Third and Parnassus Avenues; San Francisco, CA 94143.


University of California, San Francisco, and Letterman Army Medical Center; San Francisco, California


© 1986 American College of PhysiciansAmerican College of Physicians


Ann Intern Med. 1986;104(5):661-662. doi:10.7326/0003-4819-104-5-661
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This excerpt has been provided in the absence of an abstract.

Neuropsychiatric manifestations in systemic lupus erythematosus have been reported extensively, but the central nervous system pathology has rarely been documented (1, 2). We studied the case of a patient who died with arteritis and occlusion of the left middle and posterior cerebral arteries. An arteritis with giant cells has not been described previously in systemic lupus erythematosus.

A 29-year-old woman had had systemic lupus erythematosus for 3 years with Raynaud's phenomenon; mouth ulcers; polyarthritis; serositis; and diffuse proliferative glomerulonephritis. Tests for antinuclear antibody, anti-double-stranded DNA, and Sm antigen were positive. Recurrent flares were associated with headaches. Diffuse proliferative glomerulonephritis with

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