Abstract:
:Nephropathy of antiphospholipid antibody syndrome (NAPS) is an increasingly well-recognized aspect of antiphospholipid syndrome. The most characteristic histopathology is that of thrombotic microangiopathy, and thrombosis occurring in the renal vasculature is thought to be the initiating event. Other less common pathologies have been reported, and the mechanisms of these are unclear. Therapy has been largely empiric. We report a case of NAPS in a patient with atypical pathology, who has declined therapy with immunosuppressive agents and anticoagulants and who has maintained normal renal function in 20 years of follow-up.
journal_name
Lupusjournal_title
Lupusauthors
Lin YQ,Lakshminarayanan S,Yamase H,Palmisano J,Parke Adoi
10.1177/0961203308098629subject
Has Abstractpub_date
2009-05-01 00:00:00pages
564-6issue
6eissn
0961-2033issn
1477-0962pii
18/6/564journal_volume
18pub_type
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