Twenty-year follow-up: an unusual case of nephropathy of antiphospholipid syndrome.

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

Lupus

journal_title

Lupus

authors

Lin YQ,Lakshminarayanan S,Yamase H,Palmisano J,Parke A

doi

10.1177/0961203308098629

subject

Has Abstract

pub_date

2009-05-01 00:00:00

pages

564-6

issue

6

eissn

0961-2033

issn

1477-0962

pii

18/6/564

journal_volume

18

pub_type

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