| Literature DB >> 35908966 |
Atsuhiko Suenaga1,2, Naoki Sawa1, Yoichi Oshima3, Daisuke Ikuma1, Yuki Oba1, Masayuki Yamanouchi1, Eiko Hasegawa3, Hiroki Mizuno1, Akinari Sekine1, Tatsuya Suwabe1, Kei Kono4, Keiichi Kinowaki4, Kenichi Ohashi4,5, Tamiko Takemura6, Yutaka Yamaguchi7, Motoaki Miyazono2, Tatsuya Atsumi8, Yoshifumi Ubara1.
Abstract
A 42-year-old Japanese woman was admitted for the evaluation of proteinuria. She had a history of four habitual abortions and valvular heart disease, including severe mitral regurgitation and moderate tricuspid regurgitation. A kidney biopsy showed fibrointimal thickening of interlobular arteries, fibrin thrombosis, and associated focal segmental sclerosis. Although the standard test for antiphospholipid (aPL) antibodies was negative, the patient was diagnosed with antiphospholipid syndrome (APS)-related disease by testing for phosphatidylserine dependent anti-prothrombin anticardiolipin antibody, a non-criterial aPL antibody. A kidney biopsy may lead to a diagnosis of APS in patients with negative laboratory test findings for APS.Entities:
Keywords: antiphospholipid antibody syndrome nephropathy; antiphospholipid syndrome; systemic lupus erythematosus
Year: 2022 PMID: 35908966 DOI: 10.2169/internalmedicine.0302-22
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.282