Abstract
IntroductionPrimary antiphospholipid syndrome can be a difficult diagnosis in the absence of typical clinical features. We describe an unusual presentation of primary antiphospholipid syndrome mimicking vasculitis for which the only diagnostic clue on initial presentation was antiphospholipid syndrome nephropathy.Case presentationA 29-year-old Sri Lankan woman presented with features mimicking vasculitis with no obvious clinical features of antiphospholipid syndrome. Classical symptoms of antiphospholipid syndrome only appeared months later. A retrospective analysis showed that the only evidence of antiphospholipid syndrome at her first presentation was antiphospholipid syndrome nephropathy on her renal biopsy.ConclusionsA high degree of suspicion of antiphospholipid syndrome is needed when patients present with non-specific vasculitis features. It has a broad clinical impact as antiphospholipid syndrome can present to any clinician with rare manifestations such as nephropathy. This significantly adds to the advancement of knowledge as antiphospholipid syndrome nephropathy should be recognized as a true entity and considered as a classification criteria for antiphospholipid syndrome.
Highlights
Primary antiphospholipid syndrome can be a difficult diagnosis in the absence of typical clinical features
A high degree of suspicion of antiphospholipid syndrome is needed when patients present with non-specific vasculitis features
It has a broad clinical impact as antiphospholipid syndrome can present to any clinician with rare manifestations such as nephropathy
Summary
This case highlights the importance of having a high degree of suspicion for APS, especially when the presenting features are non-specific. It has a broad clinical impact as APS can present to any clinician with rare manifestations such as nephropathy. This significantly adds to the advancement of knowledge as APSN should be recognized as a true entity and considered as a classification criteria for APS. Consent Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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