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Table 1 Non-criteria manifestations among primary APS patients

From: Non-criteria manifestations in primary antiphospholipid syndrome: a French multicenter retrospective cohort study

Total number = 43

Autoimmune cytopenia

APS nephropathy

Libman-Sachs endocarditis

Neurological non-criteria

Livedo reticularis

Number

17 (39.5)

4 (9.3)

5 (11.6)

12 (27.9)

8 (18.6)

Type, n

ITP = 13

AIHA = 1

Evan’s syndrome = 3

-

-

Multiple sclerosis-like disease = 4

Migraine = 6

Lymphocytic recurrent meningitides = 1

Seizures = 1

-

Associated non-criteria manifestations

APS nephropathy

Livedo reticularis

ITP

Livedo reticularis

Migraine

Livedo reticularis

Libman-Sachs endocarditis

ITP

APS nephropathy

Libman-Sachs endocarditis

Thrombotic phenotype (pure), n (%)

10 (58.8)

2 (50.0)

2 (40.0)

9 (75.0)

4 (50.0)

Obstetrical phenotype (pure), n (%)

3 (17.6)

0 ( 0.0)

0 (0.0)

3 (25.0)

0 (0.0)

Combined APS, n (%)

4 (23.5)

2 ( 50.0)

3 (60.0)

0 (0.0)

4 (50.0)

Triple positivity, n (%)

10 (58.8)

4 (100.0)

3 (60.0)

3 (25.0)

4 (57.1)

Relapse, n/total n (%)

10/12 (83.3)

4/4 (100.0)

1/5 (20.0)

3/10 (30.0)

4/5 (80.0)

  1. AIHA autoimmune hemolytic anemia, APS antiphospholipid syndrome, ITP immune thrombocytopenic purpura