2006
DOI: 10.1007/s10067-006-0277-3
|View full text |Cite
|
Sign up to set email alerts
|

Rare association of antiphospholipid syndrome and Takayasu arteritis

Abstract: The antiphospholipid syndrome (APS) is characterized by obstetric and thrombotic complications in the presence of antiphospholipid antibodies. It can happen in an isolated way or in association with diffuse connective tissue diseases, mainly systemic lupus erythematosus. The association of APS with Takayasu arteritis (TA) is rarely described in the literature. We described a case of primary APS in a female patient who developed obstruction in large-size arteries, in spite of the use of oral anticoagulant, and … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
10
0

Year Published

2007
2007
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(10 citation statements)
references
References 6 publications
0
10
0
Order By: Relevance
“…The nonspecific symptoms of this patient could have been the manifestation of this vasculitis (10,11). Furthermore, Takayasu arteritis has been described to be associated with aPL, with and without clinical thrombosis (12)(13)(14)(15). In our patient, however, physical examination failed to reveal any cardinal signs of Takayasu arteritis such as claudication, vascular bruits, or varying BP between extremities.…”
Section: Vasculitismentioning
confidence: 51%
“…The nonspecific symptoms of this patient could have been the manifestation of this vasculitis (10,11). Furthermore, Takayasu arteritis has been described to be associated with aPL, with and without clinical thrombosis (12)(13)(14)(15). In our patient, however, physical examination failed to reveal any cardinal signs of Takayasu arteritis such as claudication, vascular bruits, or varying BP between extremities.…”
Section: Vasculitismentioning
confidence: 51%
“…93 There is debate in the literature as to the significance of aortic occlusive disease in primary APS 94,95 ; whether this lesion is thrombotic or inflammatory is not readily distinguishable with conventional imaging, and tissue is rarely accessible. 96 However, in most case reports patients were successfully treated with corticosteroids, suggesting an inflammatory etiology.…”
Section: Takayasu Arteritismentioning
confidence: 99%
“…Thereafter, case reports suggesting the usefulness of infliximab for the treatment of refractory Takayasu disease have appeared from various countries including Japan. [15][16][17][18][19] Evaluation by large-scale comparative controlled studies is necessary in the future.…”
Section: Usefulness Of Infliximab For the Treatment Of Anca-associatementioning
confidence: 99%