2015
DOI: 10.1155/2015/934196
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Takayasu’s Arteritis with Systemic Lupus Erythematosus: A Rare Association

Abstract: We report the case of a 24-year-old nondiabetic, nonhypertensive lady with history of fatigue, dyspnoea and limb claudication. She has been diagnosed with Takayasu's arteritis. Subsequently she developed rash, alopecia, joint pain, and various other laboratory abnormalities which led to a diagnosis of SLE. Takayasu's arteritis (TA) rarely coexists with systemic lupus erythematosus (SLE). The absence of specific SLE markers in patients with TA who subsequently develop SLE suggests that the coexistence of these … Show more

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Cited by 4 publications
(11 citation statements)
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“…In one case report, there was an associated large vessel vasculopathy in a Japanese patient with a background diagnosis of SLE and temporal arteritis [7]. We found a similar case to ours where there was a patient with a Takayasu's arteritis presentation followed by an associated diagnosis of SLE [8]. In this reported case, the patient was a 24 year old Indian female who initially presented with clinical symptoms and signs consistent with a diagnosis of Takayasu's pulseless arteritis.…”
Section: Discussionsupporting
confidence: 77%
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“…In one case report, there was an associated large vessel vasculopathy in a Japanese patient with a background diagnosis of SLE and temporal arteritis [7]. We found a similar case to ours where there was a patient with a Takayasu's arteritis presentation followed by an associated diagnosis of SLE [8]. In this reported case, the patient was a 24 year old Indian female who initially presented with clinical symptoms and signs consistent with a diagnosis of Takayasu's pulseless arteritis.…”
Section: Discussionsupporting
confidence: 77%
“…In this reported case, the patient was a 24 year old Indian female who initially presented with clinical symptoms and signs consistent with a diagnosis of Takayasu's pulseless arteritis. Three years later she then represented with rash, arthralgia, non scarring alopecia and other clinical features of SLE [8]. In our case, the patient similarly presented originally with clinical features more consistent with a diagnosis of Takayasu's pulseless arteritis but with a much more persistently elevated ESR.…”
Section: Discussionsupporting
confidence: 51%
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“…In some cases, medium-sized arteries are involved, which are associated with more frequent thrombotic events and higher morbidity. 11,12 In SLE, involvement of aorta is extremely rare. 13 In our case who was a diagnosed case of SLE, we found the typical angiographic evidence of Takayasu's arteritis effecting the great vessels.…”
Section: Discussionmentioning
confidence: 99%
“…The age of onset and sex predominance (female) were similar in both conditions. Additionally, the antiphospholipid syndrome observed in SLE may mimic the vascular-occlusive symptoms observed in TA (10). Notably, approximately 56% of individuals with SLE experience vasculitis at some point in their lives (11).…”
Section: Introductionmentioning
confidence: 99%