Autor: |
Bandyopadhyay D; Department of Accident and Emergency, Lady Hardinge Medical College, New Delhi, India., Ganesan V; Department of Internal Medicine, KB Hostel, RG Kar Medical College, Room No. 38, Khudiram Bose Sarani, Kolkata, West Bengal 700004, India., Bhar D; Department of Internal Medicine, RG Kar Medical College, Kolkata, India., Bhowmick D; Department of Internal Medicine, RG Kar Medical College, Kolkata, India., Sasmal S; Department of Internal Medicine, KB Hostel, RG Kar Medical College, Room No. 1, Khudiram Bose Sarani, Kolkata, West Bengal 700004, India., Choudhury C; Department of Internal Medicine, Girls Hostel, RG Kar Medical College, Room No. 22, Khudiram Bose Sarani, Kolkata, West Bengal 700004, India., Mukhopadhyay S; RG Kar Medical College, Kolkata, India., Hajra A; Department of Internal Medicine, IPGMER, Kolkata, India., Layek M; Lady Hardinge Medical College, New Delhi, India., Karmakar PS; Department of Internal Medicine, RG Kar Medical College, Kolkata, India. |
Abstrakt: |
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 conditions may be coincidental. The antiphospholipid syndrome in patients with SLE may mimic the occlusive vasculitis of TA. |