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Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year old girl (CROSBI ID 211648)

Prilog u časopisu | kratko priopćenje | međunarodna recenzija

Jelušić, Marija ; Starčević, Katarina ; Dobrota, Savko ; Banfić. Ljiljana ; Potočki, kristina ; Anić, Branimir Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year old girl // Rheumatology international, 33 (2013), 5; 1359-1362. doi: 10.1007/s00296-011-2300-5

Podaci o odgovornosti

Jelušić, Marija ; Starčević, Katarina ; Dobrota, Savko ; Banfić. Ljiljana ; Potočki, kristina ; Anić, Branimir

engleski

Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year old girl

This article presents a case of a 17-year-old girl with primary antiphospholipid syndrome developing subacute signs of hand and leg ischaemia caused by radiologically verified radial and popliteal artery occlusion. She is successfully treated with a thrombolytic agent (alteplase) and recovers completely. Her laboratory results came positive for all three subtypes of antiphospholipid antibodies. This kind of antiphospholipid syndrome presentation is a very rare entity in itself. Shortly afterwards her mother is diagnosed with primary antiphospholipid syndrome as well. A familial form of antiphospholipid syndrome is suspected. Combination of a familial antiphospholipid syndrome presenting as bivessel arterial thrombosis is a unique case, to the best of our knowledge, never described in the literature before

antiphospholipid syndrome; familial

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Podaci o izdanju

33 (5)

2013.

1359-1362

objavljeno

0172-8172

10.1007/s00296-011-2300-5

Povezanost rada

Kliničke medicinske znanosti

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