Abstract |
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.
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Authors | Marija Jelušić, Katarina Starčević, Mandica Vidović, Savko Dobrota, Kristina Potočki, Ljiljana Banfić, Branimir Anić |
Journal | Rheumatology international
(Rheumatol Int)
Vol. 33
Issue 5
Pg. 1359-62
(May 2013)
ISSN: 1437-160X [Electronic] Germany |
PMID | 22190275
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Antibodies, Antiphospholipid
- Anticoagulants
- Biomarkers
- Fibrinolytic Agents
- Warfarin
- Tissue Plasminogen Activator
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Topics |
- Administration, Oral
- Adolescent
- Angiography, Digital Subtraction
- Antibodies, Antiphospholipid
(blood)
- Anticoagulants
(administration & dosage)
- Antiphospholipid Syndrome
(blood, complications, diagnosis, genetics, immunology)
- Arterial Occlusive Diseases
(blood, diagnosis, drug therapy, etiology)
- Biomarkers
(blood)
- Constriction, Pathologic
- Female
- Fibrinolytic Agents
(therapeutic use)
- Genetic Predisposition to Disease
- Heredity
- Humans
- Ischemia
(etiology)
- Pedigree
- Popliteal Artery
(diagnostic imaging)
- Radial Artery
(diagnostic imaging)
- Thrombolytic Therapy
- Tissue Plasminogen Activator
(therapeutic use)
- Treatment Outcome
- Warfarin
(administration & dosage)
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