Secondary antiphospholipid syndrome revealed by the sudden onset of pneumonia: Case report
| Autor: | Vladimir Zugic, Mirjana Zlatkovic-Svenda, Dzemail S Detanac, Jelena Kovac, Dzenana A Detanac, Sanja Sarac, Ivana Blazic, Biljana Lazovic, Rade Milic |
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| Rok vydání: | 2019 |
| Předmět: |
lcsh:R5-920
medicine.medical_specialty business.industry Pleural effusion autoimmunity Context (language use) medicine.disease medicine.disease_cause Thrombosis Dermatology 3. Good health Autoimmunity Pneumonia systemic lupus erythematosus secondary antiphospholipid syndrome immune system diseases medicine antibodies In patient lcsh:Medicine (General) skin and connective tissue diseases business thrombosis Secondary antiphospholipid syndrome Sudden onset |
| Zdroj: | Sanamed, Vol 14, Iss 3, Pp 287-290 (2019) |
| ISSN: | 2217-8171 1452-662X |
| Popis: | Introduction: Secondary antiphospholipid syndrome (SAPS) is APS that occurs in the context of another medical condition. Although antiphospholipid antibodies (aPL) can occur in patients with viral, bacterial, or protozoal infections, they are rarely associated with thrombosis. Aim: To present an uncommon case of pneumonia and pleural effusion complicated with pulmonary thromboembolism in a patient with systemic lupus erythematosus (SLE), due to non-diagnosed secondary antiphospholipid syndrome. Case report: A 28 years old woman, never pregnant, with a family history of systemic lupus erythematosus, has been suffering from SLE from the age of 18. She had only articular and skin manifestations, without internal organ involvement. She has been taking Methotrexate (10 mg weekly) and Prednisone (5 mg daily) in the previous 10 years. She was presented at the Emergency department with the radiological finding of pleuropneumonia followed by temperature up to 39C, shortness of breath, cough, fatigue, and weakness. Results: She was treated initially with three antibiotics and thoracocentesis. She developed pulmonary thrombosis without deep venous thrombosis. Laboratory findings were: ESR = 37 mm/h, CRP = 2+, ANA = 1/80 peripheral, RF negative, anti-dsDNA = 147 (positive > 40), anti-Sm negative, anticardiolipin IgG antibody 158 GPL (up to 12), anticardiolipin IgM antibody 5.5 MPL (up to 10), anti-beta2-glycoprotein IgG and IgM were negative and lupus anti-coagulant was 88" (18"-55"). The patient underwent Heparin and Warfarin treatment, by checking INR to be in a 2.6 to 3.5 range. Prednisolone and Hydroxychloroquine were also started. Conclusion: All patients suspected with SLE should be evaluated for antiphospholipid antibodies (APL). However, APS diagnosis requires both clinical and laboratory features. |
| Databáze: | OpenAIRE |
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