PATIENTS WITH ELEVATED CREATINE KINASE LEVELS IN RHEUMATOLOGY OUTPATIENT CLINIC – CASE SERIES
| Autor: | BAREŠIĆ, MARKO, RUKAVINA, KREŠIMIR, PADJEN, IVAN, ŽARKOVIĆ, KAMELIJA, ANIĆ, BRANIMIR |
|---|---|
| Jazyk: | chorvatština |
| Rok vydání: | 2017 |
| Předmět: |
Creatine kinase – blood
polymyositis – diagnosis therapy Dermatomyositis – diagnosis therapy Electromyography Muscle sceletal – pathology Biopsy Kreatin kinaza – u krvi Polimiozitis – diagnoza liječenje Dermatomiozitis – dijagnoza liječenje Elektromiografija Skeletni mišići – patologija Biopsija Skeletni |
| Zdroj: | Liječnički vjesnik Volume 139 Issue 5-6 |
| ISSN: | 0024-3477 1849-2177 |
| Popis: | Kreatin kinaza (CK) enzim je koji dovodi do pretvorbe kreatina u kreatin fosfat te se nalazi u različitim tkivima tijela. Kliničku važnost ima CK podrijetlom iz mišića jer je biljeg oštećenja mišića različitim uzrocima. Povišene vrijednosti CK učestali su razlog upućivanja bolesnika reumatologu pod sumnjom na upalnu idiopatsku miopatiju. U tekstu su analizirani podaci dobiveni promatranjem skupine bolesnika upućenih u polikliničku ambulantu u razdoblju od dvije godine. Analizirani su podaci za ukupno 23 bolesnika (16 žena i 7 muškaraca), u dobi između 31 i 78 godina (prosječne dobi 53,43 godine). Upalna bolest mišića utvrđena je u 13/23 (56,52%) bolesnika (polimiozitis u 76,92%, a dermatomiozitis u 23,08%). Liječenje je uz nefarmakološke mjere uključivalo glukokortikoide i kombinaciju s imunosupresivima i/ili imunomodulatorima (azatioprin, metotreksat, antimalarik i intravenski imunoglobulini). Creatine kinase (CK) is an enzyme found in different tissues and is responsible for the conversion of creatine into phosphocreatine. Muscle-derived CK has clinical significance as a marker of muscle injury. Elevated levels of CK are a frequent reason for referring the patient with suspected inflammatory idiopathic myopathies to the Rheumatology outpatient clinic. We analyzed the data from 23 referred patients collected over the period of two years. The analyzed data were collected from 16 female and 7 male patients aged 31 to 78 (with the average age of 53.43 years). Inflammatory idiopathic myopathies were confirmed in 13/23 (56.52%) patients (polymyositis in 76,92% and dermatomyositis in 23.08%). The treatment included nonpharmacological modalities and different immunosuppressive and/or immunomodulatory drugs (glucocorticoids, azathioprine, methotrexate, antimalarials and intravenous immunoglobulines). |
| Databáze: | OpenAIRE |
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