A case of interstitial pneumonia associated with anti-PL-7 antibody in a patient with rheumatoid arthritis
Autor: | Hisatsugu Goto, Yasuhiko Nishioka, Mayo Kondo, Hiroyuki Kozai, Jun Kishi, Hiroshi Kawano, Yuya Yamashita, Haruka Nishimura, Yuko Toyoda, Makoto Tobiume |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
rheumatoid arthritis
medicine.medical_specialty Exacerbation medicine.drug_class Gastroenterology General Biochemistry Genetics and Molecular Biology Amino Acyl-tRNA Synthetases Arthritis Rheumatoid 03 medical and health sciences 0302 clinical medicine Internal medicine Medicine Humans Myositis anti-PL-7antibody Aged Autoantibodies 030203 arthritis & rheumatology interstitial pneumonia Lung business.industry General Medicine medicine.disease medicine.anatomical_structure anti-aminoacyl tRNA synthetase antibody syndrome 030228 respiratory system Rheumatoid arthritis Etiology Prednisolone Corticosteroid Female business Lung Diseases Interstitial Nephrotic syndrome medicine.drug |
Zdroj: | The Journal of Medical Investigation. 65(1-2):147-150 |
ISSN: | 1349-6867 |
Popis: | A 65-year-old female had been treated rheumatoid arthritis (RA), interstitial pneumonia (IP) and nephrotic syndrome with prednisolone and cyclosporine. She was emergently admitted to our hospital due to the worsening exertional dyspnea and severe hypoxemia. Chest computed tomography (CT) showed new diffuse ground-glass opacities (GGOs) with slight consolidations along with bronchovascular bundle were observed in addition to pre-existing reticular shadows in both lungs with lower lobe-predominance. An acute exacerbation (AE) of pre-existing IP triggered by an infection was suspected, and the treatment with antibiotics and corticosteroid pulse therapy improved her general condition and chest radiological findings. Because some auto-antibodies associated with acute/subacute onset IP have recently become available in clinic, we examined those including anti-aminoacyl tRNA synthetase (ARS) antibodies, and found that she was positive for anti-PL-7 antibody. We diagnosed her anti-synthetase syndrome (ASS) without symptom of myositis, and her IP was considered to be ASS-related. The careful consideration is necessary to precisely diagnose and treat the patients with RA-associated interstitial lung diseases as the several etiologies may be overlapped in the same patient. J. Med. Invest. 65:147-150, February, 2018. |
Databáze: | OpenAIRE |
Externí odkaz: |