Artigo Acesso aberto Revisado por pares

Anti-PL-7 Antisynthetase Syndrome with Eosinophilic Pleural Effusion

2018; The Japanese Society of Internal Medicine; Volume: 57; Issue: 15 Linguagem: Inglês

10.2169/internalmedicine.0302-17

ISSN

1349-7235

Autores

Go Saito, Masato Kono, Akari Tsutsumi, Yu Koyanagi, Koichi Miyashita, Takeshi Kobayashi, Hironao Hozumi, Yoshihiro Miki, Yoshifumi Arai, Yoshiro Otsuki, Dai Hashimoto, Tomoyuki Fujisawa, Tõru Nakamura, Takafumi Suda, Hidenori Nakamura,

Tópico(s)

Muscle and Compartmental Disorders

Resumo

A 68-year-old woman was admitted to our hospital with fever and pleural effusion. Her thoracentesis showed eosinophilic pleural effusion (EPE) without any evidence of malignancy, infection, or trauma. Pleural biopsy revealed pleuritis and intercostal myositis. Characteristic skin manifestations, including Gottron's sign, interstitial lung disease, and pericardial effusion, appeared later in the clinical course. She was finally diagnosed with anti-PL-7 antisynthetase syndrome (ASS) based on the presence of anti-PL-7 antibody, and she fulfilled the diagnostic criteria for dermatomyositis. These clinical manifestations improved with immunosuppressive therapy. EPE might therefore be one of the characteristic features of anti-PL-7 ASS.

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