Anti-Synthetase Syndrome-Related Interstitial Lung Disease With Anti-PL-12 Antibodies

被引:5
作者
Elferjani, Belqis [1 ]
Liaqat, Adnan [1 ]
Zaman, Mohammed [1 ]
Sexton, Marvin [2 ]
机构
[1] Southeast Hlth Med Ctr, Internal Med, Dothan, AL 36301 USA
[2] Dothan Pulm Associates, Pulmonol, Dothan, AL USA
关键词
anti-synthetase syndrome; interstitial lung disease; anti-pl-12; antibody; INFLAMMATORY MYOPATHY; AUTOANTIBODIES;
D O I
10.7759/cureus.12936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anti-synthetase syndrome usually comprises interstitial lung disease, myositis, arthralgias, and Raynaud phenomenon. The anti-PL-12 antibody is directed against the enzyme alanyl-tRNA synthetase and has been associated with interstitial lung disease in the absence of inflammatory myositis. We report the case of a 33-year-old woman with complaints of progressive dyspnea, a persistent dry cough, along with intermittent low-grade fever for a few months. A computed tomography (CT) scan of the chest showed the presence of patchy bilateral airspace opacities and infiltrates. It also showed significant mediastinal and hilar lymphadenopathy. Bronchoscopy with transbronchial biopsy was performed, and histopathology changes were consistent with connective tissue disease related to interstitial lung disease. Further workup revealed the presence of anti-PL-12 antibodies. This case illustrates a rare association of interstitial lung disease with the anti-PL-12 antibody.
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页数:5
相关论文
共 11 条
[1]   Interstitial Lung Disease Associated With the Idiopathic Inflammatory Myopathies What Progress Has Been Made in the Past 35 Years? [J].
Connors, Geoffrey R. ;
Christopher-Stine, Lisa ;
Oddis, Chester V. ;
Danoff, Sonye K. .
CHEST, 2010, 138 (06) :1464-1474
[2]   A 64-year-old woman with interstitial lung disease and positive antibodies against aminoacyl-transfer RNA synthetases in the absence of myositis: presentation of an anti-PL-12 positive antisynthetase syndrome [J].
Ghysen, Katrien ;
Leys, Mathias .
ACTA CLINICA BELGICA, 2018, 73 (05) :389-392
[3]   Pulmonary Manifestations of the Idiopathic Inflammatory Myopathies [J].
Kalluri, Meena ;
Oddis, Chester V. .
CLINICS IN CHEST MEDICINE, 2010, 31 (03) :501-+
[4]   Antisynthetase Syndrome [J].
Katzap, Elena ;
Barilla-LaBarca, Maria-Louise ;
Marder, Galina .
CURRENT RHEUMATOLOGY REPORTS, 2011, 13 (03) :175-181
[5]   A NEW APPROACH TO THE CLASSIFICATION OF IDIOPATHIC INFLAMMATORY MYOPATHY - MYOSITIS-SPECIFIC AUTOANTIBODIES DEFINE USEFUL HOMOGENEOUS PATIENT GROUPS [J].
LOVE, LA ;
LEFF, RL ;
FRASER, DD ;
TARGOFF, IN ;
DALAKAS, M ;
PLOTZ, PH ;
MILLER, FW .
MEDICINE, 1991, 70 (06) :360-374
[6]   POLYMYOSITIS, PULMONARY FIBROSIS AND AUTOANTIBODIES TO AMINOACYL-TRANSFER RNA-SYNTHETASE ENZYMES [J].
MARGUERIE, C ;
BUNN, CC ;
BEYNON, HLC ;
BERNSTEIN, RM ;
HUGHES, JMB ;
SO, AK ;
WALPORT, MJ .
QUARTERLY JOURNAL OF MEDICINE, 1990, 77 (282) :1019-1038
[7]   ANTI-THREONYL-TRNA SYNTHETASE, A 2ND MYOSITIS-RELATED AUTOANTIBODY [J].
MATHEWS, MB ;
REICHLIN, M ;
HUGHES, GRV ;
BERNSTEIN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (02) :420-434
[8]  
Satoh S, 1996, Ryumachi, V36, P862
[9]   Dermatomyositis with Rapidly Progressive Interstitial Lung Disease Treated with Rituximab: A Report of 3 Cases in Japan [J].
Tokunaga, Kenichiro ;
Hagino, Noboru .
INTERNAL MEDICINE, 2017, 56 (11) :1399-1403
[10]   Characteristics of interstitial lung disease in SS-A positive/Jo-1 positive inflammatory myopathy patients [J].
Vancsa, Andrea ;
Csipo, I. ;
Nemeth, J. ;
Devenyi, K. ;
Gergely, L. ;
Danko, K. .
RHEUMATOLOGY INTERNATIONAL, 2009, 29 (09) :989-994