Mechanic's hands in a woman with undifferentiated connective tissue disease and interstitial lung disease - Anti-PL7 positive antisynthetase syndrome: A case report

被引:3
作者
De Langhe E. [1 ]
Lenaerts J. [1 ]
Bossuyt X. [2 ]
Westhovens R. [1 ]
Wuyts W.A. [3 ]
机构
[1] Department of Rheumatology, University Hospitals Leuven, Herestraat 49, Leuven
[2] Department of Laboratory Medicine, University Hospitals Leuven, Herestraat 49, Leuven
[3] Department of Pulmonary Medicine, University Hospitals Leuven, Herestraat 49, Leuven
关键词
Antisynthetase syndrome; Connective tissue diseases; Dermatomyositis; Pulmonary fibrosis;
D O I
10.1186/s13256-015-0571-2
中图分类号
学科分类号
摘要
Introduction: Interstitial lung disease can be idiopathic or occur in the setting of connective tissue diseases. In the latter case it requires a different treatment approach with a better prognosis. Interstitial lung disease can precede the onset of typical connective tissue disease features by many years, and therefore meticulous multidisciplinary follow-up is crucial. This case highlights the diagnostic challenge and the need for intensified attention for subtle clinical features when faced with interstitial lung disease in patients with characteristics of a hitherto undifferentiated connective tissue disease. Case presentation: A 44-year-old Caucasian woman presented to our pulmonology department with dyspnea, Raynaud's phenomenon and subtle swelling of fingers and eyelids. Laboratory analysis and autoantibody screening was negative. She was diagnosed with nonspecific interstitial pneumonia with a concurring undifferentiated connective tissue disease. After four years of stable disease, she presented with rapid pulmonary deterioration, myalgia, periorbital edema, arthritis and a cracked appearance of the radial sides of the fingers of both her hands. This clinical sign was recognized as mechanic's hands and a specific search for the presence of antisynthetase antibodies was performed. She was found to harbor anti-threonyl-tRNA synthetase antibodies. A diagnosis of antisynthetase syndrome was made and she was treated with glucocorticoids and immunosuppressives. Conclusions: This case highlights the difficulty in fine-tuning the diagnosis when confronted with a patient with interstitial lung disease and the suspicion of an underlying, yet undifferentiated connective tissue disease. There is a strong need for clinical multidisciplinary follow-up of these patients, with a high level of alertness to rare and specific clinical signs. The diagnosis of the underlying connective tissue disease profoundly influences the management of the interstitial lung disease. Recent data stress that identification of the autoantibody specificity allows for further prognostic stratification and therefore should be pursued. © 2015 De Langhe et al.; licensee BioMed Central.
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共 14 条
[1]  
Park J.H., Kim D.S., Park I.N., Jang S.J., Kitaichi M., Nicholson A.G., Et al., Prognosis of fibrotic interstitial pneumonia: Idiopathic versus collagen vascular disease-related subtypes, Am J Respir Crit Care Med., 175, pp. 705-711, (2007)
[2]  
Tillie-Leblond I., Wislez M., Valeyre D., Crestani B., Rabbat A., Israel-Biet D., Et al., Interstitial lung disease and anti-Jo-1 antibodies: Difference between acute and gradual onset, Thorax., 63, pp. 53-59, (2008)
[3]  
Lega J.C., Fabien N., Reynaud Q., Durieu I., Durupt S., Dutertre M., Et al., The clinical phenotype associated with myositis-specific and associated autoantibodies: A meta-analysis revisiting the so-called antisynthetase syndrome, Autoimmun Rev, 13, 9, pp. 883-891, (2014)
[4]  
Labirua-Iturburu A., Selva-O'Callaghan A., Vincze M., Danko K., Vencovsky J., Fisher B., Et al., Anti-PL-7 (anti-threonyl-tRNA synthetase) antisynthetase syndrome: Clinical manifestations in a series of patients from a European multicenter study (EUMYONET) and review of the literature, Medicine (Baltimore), 91, pp. 206-211, (2012)
[5]  
Marie I., Josse S., Decaux O., Diot E., Landron C., Roblot P., Et al., Clinical manifestations and outcome of anti-PL7 positive patients with antisynthetase syndrome, Eur J Intern Med., 24, pp. 474-479, (2013)
[6]  
Hervier B., Benveniste O., Clinical heterogeneity and outcomes of antisynthetase syndrome, Curr Rheumatol Rep., 15, (2013)
[7]  
Mahler M., Miller F.W., Fritzler M.J., Idiopathic inflammatory myopathies and the anti-synthetase syndrome: A comprehensive review, Autoimmun Rev., 13, pp. 367-371, (2014)
[8]  
Aggarwal R., Cassidy E., Fertig N., Koontz D.C., Lucas M., Ascherman D.P., Et al., Patients with non-Jo-1 anti-tRNA-synthetase autoantibodies have worse survival than Jo-1 positive patients, Ann Rheum Dis., 73, pp. 227-232, (2014)
[9]  
Hervier B., Devilliers H., Stanciu R., Meyer A., Uzunhan Y., Masseau A., Et al., Hierarchical cluster and survival analyses of antisynthetase syndrome: Phenotype and outcome are correlated with anti-tRNA synthetase antibody specificity, Autoimmun Rev., 12, pp. 210-217, (2012)
[10]  
Marie I., Josse S., Decaux O., Dominique S., Diot E., Landron C., Et al., Comparison of long-term outcome between anti-Jo1- and anti-PL7/PL12 positive patients with antisynthetase syndrome, Autoimmun Rev., 11, pp. 739-745, (2012)