Abstract
Antisynthetase syndrome is a subtype of idiopathic inflammatory myopathy, strongly associated with the presence of interstitial lung disease. Diagnosis is made by identifying myositis-specific antibodies directed against aminoacyl tRNA synthetase, and relevant clinical and radiologic features. Given the multisystem nature of the disease, diagnosis requires the careful synthesis of subtle clinical and radiological features with the interpretation of specialized autoimmune serological testing. This is provided in a multidisciplinary environment with input from rheumatologists, respiratory physicians, and radiologists. Differentiation from other idiopathic interstitial lung diseases is key; treatment and prognosis differ between patients with antisynthetase syndrome and idiopathic interstitial lung disease. In this review article, we look at the role of the multidisciplinary team and its individual members in the initial diagnosis of the antisynthetase syndrome, including the role of physicians, radiologists, and the wider team.
| Original language | English |
|---|---|
| Article number | 959653 |
| Number of pages | 14 |
| Journal | Frontiers in Medicine |
| Volume | 9 |
| DOIs | |
| Publication status | Published - 14 Sept 2022 |
Bibliographical note
Funding Information:Funding for the publication of this article has been kindly provided by the Bristol Interstitial Lung Disease Research Fund.
Funding Information:
The authors thank Sarah Rudd, librarian, North Bristol NHS Trust and also Dr Chan and Dr Andrade of ANApatterns.org.
Publisher Copyright:
Copyright © 2022 Wells, Alawi, Thin, Gunawardena, Brown, Edey, Pauling, Barratt and Adamali.