Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 Jun 13;15(6):e40354.
doi: 10.7759/cureus.40354. eCollection 2023 Jun.

Antisynthetase Syndrome With Paraneoplastic Antibodies

Affiliations
Case Reports

Antisynthetase Syndrome With Paraneoplastic Antibodies

Ashbina Pokharel et al. Cureus. .

Abstract

Antisynthetase syndrome (ASyS) is an uncommon systemic autoimmune disorder characterized by the presence of autoantibodies targeting aminoacyl-transfer RNA (tRNA) synthetase. The syndrome displays a diverse range of clinical manifestations affecting multiple organs, thereby posing a diagnostic challenge. In this report, we present an unusual case of a patient diagnosed with ASyS, displaying positive anti-PL-12 antibodies along with paraneoplastic antibodies. To the best of our knowledge, this is the first documented case in the existing literature describing ASyS with the presence of anti-PL-12 antibodies and concomitant paraneoplastic antibodies in the context of ductal carcinoma in situ.

Keywords: antisynthetase syndrome; autoimmune disease; ductal carcinoma in-situ; interstitial lung disease; paraneoplastic syndrome.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Facial erythematous rash with scaling.
Figure 2
Figure 2. The patient’s right hand with bluish discoloration of fingers, hyperkeratosis, and scaling of the radial aspect of the second finger.
Figure 3
Figure 3. CT chest demonstrating interstitial lung disease which appears slightly worsened with possible developing honeycombing at the bases, superimposed ground glass opacities within the lung bases, right middle lobe, and lingula.

References

    1. Anti-synthetase syndrome: a rare and challenging diagnosis for bilateral ground-glass opacities-a case report with literature review. Alfraji N, Mazahir U, Chaudhri M, Miskoff J. BMC Pulm Med. 2021;21:11. - PMC - PubMed
    1. Interstitial lung disease associated with the idiopathic inflammatory myopathies: what progress has been made in the past 35 years? Connors GR, Christopher-Stine L, Oddis CV, Danoff SK. Chest. 2010;138:1464–1474. - PubMed
    1. Myositis-related interstitial lung disease and antisynthetase syndrome. Solomon J, Swigris JJ, Brown KK. J Bras Pneumol. 2011;37:100–109. - PMC - PubMed
    1. Hematological malignancy associated with polymyositis and dermatomyositis. Marie I, Guillevin L, Menard JF, et al. Autoimmun Rev. 2012;11:615–620. - PubMed
    1. A longitudinal cohort study of the anti-synthetase syndrome: increased severity of interstitial lung disease in black patients and patients with anti-PL7 and anti-PL12 autoantibodies. Pinal-Fernandez I, Casal-Dominguez M, Huapaya JA, et al. Rheumatology (Oxford) 2017;56:999–1007. - PMC - PubMed

Publication types

LinkOut - more resources