https://doi.org/10.4081/reumatismo.2017.923

First report of anti-TIF1γ dermatomyositis in a patient with myelodysplastic syndrome

Vol. 69 No. 2 (2017)
Submitted: 10 September 2016
Accepted: 27 April 2017
Published: 3 August 2017
Myelodisplastic syndrome, Myositis specific autoantibodies, Anti-TIF1γ, Dermatomyositis.
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Authors

B. Palterer
Experimental and Clinical Medicine Dept., University of Florence, Florence, Italy.
G. Vitiello
gianfranco.vitiello@unifi.it
Experimental and Clinical Medicine Dept., University of Florence, Florence, Italy.
D. Cammelli
Rheumatology Section/Immunoallergology Unit, AOU-Careggi, Florence, Italy.
Inflammatory myopathies as para-neoplastic phenomena were first described by Sterz in 1916. Recently, myositis specific autoantibodies were described in cancer-associated myositis. Anti-transcription intermediary factor 1 gamma (anti-TIF1γ) antibodies have been found in both young adults affected by juvenile dermatomyositis and in elderly patients with cancer-associated myositis. In this regard, we report herein the first case of anti-TIF1γ dermatomyositis secondary to a myelodysplastic syndrome.

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Supporting Agencies

-
B. Palterer, Experimental and Clinical Medicine Dept., University of Florence, Florence
Resident in Allergy and Clinical Immunology
G. Vitiello, Experimental and Clinical Medicine Dept., University of Florence, Florence
Resident in Allergy and Clinical Immunology
D. Cammelli, Rheumatology Section/Immunoallergology Unit, AOU-Careggi, Florence
Head of the Reumatology Section of the Immunoallergology Unit

How to Cite

Palterer, B., Vitiello, G., & Cammelli, D. (2017). First report of anti-TIF1γ dermatomyositis in a patient with myelodysplastic syndrome. Reumatismo, 69(2), 75–77. https://doi.org/10.4081/reumatismo.2017.923

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