Complete clinical and serological remission of anti-synthetase syndrome after autologous haematopoietic stem cell transplantation

Letters to the Editors Complete clinical and serological remission of anti-synthetase syndrome after autologous haematopoietic stem cell transplantationSirs, Anti-synthetase syndrome (ASS) is a chronic, rare, systemic autoimmune rheumatic disease.It is typically characterised by the presence of autoantibodies against different aminoacyl-transfer RNA synthetase (ARS), along with a range of clinical manifestations, including arthritis, myositis, skin involvement, and interstitial lung disease (ILD), among others (1).Management of ASS is often challenging due to disease heterogeneity, limited scientific evidence for treatment, and the lack of standardised guidelines (2).Long-term treatment is generally required.Severe cases carry an uncertain prognosis, although stabilisation or improvement is achievable.ILD progression

Authors

Institutions

Publication Details

Journal
Clinical and Experimental Rheumatology
Published
2026-02-24
DOI
https://doi.org/10.55563/clinexprheumatol/vezebx
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Complete clinical and serological remission of anti-synthetase syndrome after autologous haematopoietic stem cell transplantation

E Ruiz-Ortiz, Cristina Arnaldos, Virginia Ruiz-Esquide
Clinical and Experimental Rheumatology
Inflammatory Myopathies and Dermatomyositis
article

Complete clinical and serological remission of anti-synthetase syndrome after autologous haematopoietic stem cell transplantation

E Ruiz-Ortiz, Cristina Arnaldos, Virginia Ruiz-Esquide
article en

Abstract

Letters to the Editors Complete clinical and serological remission of anti-synthetase syndrome after autologous haematopoietic stem cell transplantationSirs, Anti-synthetase syndrome (ASS) is a chronic, rare, systemic autoimmune rheumatic disease.It is typically characterised by the presence of autoantibodies against different aminoacyl-transfer RNA synthetase (ARS), along with a range of clinical manifestations, including arthritis, myositis, skin involvement, and interstitial lung disease (ILD), among others (1).Management of ASS is often challenging due to disease heterogeneity, limited scientific evidence for treatment, and the lack of standardised guidelines (2).Long-term treatment is generally required.Severe cases carry an uncertain prognosis, although stabilisation or improvement is achievable.ILD progression

Clinical and Experimental RheumatologyVol. 44(2)
Hospital Clínic de Barcelona (ES)
Good health and well-being
Openalex Percentile: Top 45%
Inflammatory Myopathies and Dermatomyositis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.