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Antisynthetase Syndrome and Autoantibodies: A Literature Review and Report of 4 Cases

Identifieur interne : 000A71 ( Main/Exploration ); précédent : 000A70; suivant : 000A72

Antisynthetase Syndrome and Autoantibodies: A Literature Review and Report of 4 Cases

Auteurs : Flávia Luiza Marin [Brésil] ; Henrique Pereira Sampaio [Brésil]

Source :

RBID : PMC:6676984

Abstract

Case series

Patient: Female, 25 • Female, 39 • Male, 27 • Female, 42

Final Diagnosis: Antisynthetase syndrome

Symptoms: Arthralgia • dyspnea • muscle weakness

Medication: —

Clinical Procedure: Immunosuppressive therapy

Specialty: Rheumatology

Objective:

Rare disease

Background:

With the advent and advancement of autoantibodies, there has been progress in the diagnosis, prognosis, and treatment of rheumatologic diseases. Antisynthetase syndrome (ASS) is a great example of a disease that initially was described as arthritis, myositis, interstitial lung disease, mechanic’s hands, Raynaud’s phenomenon, and fever in the presence of the anti-JO-1 antibody, but nowadays it presents with a different spectrum related to new antibodies.

Case Report:

We describe 4 patients with antisynthetase syndrome who were diagnosed with antibodies specific for myositis associated with different clinical findings. All patients responded to immunosuppressive therapy, and rituximab was the most used.

Conclusions:

It is necessary to search for specific autoantibodies related to the syndrome in suspected clinical cases and in other rheumatological diseases refractory to the usual treatment.


Url:
DOI: 10.12659/AJCR.916178
PubMed: 31344020
PubMed Central: 6676984


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<nlm:aff id="af1-amjcaserep-20-1094">Postgraduate Program in Pathophysiology in Medical Clinic, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil</nlm:aff>
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<name sortKey="Sampaio, Henrique Pereira" sort="Sampaio, Henrique Pereira" uniqKey="Sampaio H" first="Henrique Pereira" last="Sampaio">Henrique Pereira Sampaio</name>
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<nlm:aff id="af2-amjcaserep-20-1094">Department of Rheumatology, Division of Medical Clinic, Section of Medicine, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil</nlm:aff>
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<bold>Case series</bold>
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<p>
<bold>Patient: Female, 25 • Female, 39 • Male, 27 • Female, 42</bold>
</p>
<p>
<bold>Final Diagnosis: Antisynthetase syndrome</bold>
</p>
<p>
<bold>Symptoms: Arthralgia • dyspnea • muscle weakness</bold>
</p>
<p>
<bold>Medication: —</bold>
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<p>
<bold>Clinical Procedure: Immunosuppressive therapy</bold>
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<bold>Specialty: Rheumatology</bold>
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<title>Objective:</title>
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<bold>Rare disease</bold>
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<title>Background:</title>
<p>With the advent and advancement of autoantibodies, there has been progress in the diagnosis, prognosis, and treatment of rheumatologic diseases. Antisynthetase syndrome (ASS) is a great example of a disease that initially was described as arthritis, myositis, interstitial lung disease, mechanic’s hands, Raynaud’s phenomenon, and fever in the presence of the anti-JO-1 antibody, but nowadays it presents with a different spectrum related to new antibodies.</p>
</sec>
<sec>
<title>Case Report:</title>
<p>We describe 4 patients with antisynthetase syndrome who were diagnosed with antibodies specific for myositis associated with different clinical findings. All patients responded to immunosuppressive therapy, and rituximab was the most used.</p>
</sec>
<sec>
<title>Conclusions:</title>
<p>It is necessary to search for specific autoantibodies related to the syndrome in suspected clinical cases and in other rheumatological diseases refractory to the usual treatment.</p>
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