Evidence map›Paper›PMID 42005993›Full record

ArticleCase reports in rheumatology2026

Thymoma-Associated Systemic Lupus Erythematosus and Myasthenia Gravis.

Keysha González-Ramos, Ileana Rivera-Burgos, Carlos Cedeño, Jean Lafontaine, María J Marcos-Martínez, Luis M Vilá

Abstract read
In one paragraph

Article in Case reports in rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Keysha González-RamosDivision of Rheumatology, Department of Medicine, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico, USA.ORCID https://orcid.org/0000-0003-1777-5585
Ileana Rivera-BurgosDivision of Rheumatology, Department of Medicine, Hospital Damas, Ponce, Puerto Rico, USA.
Carlos CedeñoDivision of Hematology, Medical Oncology, Department of Medicine, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico, USA.
Jean LafontaineDepartment of Pathology and Laboratory Medicine, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico, USA, lhsc.on.ca.
María J Marcos-MartínezDepartment of Pathology and Laboratory Medicine, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico, USA, lhsc.on.ca.
Luis M ViláDivision of Rheumatology, Department of Medicine, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, Puerto Rico, USA.ORCID https://orcid.org/0000-0002-6679-2704

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymomas, rare tumors originating from thymic epithelial cells, can disrupt immune tolerance and contribute to the development of autoimmune diseases. While thymomas are commonly associated with myasthenia gravis (MG), their link to autoimmune rheumatic diseases such as systemic lupus erythematosus (SLE) is less frequently observed. We present a case of a 32-year-old woman with SLE who was admitted with headache, blurred vision in her right eye with ptosis, generalized weakness, and dysphagia. She had been experiencing dysphagia and weakness for the past year, with symptoms intensifying in the three weeks leading up to admission. Her SLE had been diagnosed a year earlier, presenting with polyarthritis, positive antinuclear and anti-dsDNA antibodies, and low levels of C3 and C4. Inpatient laboratories revealed positive anti-acetylcholine receptor antibodies. A chest computed tomography (CT) scan revealed an anterior mediastinal mass invading the left pleural space as well as the left brachial and cephalic veins. A CT-guided biopsy of the mass confirmed a thymoma consistent with World Health Organization type AB. She was diagnosed with MG and thymoma. MG was managed with prednisone, pyridostigmine, and intravenous immunoglobulin. She underwent four cycles of neoadjuvant chemotherapy for her thymoma, with two additional cycles, with a modified treatment regimen, administered to enhance tumor reduction prior to surgery. She underwent thymectomy, pericardiectomy, venorrhaphy, and pneumorrhaphy and was initiated on radiation therapy due to tumor invasion of adjacent structures. At 12-month follow-up, her MG symptoms had completely resolved. As for her SLE, arthralgias persisted in the absence of arthritis, and no additional lupus manifestations developed. This case illustrates the diagnostic challenges posed by overlapping autoimmune disorders and emphasizes the need for careful evaluation to identify underlying malignancies, like thymoma, in patients presenting with atypical or evolving autoimmune symptoms.

Identifiers

PMID42005993
PMCPMC13084321

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