ArticleCureus2025
A Clinical Case of Thymoma Presenting With Pure Erythroid Aplasia.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Pure Red Cell Aplasia as an Isolated Paraneoplastic Manifestation of Thymoma: A Case Report and Literature Review.Clinical case reports · 2026Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Thymic tumors are a rare condition that affects both genders equally, typically presenting between the ages of 40 and 70. Although often asymptomatic, they can give rise to paraneoplastic syndromes, with myasthenia gravis being the most common. The presentation of pure red cell aplasia, however, remains an uncommon manifestation. Thymectomy is the primary treatment, but it may not always be sufficient for managing associated syndromes, and immunosuppressive therapy may be necessary. This case involves a 50-year-old, otherwise healthy man, who presented to the emergency department with progressive dyspnea and asthenia over the course of one month. A mediastinal mass and hypoproliferative normocytic, normochromic anemia were identified, and after a diagnostic work-up, it was concluded to be a case of thymoma with associated pure red cell aplasia. The patient underwent surgery and radiotherapy and received immunosuppressive therapy. This case highlights a rare manifestation of an uncommon pathology, underscoring the need for a multidisciplinary approach and the challenges in treatment.
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Registered trials
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