ArticleEJHaem2021
Myasthenia gravis and paroxysmal nocturnal hemoglobinuria after thymectomy: A rare association.
Article in EJHaem, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
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Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Clinical characteristics and treatment outcomes in thymoma- related aplastic anemia: a case report and literature review.Journal of cardiothoracic surgery · 2026Pooled it
- Aplastic Anemia Proceeding to Thymoma: A Rare Co-Occurrence-A Case Report and Review Article.Case reports in hematology · 2026Article
- Eculizumab Treatment of Massive Hemolysis Occurring in a Rare Co-Existence of Paroxysmal Nocturnal Hemoglobinuria and Myasthenia Gravis.Hematology reports · 2024Article
- Myasthenia gravis and paroxysmal nocturnal hemoglobinuria after thymectomy: A rare association.EJHaem · 2021Article
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Authors and funding
9 authors.
Funding
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Abstract
Paroxysmal nocturnal hemoglobinuria (PNH) is a very rare clonal autoimmune disease manifesting with hemolysis, thrombosis, or bone marrow failure. We present an atypical association of myasthenia gravis, aplastic anemia, and PNH occurring years after thymectomy. While this association might be extremely rare, it may not be coincidental as there is a common pathophysiology between PNH and aplastic anemia, with the latter reported in several thymoma/thymectomy cases. Eculizumab was introduced with good efficacy and without safety concern in our patient, leading to long-term control of PNH without worsening of myasthenia gravis.
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