Myasthenia gravis and paroxysmal nocturnal hemoglobinuria after thymectomy: A rare association.
Jean GaltierFanny DuvalIrène MachelartCarine GreibEstibaliz LazaroJean-Luc PellegrinJean-François ViallardRegis Peffault de la TourEtienne RivièrePublished in: EJHaem (2021)
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.
Keyphrases
- myasthenia gravis
- bone marrow
- atrial fibrillation
- chronic kidney disease
- obstructive sleep apnea
- multiple sclerosis
- allogeneic hematopoietic stem cell transplantation
- mesenchymal stem cells
- case report
- pulmonary embolism
- sleep apnea
- iron deficiency
- physical activity
- acute myeloid leukemia
- sleep quality
- catheter ablation