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Clin Rheumatol ; 43(8): 2701-2705, 2024 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-38970750

RESUMEN

Aplastic anemia is a rare and heterogeneous disease that causes pancytopenia and aplasia of the bone marrow. It is characterized by a failure of hematopoiesis. It is believed that approximately 65% of cases of acquired aplastic anemia are idiopathic. In a subset of cases, a drug or infection is the cause of bone marrow failure. This case report presents a 38-year-old patient with axial spondylarthritis who developed pancytopenia and was diagnosed with aplastic anemia during anti-TNF-α treatment.


Asunto(s)
Anemia Aplásica , Pancitopenia , Factor de Necrosis Tumoral alfa , Humanos , Adulto , Pancitopenia/inducido químicamente , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores , Anemia Aplásica/inducido químicamente , Masculino , Espondiloartritis/tratamiento farmacológico , Espondiloartritis/complicaciones , Antirreumáticos/efectos adversos , Espondiloartritis Axial/inducido químicamente , Infliximab/efectos adversos , Infliximab/uso terapéutico
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