Impaired production [1][2][3]
Nutritional deficiencies, e.g.:
Vitamin B12 deficiency
Folate deficiency
Copper deficiency
Aplastic anemia etiologies
Acquired, e.g.:
Idiopathic
Radiation injury
Alcohol use disorder
Medications,
Viral, bacterial, or parasitic infections
Sepsis
Inherited bone marrow failure disorders, e.g., Fanconi anemia
Malignant bone marrow infiltration
Acute leukemia, e.g.:
Acute myeloid leukemia (AML)
Acute promyelocytic leukemia (APL)
Acute lymphoblastic leukemia (ALL)
Other myeloid neoplasms, e.g.:
Myelodysplastic syndromes (MDS)
Myelofibrosis
Chronic myeloid leukemia (CML)
Multiple myeloma
Lymphoproliferative disorders, e.g.:
Low-grade non-Hodgkin lymphomas with marrow involvement
Hodgkin lymphoma
Hairy cell leukemia
Marrow infiltration by solid organ malignancy, e.g.:
Lung cancer,
Breast cancer
Prostate cancer
Nonmalignant bone marrow infiltration, e.g.:
Gaucher disease
TB
Leishmaniasis
Increased destruction or loss [1][2]
Autoimmune, e.g.: autoimmune hemolytic pancytopenia
Thrombotic microangiopathies, e.g.: disseminated intravascular coagulation (DIC)
Splenic sequestration, e.g.: due to portal hypertension
Impaired production and increased destruction [2]
Medications, e.g.: [3]
Antibiotics, e.g., chloramphenicol, trimethoprim
Antiepileptic drugs, e.g., carbamazepine, valproate
Chemotherapeutic agents
Immunosuppressants, e.g., azathioprine, methotrexate
Infections, e.g.:
Malaria
Schistosomiasis
Viral infections
Autoimmune conditions: e.g., systemic lupus erythematosus (SLE), rheumatoid arthritis
Other, e.g.:
Hemophagocytic lymphohistiocytosis (HLH), e.g., due to viral infection
Paroxysmal nocturnal hemoglobinuria (PNH)
Transfusion-associated graft-versus-host