Differential diagnosis of neutropenia.
Acquired . |
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Table adapted from: Newburger PE. Neutropenia. In: Rakel RE, Bope ET, eds. Conn’s Current Therapy 2006. Philadelphia: Saunders Elsevier; 2006:502–505 |
Bone marrow aplasia, dysplasia, or replacement |
Drug-induced |
impaired production (chemotherapy, phenothiazines, other drugs) |
antibody-mediated (aminopyrine, other drugs) |
Hypersplenism |
Immune-mediated (alloimmune and autoimmune) |
Nutritional (folate, vitamin B12) |
Sepsis with exhaustion of bone marrow storage pool |
Viral bone marrow suppression |
Congenital |
Cyclic hematopoiesis |
Familial benign neutropenia |
Myelokathexis |
Severe chronic neutropenia |
Complex syndromes including neutropenia |
Cartilage-hair hypoplasia |
Chédiak-Higashi syndrome |
Dyskeratosis congenital |
Primary immunodeficiencies (e.g., X-linked hyper-IgM syndrome) |
Metabolic disorders (e.g., glycogen storage disease type 1b, organic acidurias) |
Fanconi anemia |
Reticular dysgenesis |
Shwachman-Diamond syndrome |
Acquired . |
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Table adapted from: Newburger PE. Neutropenia. In: Rakel RE, Bope ET, eds. Conn’s Current Therapy 2006. Philadelphia: Saunders Elsevier; 2006:502–505 |
Bone marrow aplasia, dysplasia, or replacement |
Drug-induced |
impaired production (chemotherapy, phenothiazines, other drugs) |
antibody-mediated (aminopyrine, other drugs) |
Hypersplenism |
Immune-mediated (alloimmune and autoimmune) |
Nutritional (folate, vitamin B12) |
Sepsis with exhaustion of bone marrow storage pool |
Viral bone marrow suppression |
Congenital |
Cyclic hematopoiesis |
Familial benign neutropenia |
Myelokathexis |
Severe chronic neutropenia |
Complex syndromes including neutropenia |
Cartilage-hair hypoplasia |
Chédiak-Higashi syndrome |
Dyskeratosis congenital |
Primary immunodeficiencies (e.g., X-linked hyper-IgM syndrome) |
Metabolic disorders (e.g., glycogen storage disease type 1b, organic acidurias) |
Fanconi anemia |
Reticular dysgenesis |
Shwachman-Diamond syndrome |