Acquired adult red cell aplasia due to thymoma
Acquired adult red cell aplasia with thymoma
Acquired pure red cell aplasia
Pure red cell aplasia, acquired
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia and selective erythroid hypoplasia. It can occur as a chronic or acute form; the former is predominantly seen in adults and the latter in children. Pathogenesis involves immune dysfunction with antibodies directed against erythroid precursor cells or erythropoietin, or due to t-cell mediated suppression of erythropoiesis.
A rare disorder in which the bone marrow makes almost no red blood cells. It may be caused by infection or by certain drugs. Patients with this disorder may also have a thymoma a tumor of the thymus) or an autoimmune condition such as lupus erythematosus or rheumatoid arthritis.
D60.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM D60.9 became effective on October 1, 2022.
This is the American ICD-10-CM version of D60.9 – other international versions of ICD-10 D60.9 may differ.