Abstract
Leukemia cutis (LC) is the infiltration of skin by malignant cells in the context of leukemia. Acute myelogenous leukemia (AML) is associated with leukemia cutis in approximately 4 % of cases overall, but certain subtypes have higher rates of LC. Acute myelomonocytic leukemia (FAB classification) represented the majority (56 %) in one large case series. Abnormalities of chromosome 8 on molecular studies were more common in patients with AML and leukemia cutis (36 %) than in patients with AML without leukemia cutis (2.8 %). In cases which have associated coagulopathy, hemorrhagic lesions may be present. Leukemia cutis prior to bone marrow involvement in AML is exceptional (0.01 % of total cases, 0.1 % of leukemia cutis cases). Relapse of skin disease prior to bone marrow involvement is more common but is still quite rare. In a large series of AML patients, additional extramedullary leukemic spread, particularly meningeal disease, were present in 90 % and 33 % of patients with leukemia cutis, respectively. “Congenital” leukemia refers to that which presents within 1 month of birth and is usually of myeloid lineage, usually FAB class M4 or M5. Leukemia cutis in congenital leukemia occurs in 25–30 % of affected infants, often in those with high tumor burden and hepatosplenomegaly.
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Crowe, D.R. (2016). Leukemia Cutis. In: Crowe, D., Morgan, M., Somach, S., Trapp, K. (eds) Deadly Dermatologic Diseases. Springer, Cham. https://doi.org/10.1007/978-3-319-31566-9_4
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DOI: https://doi.org/10.1007/978-3-319-31566-9_4
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