Two cases of acute myeloid leukemia (AML) presenting with bulky adenopathy are reported. Both patients were febrile at admission and showed massive and diffuse lymph node involvement, hepatomegaly, and splenomegaly. Erythematopapular leukemic skin lesions were present in one case at the onset and developed in the other at the time of relapse. Anemia, thrombocytopenia, and moderate leukocytosis were present in both. The presence of immature cells in peripheral blood and bone marrow allowed a rapid diagnosis of AML, FAB M1, in one patient. In the other case, owing to the paucity of immature cells in peripheral blood and bone marrow, lymph node biopsy with histology, imprint cytology, and immunocytochemistry were essential for the diagnosis (AML, FAB M2, with trilineage dysplasia and basophilic involvement). Both patients achieved complete remission (CR), followed by an early relapse 3 months later. They underwent allogeneic bone marrow transplantation (BMT) from HLA identical siblings. One patient is actually alive and in CR at 6 months after BMT; the other patient showed a leukemic regrowth after transplantation and died 4 months later.

Sica, S., Salutari, P., D'Onofrio, G., Zini Tanzi, G., Laurenti, L., Sora', F., Leone, G., Bulky lymphadenopathy in acute myeloid leukemia, <<ANNALS OF HEMATOLOGY>>, 1998; 77 (1-2): 65-67. [doi:10.1007/s002770050414] [https://hdl.handle.net/10807/343800]

Bulky lymphadenopathy in acute myeloid leukemia

Sica, Simona;Zini Tanzi, Gina;Laurenti, Luca;Sora', Federica;
1998

Abstract

Two cases of acute myeloid leukemia (AML) presenting with bulky adenopathy are reported. Both patients were febrile at admission and showed massive and diffuse lymph node involvement, hepatomegaly, and splenomegaly. Erythematopapular leukemic skin lesions were present in one case at the onset and developed in the other at the time of relapse. Anemia, thrombocytopenia, and moderate leukocytosis were present in both. The presence of immature cells in peripheral blood and bone marrow allowed a rapid diagnosis of AML, FAB M1, in one patient. In the other case, owing to the paucity of immature cells in peripheral blood and bone marrow, lymph node biopsy with histology, imprint cytology, and immunocytochemistry were essential for the diagnosis (AML, FAB M2, with trilineage dysplasia and basophilic involvement). Both patients achieved complete remission (CR), followed by an early relapse 3 months later. They underwent allogeneic bone marrow transplantation (BMT) from HLA identical siblings. One patient is actually alive and in CR at 6 months after BMT; the other patient showed a leukemic regrowth after transplantation and died 4 months later.
1998
Inglese
Sica, S., Salutari, P., D'Onofrio, G., Zini Tanzi, G., Laurenti, L., Sora', F., Leone, G., Bulky lymphadenopathy in acute myeloid leukemia, <<ANNALS OF HEMATOLOGY>>, 1998; 77 (1-2): 65-67. [doi:10.1007/s002770050414] [https://hdl.handle.net/10807/343800]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/343800
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