Journal List > Korean J Hematol > v.41(2) > 1032662

Lee, Choi, Lee, Lee, Park, Choi, Lee, and Kim: Tumor Lysis Syndrome in Lymphoblastic Crisis of CML

Abstract

Tumor lysis syndrome (TLS) defines the metabolic derangements that occur with tumor breakdown following the initiation of cytotoxic therapy. TLS results from the rapid destruction of malignant cells and the abrupt release of intracellular materials and their metabolites into the extracellular space. The syndrome causes hyperuricemia, hyperkalemia, hyperphosphatemia, secondary hypocalcemia and uremia. It can result in acute renal failure and be fatal. Early recognition of patient at risk and preventive measures are important. There is a high incidence of TLS in tumors with high proliferative rates and large burden such as acute lymphoblastic leukemia and Burkitt's lymphoma. It less commonly occurs in solid tumors such as testicular cancer, breast cancer and small cell lung cancer. There are only a few reports on TLS complicated in CML in blast crisis. So we report a 45-yr-old woman presenting with TLS associated with CML in lymphoblastic crisis after the initiation of cytotoxic chemotherapy.

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Fig. 1
Peripheral blood smear. Marked leukocytosis composed of immature blasts (44%), band form (5%), promyelocyte (3%), myelocyte (10%), metamyelocyte (7%), segmented neutrophils (13%), eosinophils (3%), monocyte (2%) and lymphocytes (9%) is observed. Moderate decrease of platelet component is also observed. (A) ×40, (B) ×200.
kjh-41-119f1.tif
Fig. 2
Bone marrow biopsy. (A) Bone marrow biopsy imprint (touch preparation), More than 30% of all hematopoietic cells are replaced by immature cells. These cells show high nuclear/ cytoplasmic ratio, one or more prominent nucleoli, and fine nuclear chromatin. These cells also vary in size from medium to large. The myeloid series are increased in proportion and reveal normal maturation. The erythroid series are decreased in proportion and reveal normal maturation. The megakaryocytes are decreased in number. (B) The bone marrow section is hypercellular (90%) for her age. Immature cells are seen throughout section intermingled with other hematopoietic cells.
kjh-41-119f2.tif
Table 1.
Immunophenotyping result
Anti Anti Anti Anti Anti Anti Anti Anti Anti Anti Anti Anti
CD3 CD5 CD7 CD10 CD13 CD14 CD19 CD20 CD22 CD33 CD34 CD45
(-) (-) (-) (+) (+)∗ (-) (+) (-) (+) (-) (+) (+)

∗CD13: abberant expression. CD10: 80.38%, CD13: 58.05%, CD19: 77.94%, CD22: 68.66%, CD34: 85.32%, CD45: 93.64%.

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