Cytogenetic evidence of metastatic myxoid liposarcoma and therapy-related myelodysplastic syndrome in a bone marrow biopsy

被引:2
作者
Rossi, Sabrina [1 ]
Canal, Fabio [1 ]
Licci, Stefano [2 ]
Zanatta, Lucia [1 ]
Laurino, Licia [1 ]
Gottardi, Michele [3 ]
Gherlinzoni, Filippo [3 ]
Tos, Angelo Paolo Dei [1 ]
机构
[1] Gen Hosp, Dept Pathol, I-31100 Treviso, Italy
[2] Santo Spirito Hosp, Dept Pathol, I-60184 Rome, Italy
[3] Gen Hosp, Dept Hematol, I-31100 Treviso, Italy
关键词
Myxoid liposarcoma; Bone metastasis; Therapy-related myelodysplastic syndrome; RAEB; cytogenetics; FISH; MYELOID-LEUKEMIA; TLS-CHOP; GENE; ECTEINASCIDIN-743; LEUKEMOGENESIS; CHEMOTHERAPY; SARCOMA; MLL;
D O I
10.1016/j.humpath.2008.12.020
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Myxoid liposarcoma exhibits a peculiar clinical behavior, with a tendency to spread to serosal membranes, distant soft tissues, and bones, even in the absence of lung metastases. Therapy-related hematological neoplasms are well-known side effects of cytotoxic chemotherapy. We describe an exceptional case of metastatic myxoid liposarcoma of the spine associated with therapy-related refractory anemia with excess of blasts in a 37-year-old woman who underwent multi-agent chemotherapy for a myxoid liposarcoma of the left thigh. Microscopic examination of the bone marrow biopsy revealed dysplastic features, with abnormal localization of immature precursors and micromegakaryocytes, and islands of undifferentiated oval small/medium-size cells, suggestive of acute myeloid leukemia arising in the setting of a myelodysplastic syndrome. Immunohistochemistry was not discriminant. Cytogenetic analyses of bone marrow aspirate disclosed the presence of 2 different rearrangements, subsequently confirmed by fluorescent in situ hybridization and was crucial in making the correct diagnosis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1040 / 1044
页数:5
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