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Clinical and laboratory investigation of hematological malignancy patients carrying 3q21q26 rearrangement / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 696-698, 2007.
Article in Chinese | WPRIM | ID: wpr-229841
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the clinical and laboratory characteristics of various hematopoietic malignant patients with t(3;3)(q21;q26) or inv(3) (q21q26).</p><p><b>METHODS</b>Bone marrow samples were collected at presentation, prepared by short-time unstimulated culture and R-binding, and karyotyped by conventional cytogenetical assay (CCA); megalokaryocytes were detected by Streptavidin-AKP (SAP); immunotype of the leukemia cells was tested by flow cytometric anylysis of surface antigens (FACS).</p><p><b>RESULTS</b>All of the 9 hematopoietic malignant patients with t(3;3)(q21;q26) or inv(3) (q21q26) manifested myelodysplasia and poor treatment response. One of them relapsed shortly after allogenic hemotopoietic stem cell transplantation (allo-HSCT).</p><p><b>CONCLUSION</b>Patients with 3q21q26 rearrangement can be found in various hematopoietic malignances and demonstrate an unique entity. These patients show poor treatment response and have extremely poor prognosis.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Translocation, Genetic / Myelodysplastic Syndromes / Chromosomes, Human, Pair 3 / Gene Rearrangement / Leukemia / Chromosome Mapping / Hematologic Neoplasms / Genetics / Chromosome Inversion Type of study: Prognostic study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Translocation, Genetic / Myelodysplastic Syndromes / Chromosomes, Human, Pair 3 / Gene Rearrangement / Leukemia / Chromosome Mapping / Hematologic Neoplasms / Genetics / Chromosome Inversion Type of study: Prognostic study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2007 Type: Article