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Large granular lymphocytic leukemia: molecular pathogenesis, clinical manifestations, and treatment.大颗粒淋巴细胞白血病:分子发病机制、临床表现和治疗。
Hematology Am Soc Hematol Educ Program. 2012;2012:652-9. doi: 10.1182/asheducation-2012.1.652.
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T-cell large granular leukemia and related proliferations.T细胞大颗粒淋巴细胞白血病及相关增殖性疾病。
Am J Clin Pathol. 2007 Jun;127(6):850-9. doi: 10.1309/A8FHDA0VVRJ05GJP.
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Aggressive T-cell large granular lymphocyte leukemia: a case report and review of the literature.侵袭性T细胞大颗粒淋巴细胞白血病:一例报告并文献复习
Am J Hematol. 2007 Jun;82(6):481-5. doi: 10.1002/ajh.20853.
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T-cell large granular lymphocyte leukemias have multiple phenotypic abnormalities involving pan-T-cell antigens and receptors for MHC molecules.T细胞大颗粒淋巴细胞白血病有多种表型异常,涉及全T细胞抗原和MHC分子受体。
Am J Clin Pathol. 2005 Dec;124(6):937-46.
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T-cell large granular lymphocyte leukemia and related disorders.T细胞大颗粒淋巴细胞白血病及相关疾病
Oncologist. 2004;9(3):247-58. doi: 10.1634/theoncologist.9-3-247.
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Distinct bone marrow findings in T-cell granular lymphocytic leukemia revealed by paraffin section immunoperoxidase stains for CD8, TIA-1, and granzyme B.通过针对CD8、TIA-1和颗粒酶B的石蜡切片免疫过氧化物酶染色揭示的T细胞颗粒淋巴细胞白血病中独特的骨髓表现。
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Aggressive variant of morphologically typical T large granular lymphocyte leukemia/lymphoma lacking NK cell markers.
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8
Hepatosplenic T cell lymphoma. A review on 45 cases since the first report describing the disease as a distinct lymphoma entity in 1990.肝脾T细胞淋巴瘤。自1990年首次将该疾病描述为一种独特的淋巴瘤实体以来的45例病例综述。
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Clinicopathological features of aggressive large granular lymphocyte leukaemia resemble Fas ligand transgenic mice.
Br J Haematol. 2000 Mar;108(4):717-23. doi: 10.1046/j.1365-2141.2000.01934.x.
10
Aggressive acute CD3+, CD56- T cell large granular lymphocyte leukemia with two stages of maturation arrest.侵袭性急性CD3+、CD56- T细胞大颗粒淋巴细胞白血病伴两个成熟停滞阶段。
Leukemia. 1996 Sep;10(9):1514-9.

CD56阴性侵袭性T细胞大颗粒淋巴细胞白血病

CD56 Negative Aggressive T Cell Large Granular Lymphocytic Leukemia.

作者信息

Sylvia Mary Theresa, Jacob Sajini Elizabeth, Basu Debdatta, Amalnath Deepak, Dutta Tarun Kumar

机构信息

Department of Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Gorimedu, Puducherry, 605011 Puducherry India.

Department of Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Gorimedu, Puducherry, 605011 Puducherry India.

出版信息

Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):121-4. doi: 10.1007/s12288-015-0502-9. Epub 2015 Jan 13.

DOI:10.1007/s12288-015-0502-9
PMID:27408372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4925484/
Abstract

T cell large granular lymphocytic leukemia is a clonal proliferation of cytotoxic large granular T cells positive for CD3 and CD8. It is a chronic lymphoproliferative disorder with an indolent course. Therapeutic options include observation and low dose chemotherapy. Rarely, they have an aggressive course. Such cases have expression of NK cell associated antigens like CD56 in the T cells. These cases require more aggressive therapy with acute lymphoblastic leukemia regimens. We report a case of fatal CD56 negative T cell large granular lymphocytic leukemia in a 38 year old lady.

摘要

T细胞大颗粒淋巴细胞白血病是一种细胞毒性大颗粒T细胞的克隆性增殖,这些T细胞CD3和CD8呈阳性。它是一种病程缓慢的慢性淋巴细胞增殖性疾病。治疗选择包括观察和低剂量化疗。极少数情况下,其病程呈侵袭性。此类病例中T细胞表达NK细胞相关抗原,如CD56。这些病例需要采用急性淋巴细胞白血病治疗方案进行更积极的治疗。我们报告一例38岁女性致命性CD56阴性T细胞大颗粒淋巴细胞白血病病例。