A unique pattern of central nervous system leukemia in acute myelomonocytic leukemia associated with inv(16)(p13q22).

A unique pattern of central nervous system leukemia in acute myelomonocytic leukemia associated with inv(16)(p13q22).
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与 inv(16)(p13q22) 相关的急性粒单核细胞白血病中枢神经系统白血病的独特模式。

DOI:
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发表时间:
1985
期刊:
影响因子:
20.3
通讯作者:
E. Freireich
E. Freireich
中科院分区:
医学1区
文献类型:
--
作者:
R. Holmes;M. Keating;A. Cork;Y. Broach;J. Trujillo;W. Dalton;K. McCredie;E. Freireich

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Twenty-six patients with inv(16)(p13q22) or del(16)(q22) in association with acute myelomonocytic leukemia (AMML-M4, FAB classification), and abnormal marrow eosinophils have been treated at this institute. Initial bone marrow eosinophilia (greater than or equal to 4%) was observed in 22 of 26 patients (85%), and abnormal eosinophil morphology, characterized by immature cells with some interspersed basophilic granules, was evident in 26 of 26 (100%). Giemsa-banded chromosome analysis performed in all patients revealed 16 cases with inv(16)(p13q22) alone, and ten cases with additional chromosome changes. Twenty-five patients received combination induction chemotherapy, and 23 (92%) achieved complete remission (CR). The median duration of remission was 18 months (range, six to 72 + months), and the median duration of survival was 34 months (range, 0.5 to 133 months). Nine patients (35%) relapsed in the CNS at a median time of 19 months (range, six to 133 months) from first marrow CR. All patients had leptomeningeal disease, and in addition, six of nine (66%) demonstrated two or more enhancing lesions on computed tomography brain scan, consistent with intracerebral myeloblastomas. Review of 384 Giemsa-banded patients with acute myeloid leukemia revealed no other morphologic or cytogenetic subgroup with either an equivalent incidence of CNS leukemia or documented intracerebral myeloblastomas. This series of inv(16)(p13q22)/del(16)(q22) AMML reports a favorable prognosis for such patients and associates a specific clonal cytogenetic subgroup of acute leukemia with a distinct propensity for CNS relapse, manifesting as leptomeningeal disease and intracerebral myeloblastomas.
DOI: 10.1056/nejm198309153091103
发表时间: 1983-01-01
影响因子: 158.5
作者:
LEBEAU, MM;LARSON, RA;ROWLEY, JD
通讯作者: ROWLEY, JD
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发表时间: 1981-07
期刊: The New England journal of medicine
影响因子: --
作者:
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通讯作者: J. Yunis;C. Bloomfield;K. Ensrud
DOI: --
发表时间: 1984
影响因子: --
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DOI: 10.1016/s0147-0272(83)80005-1
发表时间: 1983
影响因子: 2.6
作者:
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通讯作者: Poste,G
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发表时间: 1981-01-01
影响因子: 15.9
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