[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2010, 36(5) 252-254 DOI:     ISSN: 2096-5540 CN: 32-1880/R

����Ŀ¼ | ����Ŀ¼ | ������� | �߼�����                                                            [��ӡ��ҳ]   [�ر�]
����
��չ����
������Ϣ
Supporting info
PDFȫ��
[HTMLȫ��]
�����
�����뷴��
�ѱ����Ƽ�������
�����ҵ����
�������ù�����
����
Email Alert
���·���
���������Ϣ
���Ĺؼ����������
�������ަ��
��ʽϸ����
S��zary�ۺ���
�ܰ�����Tϸ����Ƥ��
���������������
��Ծƽ
������
PubMed
Article by Zeng,T.B
Article by Yu,B.X

��ʽϸ������ަ����ѿ�׺�S��zary�ۺ����е�Ӧ��

��Ծƽ1,������2

1. ����Э��ҽԺƤ����
2. �й�ҽѧ��ѧԺƤ�����о���

ժҪ��

��ʽϸ���Ǿ��п��١�������ͬʱ��������ϸ�����Ե����ƣ���Խ��Խ�㷺Ӧ����Ƥ��Tϸ���ܰ�������ʽϸ���ǿ�ͨ��Tϸ�����濹ԭ��Ӧ�����Tϸ������V�¿���ֱ���������Tϸ�����쳣���߱��ͼ�����¡�ԣ���Ϊަ����ѿ�׺�S��zary�ۺ���������Ϻ����Ƽ�����Ҫ���ߣ����ڰ�����Ѫ���۵�ަ����ѿ�׺�S��zary�ۺ�����Ϻ����Ƽ���������������о��е�Ӧ�ý����и��ӹ�����ǰ����

�ؼ����� �������ަ��   ��ʽϸ����   S��zary�ۺ���   �ܰ�����Tϸ����Ƥ��  

Application of flow cytometry in mycosis fungoides and S��zary syndrome

Abstract:

Flow cytometry ��FCM�� has been more and more widely applied in the researches of cutaneous T-cell lymphoma for its capability to rapidly and simultaneously analyze properties of multiple cells in a quantitative manner. Since FCM could detect abnormal immunophenotypes and monoclonality of neoplastic T cells using antibodies to T-cell superficial antigens and T-cell receptor beta-chain variable region families ��TCR-V �£�, respectively, it has become an important tool for ancillary diagnosis and monitoring of therapeutic response, of mycosis fungoides and S��zary syndrome with peripheral blood involvement.

Keywords: flow cytometry   S��zary syndrome  
�ո����� 2010-02-03 �޻����� 2010-04-26 ����淢������ 2010-09-15 
DOI:
������Ŀ:

ͨѶ����: ��Ծƽ
���߼��:

�ο����ף�
[1] Hwang ST, Janik JE, Jaffe ES, et al. Mycosis fungoides and Sezary syndrome. Lancet, 2008,371(9616):945-957. [2] Willemze R, Jaffe ES, Burg G, et al. WHO-EORTC classification for cutaneous lymphomas. Blood, 2005,105(10):3768-3785. [3] Oshtory S, Apisarnthanarax N, Gilliam AC, et al. Usefulness of flow cytometry in the diagnosis of mycosis fungoides. J Am Acad Dermatol, 2007,57(3):454-462. [4] Feng B, Jorgensen JL, Jones D, et al. Flow cytometric detection of peripheral blood involvement by mycosis fungoides and Sezary syndrome using T-cell receptor Vbeta chain antibodies and its application in blood staging. Mod Pathol, 2009. [5] Bergman R. How useful are T-cell receptor gene rearrangement studies as an adjunct to the histopathologic diagnosis of mycosis fungoides? Am J Dermatopathol, 1999,21(5):498-502. [6] Chen M, Deng A, Crowson AN, et al. Assessment of T-cell clonality via T-cell receptor-gamma rearrangements in cutaneous T-cell-dominant infiltrates using polymerase chain reaction and single-stranded DNA conformational polymorphism assay. Appl Immunohistochem Mol Morphol, 2004,12(4):373-379. [7] ����ϼ. ��ʽϸ�����������ٴ����о��е�Ӧ��. �й�ҽѧ������־, 2008,9(1):42��47. [8] Stetler-Stevenson M. Flow cytometry in lymphoma diagnosis and prognosis: useful? Best Pract Res Clin Haematol, 2003,16(4):583-597. [9] Vonderheid EC, Bernengo MG, Burg G, et al. Update on erythrodermic cutaneous T-cell lymphoma: report of the International Society for Cutaneous Lymphomas. J Am Acad Dermatol, 2002,46(1):95-106. [10] Harmon CB, Witzig TE, Katzmann JA, et al. Detection of circulating T cells with CD4+CD7- immunophenotype in patients with benign and malignant lymphoproliferative dermatoses. J Am Acad Dermatol, 1996,35(3 Pt 1):404-410. [11] Bernengo MG, Novelli M, Quaglino P, et al. The relevance of the CD4+ CD26- subset in the identification of circulating Sezary cells. Br J Dermatol, 2001,144(1):125-135. [12] Laetsch B, Haffner AC, Dobbeling U, et al. CD4 + /CD7- T cell frequency and polymerase chain reaction-based clonality assay correlate with stage in cutaneous T cell lymphomas. J Invest Dermatol, 2000,114(1):107-111. [13] Sokolowska-Wojdylo M, Wenzel J, Gaffal E, et al. Absence of CD26 expression on skin-homing CLA+ CD4+ T lymphocytes in peripheral blood is a highly sensitive marker for early diagnosis and therapeutic monitoring of patients with Sezary syndrome. Clin Exp Dermatol, 2005,30(6):702-706. [14] Vonderheid EC. On the diagnosis of erythrodermic cutaneous T-cell lymphoma. J Cutan Pathol, 2006,33 Suppl 1:27-42. [15] Kelemen K, Guitart J, Kuzel TM, et al. The usefulness of CD26 in flow cytometric analysis of peripheral blood in Sezary syndrome. Am J Clin Pathol, 2008,129(1):146-156. [16] Fierro MT, Novelli M, Quaglino P, et al. Heterogeneity of circulating CD4+ memory T-cell subsets in erythrodermic patients: CD27 analysis can help to distinguish cutaneous T-cell lymphomas from inflammatory erythroderma. Dermatology, 2008,216(3):213-221. [17] Edelman J, Meyerson HJ. Diminished CD3 expression is useful for detecting and enumerating Sezary cells. Am J Clin Pathol, 2000,114(3):467-477. [18] Morice WG, Kimlinger T, Katzmann JA, et al. Flow cytometric assessment of TCR-Vbeta expression in the evaluation of peripheral blood involvement by T-cell lymphoproliferative disorders: a comparison with conventional T-cell immunophenotyping and molecular genetic techniques. Am J Clin Pathol, 2004,121(3):373-383. [19] Morice WG, Katzmann JA, Pittelkow MR, et al. A comparison of morphologic features, flow cytometry, TCR-Vbeta analysis, and TCR-PCR in qualitative and quantitative assessment of peripheral blood involvement by Sezary syndrome. Am J Clin Pathol, 2006,125(3):364-374. [20] Washington LT, Huh YO, Powers LC, et al. A stable aberrant immunophenotype characterizes nearly all cases of cutaneous T-cell lymphoma in blood and can be used to monitor response to therapy. BMC Clin Pathol, 2002,2(1):5. [21] Introcaso CE, Micaily B, Richardson SK, et al. Total skin electron beam therapy may be associated with improvement of peripheral blood disease in Sezary syndrome. J Am Acad Dermatol, 2008,58(4):592-595. [22] Schwab C, Willers J, Niederer E, et al. The use of anti-T-cell receptor-Vbeta antibodies for the estimation of treatment success and phenotypic characterization of clonal T-cell populations in cutaneous T-cell lymphomas. Br J Haematol, 2002,118(4):1019-1026. [23] Ferenczi K, Yawalkar N, Jones D, et al. Monitoring the decrease of circulating malignant T cells in cutaneous T-cell lymphoma during photopheresis and interferon therapy. Arch Dermatol, 2003,139(7):909-913
�������������

�������� (��ע��:��վʵ�������Ը�, �벻Ҫ������ѧ���޹ص�����!�������ݲ�����վ�۵�.)

Copyright 2008 by ����Ƥ���Բ�ѧ��־