Hepatosplenic T cell lymphoma responsive to 2′-deoxycoformycin therapy

被引:15
作者
Bennett, Michael [1 ]
Matutes, Estella [2 ]
Gaulard, Philippe [3 ]
机构
[1] HaEmek Med Ctr, Dept Haematol, IL-18101 Afula, Israel
[2] Royal Marsden Hosp, Dept Haematol, London SW3 6JJ, England
[3] Henri Mondor Hosp, Dept Pathol, Paris, France
关键词
GAMMA-DELTA; CLINICOPATHOLOGICAL ENTITY; HEMOPHAGOCYTIC SYNDROME; ISOCHROMOSOME; 7Q; NK-CELL; FEATURES; ABNORMALITY; EXPRESSION; ORIGIN;
D O I
10.1002/ajh.21774
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatosplenic T cell lymphoma (HSTL) is a rare condition usually with an aggresssive course and a poor prognosis even after extensive treatment. We describe here a patient who presented with hemophagocytosis. The lymphoma had unusual phenotypic features, an indolent course and responded to 2'-deoxycoformycin therapy as a single agent. We suggest that this therapy be used in further cases as part of the treatment strategy.
引用
收藏
页码:727 / 729
页数:3
相关论文
共 18 条
[1]   In vitro and in vivo effects of 2′-deoxycoformycin (Pentostatin) on tumour cells from human γδ+ T-cell malignancies [J].
Aldinucci, D ;
Poletto, D ;
Zagonel, V ;
Rupolo, M ;
Degan, M ;
Nanni, P ;
Gattei, V ;
Pinto, A .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 110 (01) :188-196
[2]   Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic gamma delta T cell lymphoma [J].
Alonsozana, ELC ;
Stamberg, J ;
Kumar, D ;
Jaffe, ES ;
Medeiros, LJ ;
Frantz, C ;
Schiffer, CA ;
OConnell, BA ;
Kerman, S ;
Stass, SA ;
Abruzzo, LV .
LEUKEMIA, 1997, 11 (08) :1367-1372
[3]   Hepatosplenic γδ T-cell lymphoma is a rare clinicopathologic entity with poor outcome:: report on a series of 21 patients [J].
Belhadj, K ;
Reyes, F ;
Farcet, JP ;
Tilly, H ;
Bastard, C ;
Angonin, R ;
Deconinck, E ;
Charlotte, F ;
Leblond, V ;
Labouyrie, E ;
Lederlin, P ;
Emile, JF ;
Delmas-Marsalet, A ;
Arnulf, B ;
Zafrani, ES ;
Gaulard, P .
BLOOD, 2003, 102 (13) :4261-4269
[4]   Hemophagocytic syndrome and hepatosplenic γδ T-cell lymphoma with isochromosome 7q and 8 trisomy [J].
Chin, M ;
Mugishima, H ;
Takamura, M ;
Nagata, T ;
Shichino, H ;
Shimada, T ;
Suzuki, T ;
Harada, K ;
Imashuku, S ;
Yokota, S .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2004, 26 (06) :375-378
[5]  
Cooke CB, 1996, BLOOD, V88, P4265
[6]   Hepatosplenic gamma-delta T-cell lymphoma: clinicopathological features and treatment [J].
Falchook, G. S. ;
Vega, F. ;
Dang, N. H. ;
Samaniego, F. ;
Rodriguez, M. A. ;
Champlin, R. E. ;
Hosing, C. ;
Verstovsek, S. ;
Pro, B. .
ANNALS OF ONCOLOGY, 2009, 20 (06) :1080-1085
[7]  
FARCET JP, 1990, BLOOD, V75, P2213
[8]  
Felgar RE, 1997, AM J PATHOL, V150, P1893
[9]   The serine protease granzyme M is preferentially expressed in NK-cell, γδ T-cell, and intestinal T-cell lymphomas:: evidence of origin from lymphocytes involved in innate immunity [J].
Krenacs, L ;
Smyth, MJ ;
Bagdi, E ;
Krenacs, T ;
Kopper, L ;
Rudiger, T ;
Zettl, A ;
Muller-Hermelink, HK ;
Jaffe, ES ;
Raffeld, M .
BLOOD, 2003, 101 (09) :3590-3593
[10]   Hepatosplenic αβ T-cell lymphomas -: A report of 14 cases and comparison with hepatosplenic γδ T-cell lymphomas [J].
Macon, WR ;
Levy, NB ;
Kurtin, PJ ;
Salhany, KE ;
Elkhalifa, MY ;
Casey, TT ;
Craig, FE ;
Vnencak-Jones, CL ;
Gulley, ML ;
Park, JP ;
Cousar, JB .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (03) :285-296