Intravascular large B-cell lymphoma presenting with mass lesions in the central nervous system: A report of five cases

被引:36
作者
Imai, H
Kajimoto, K
Taniwaki, M
Miura, I
Hatta, Y
Hashizume, Y
Watanabe, M
Shiraishi, T
Nakamura, S
机构
[1] Mie Univ, Sch Med, Dept Pathol, Tsu, Mie 5148507, Japan
[2] Aichi Canc Ctr Hosp, Dept Pathol, Nagoya, Aichi 464, Japan
[3] Aichi Canc Ctr Hosp, Clin Labs, Nagoya, Aichi 464, Japan
[4] Kyoto Prefectural Univ Med, Dept Internal Med 3, Kyoto 602, Japan
[5] Akita Univ, Sch Med, Dept Internal Med 3, Akita 010, Japan
[6] Nihon Univ, Sch Med, Dept Internal Med 1, Tokyo, Japan
[7] Aichi Med Univ, Inst Med Sci Aging, Nagoya, Aichi, Japan
关键词
B-cell; biopsy; brain; diagnosis; intravascular; lymphoma;
D O I
10.1111/j.1440-1827.2004.01613.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We have encountered five cases of intravascular large B-cell lymphoma (IVL) presenting with central nervous system (CNS) mass lesions during their clinical course. The age of the patients ranged from 50 to 74 years and three patients were male. All of these cases histopathologically showed typical intravascular localization of the neoplastic cells in the initial biopsy specimens obtained from sites other than the CNS. Despite multiagent chemotherapy, patients suffered from single or multiple CNS mass lesions 5-44 months after the initial diagnosis of IVL, except for one case in which IVL and the CNS mass lesion were diagnosed at the same time. The subsequent biopsy and autopsy specimens obtained from the CNS mass lesions revealed diffuse infiltration of the tumor cells with perivascular spreading, but minimal or no intravascular components. Immunohistochemical analysis of intravascular tumor cells and CNS mass lesions revealed expression of CD20, CD79a, bcl-2 and negative for CD3e and Epstein-Barr virus encoded RNA. The overall features of the CNS mass lesions were very similar to or indistinguishable from those of the primary CNS lymphomas. This implies that CNS mass lesions in the IVL cases can be correctly diagnosed only by careful attention to clinical and pathological findings. Moreover, there is the possibility that some cases previously diagnosed as primary CNS lymphomas may have include IVL cases. Further investigation is needed to explore this unusual phenomenon.
引用
收藏
页码:231 / 236
页数:6
相关论文
共 31 条
[11]  
2-O
[12]  
HENRY JM, 1974, CANCER, V34, P1293, DOI 10.1002/1097-0142(197410)34:4<1293::AID-CNCR2820340441>3.0.CO
[13]  
2-P
[14]  
Jaffe ES., 2001, WHO CLASSIFICATION T
[15]   LYMPHOCYTE HOMING RECEPTORS AND ADHESION MOLECULES IN INTRAVASCULAR MALIGNANT LYMPHOMATOSIS [J].
JALKANEN, S ;
AHO, R ;
KALLAJOKI, M ;
EKFORS, T ;
NORTAMO, P ;
GAHMBERG, C ;
DUIJVESTIJN, A ;
KALIMO, H .
INTERNATIONAL JOURNAL OF CANCER, 1989, 44 (05) :777-782
[16]  
KAYANO H, 1990, ARCH PATHOL LAB MED, V114, P580
[17]  
Khalidi HS, 1998, MODERN PATHOL, V11, P983
[18]   Multicolor karyotyping and clinicopathological analysis of three intravascular lymphoma cases [J].
Khoury, H ;
Lestou, VS ;
Gascoyne, RD ;
Bruyere, H ;
Li, CH ;
Nantel, SH ;
Dalal, BI ;
Naiman, SC ;
Horsman, DE .
MODERN PATHOLOGY, 2003, 16 (07) :716-724
[19]   Heterogeneity of endothelial cells from different organ sites in T-cell subset recruitment [J].
Lim, YC ;
Garcia-Cardena, G ;
Allport, JR ;
Zervoglos, M ;
Connolly, AJ ;
Gimbrone, MA ;
Luscinskas, FW .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (05) :1591-1601
[20]   Intravascular lymphomatosis (IL) in a child mimicking a posterior fossa tumor [J].
Massimino, M ;
Giardini, R ;
Cefalo, G ;
Simonetti, F ;
Pollo, B ;
Giombini, S ;
Tesoro-Tess, JD ;
Ponzoni, M ;
Patriarca, C .
JOURNAL OF NEURO-ONCOLOGY, 2001, 51 (01) :47-50