Rituximab alone was effective for the treatment of a diffuse large B-cell lymphoma associated with hemophagocytic syndrome

2007 ◽  
Vol 12 (1) ◽  
pp. 59-62 ◽  
Author(s):  
Takeshi Sano ◽  
Hisashi Sakai ◽  
Kengo Takimoto ◽  
Hitoshi Ohno
2018 ◽  
Vol 46 (1) ◽  
pp. 267-267
Author(s):  
Gautam Phadke ◽  
Dubert Guerrero ◽  
Avish Nagpal ◽  
Hasrat Khan ◽  
Mazen Kherallah ◽  
...  

1996 ◽  
Vol 82 (6) ◽  
pp. 621-624 ◽  
Author(s):  
Gualtiero Büchi ◽  
Giuseppe Termine ◽  
Renzo Orlassino ◽  
Mauro Pagliarino ◽  
Roberto Boero ◽  
...  

A case of splenic large B-cell lymphoma with hemophagocytic syndrome is reported. The difficulties of diagnosis are emphasized especially when peripheral lymph nodes or bone marrow lymphomatous infiltration are not present. Diagnostic criteria for hemophagocytic syndrome and their relationship with the pathogenesis of the disease are also stressed.


2014 ◽  
Vol 60 (04/2014) ◽  
Author(s):  
Xudong Li ◽  
Yi He ◽  
Dongning Wang ◽  
Yuan Hu ◽  
Wenwen Wang ◽  
...  

JRSM Open ◽  
2017 ◽  
Vol 8 (5) ◽  
pp. 205427041769505
Author(s):  
Hisanori Fukunaga ◽  
Kazumasa Kawashima ◽  
Hiromi Kumakawa ◽  
Yuko Hashimoto ◽  
Yuta Takahashi

Intravascular large B-cell lymphoma presents with highly variable symptoms caused by the occlusion of small vessels by neoplastic cells in a variety of organs.


2019 ◽  
Vol 99 (2) ◽  
pp. 381-383
Author(s):  
Shoko Nakayama ◽  
Yasuyoshi Morita ◽  
Jorge Luis Espinoza ◽  
Shinya Rai ◽  
Yasuhiro Taniguchi ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-6
Author(s):  
Yukiko Komeno ◽  
Minako Akiyama ◽  
Yasumi Okochi ◽  
Hitoshi Tokuda ◽  
Keiko Abe ◽  
...  

A 59-year-old man was treated for rheumatoid arthritis (RA) for 12 years with methotrexate (MTX) and prednisolone. After MTX-associated interstitial pneumonia developed, he was treated with cyclophosphamide and prednisolone for 7 months. Arthritis worsened, and tacrolimus was added to the treatment regimen. One month later, he had fever, loss of appetite, and dyspnea on exertion. Blood tests showed pancytopenia with large, atypical lymphocytes. Computed tomography showed mild splenomegaly. Bone marrow examination demonstrated CD20-positive, EBER-positive atypical lymphocytes, and hemophagocytosis. Random skin biopsy led to the diagnosis of intravascular large B-cell lymphoma (IVLBCL). The final diagnosis was a hemophagocytic syndrome-associated variant of IVLBCL. Complete remission was achieved after seven courses of R-CHOP. However, within a month, he complained of dizziness. Magnetic resonance imaging revealed focal infarctions in the cerebellum and around the left lateral ventricle. Central nervous system relapse was suspected. Although salvage chemotherapy (CHASER), whole brain irradiation, and intrathecal injection of cytarabine and prednisolone were temporarily effective, he died. Autopsy revealed infiltration of lymphoma cells in the brain and adrenal glands. To the best of our knowledge, this is the sixth case of IVLBCL and the first case of the hemophagocytic syndrome-associated variant of IVLBCL in RA patients in the literature.


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