scholarly journals S2734 Sinusoidal Obstruction Syndrome in a Leukemia Patient Treated With Inotuzumab

2021 ◽  
Vol 116 (1) ◽  
pp. S1143-S1143
Author(s):  
Shaleen Vasavada ◽  
Hao Chi Zhang
2010 ◽  
Vol 76 (3) ◽  
pp. 250-251 ◽  
Author(s):  
L.-X. Yan ◽  
F.-M. Zhu ◽  
W. Wang ◽  
W. Zhang ◽  
H.-J. Lv

Author(s):  
Margarete Voigt ◽  
Konrad Sinn ◽  
Amer Malouhi ◽  
Thomas Gecks ◽  
Jan Zinke ◽  
...  

Author(s):  
Thomas Luft ◽  
Peter Dreger ◽  
Aleksandar Radujkovic

AbstractAllogeneic hematopoietic stem cell transplantation (alloSCT) carries the promise of cure for many malignant and non-malignant diseases of the lympho-hematopoietic system. Although outcome has improved considerably since the pioneering Seattle achievements more than 5 decades ago, non-relapse mortality (NRM) remains a major burden of alloSCT. There is increasing evidence that endothelial dysfunction is involved in many of the life-threatening complications of alloSCT, such as sinusoidal obstruction syndrome/venoocclusive disease, transplant-associated thrombotic microangiopathy, and refractory acute graft-versus host disease. This review delineates the role of the endothelium in severe complications after alloSCT and describes the current status of search for biomarkers predicting endothelial complications, including markers of endothelial vulnerability and markers of endothelial injury. Finally, implications of our current understanding of transplant-associated endothelial pathology for prevention and management of complications after alloSCT are discussed.


Blood ◽  
1989 ◽  
Vol 73 (3) ◽  
pp. 814-817 ◽  
Author(s):  
B Opalka ◽  
U Wandl ◽  
O Kloke ◽  
C Oberle ◽  
J Koppe ◽  
...  

Abstract The BCR gene on chromosome 22 has received increasing attention because of its involvement in the Philadelphia (Ph′) translocation. For most restriction enzymes, this locus has been found to be nonpolymorphic. Two alleles have only been found when Taql-digested DNA is hybridized to a 5′ bcr-specific probe. We describe another two-allele polymorphism detected by the same probe in PvuII-digested DNA. The polymorphism is characterized by an additional PvuII site in the bcr region: this causes the appearance of an additional band of about 2.3 kb or 2.5 kb besides a 4.8-kb fragment in hybridizations with the 5′ bcr or a 3′ bcr probe. The incidence of the second allele is very low. It has only been found in some patients with hematopoietic malignancies and in a group of volunteers having a leukemia patient in their families.


2007 ◽  
Vol 48 (12) ◽  
pp. 2461-2464 ◽  
Author(s):  
Ricardo García-Muñoz ◽  
Alicia Galar ◽  
Cristina Moreno ◽  
Paula Rodríguez-Otero ◽  
Elena Panizo-Morgado ◽  
...  

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