Poly(A)-Polymerase Activity in Chronic Lymphocytic Leukemia of the B Cell Type

1985 ◽  
Vol 74 (1) ◽  
pp. 31-34 ◽  
Author(s):  
Gerassimos A. Pangalis ◽  
Theoni Trangas ◽  
Constantinos J. Papanastasiou ◽  
Paraskevi A. Roussou ◽  
Milton Tsiapaîis
2005 ◽  
Vol 10 (5) ◽  
pp. 357-361 ◽  
Author(s):  
Naoko Watanabe ◽  
Takayuki Takahashi ◽  
Naoshi Sugimoto ◽  
Yasuhiro Tanaka ◽  
Masayuki Kurata ◽  
...  

1988 ◽  
Vol 6 (1) ◽  
pp. 47-55 ◽  
Author(s):  
E. Kimby ◽  
H. Mellstedt ◽  
B. Nilsson ◽  
M. Björkholm ◽  
G. Holm ◽  
...  

Blood ◽  
1983 ◽  
Vol 62 (6) ◽  
pp. 1176-1181 ◽  
Author(s):  
K Sheibani ◽  
SJ Forman ◽  
CD Winberg ◽  
H Rappaport

Abstract Although rare cases of chronic lymphocytic leukemia (CLL) of the T-cell type have been reported, CLL is more commonly found to be a neoplastic lymphoproliferative disease of B-cell origin. In this article, we describe a patient with long-standing CLL that was immunologically shown to be of the B-cell type, who, during the course of his disease, developed cutaneous T-cell lymphoma (CTCL), which was shown to be of the helper/inducer subtype. The neoplastic lymphoid cells in the skin infiltrate differed morphologically and immunologically from those in the peripheral blood. The occurrence of CTCL during this patient's clinical course represents a second neoplasm arising from a different cell line, rather than a tissue manifestation of the patient's CLL. To our knowledge, this is the first report in which the occurrence of CTCL is documented in a patient with immunologically known B-cell CLL. In addition to establishing the presence of B-cell CLL and CTCL of the helper/inducer T-cell type in the same patient, this case report demonstrates the usefulness and necessity of evaluating lymphoproliferative disorders by means of a multidisciplinary approach.


Blood ◽  
1983 ◽  
Vol 62 (6) ◽  
pp. 1176-1181
Author(s):  
K Sheibani ◽  
SJ Forman ◽  
CD Winberg ◽  
H Rappaport

Although rare cases of chronic lymphocytic leukemia (CLL) of the T-cell type have been reported, CLL is more commonly found to be a neoplastic lymphoproliferative disease of B-cell origin. In this article, we describe a patient with long-standing CLL that was immunologically shown to be of the B-cell type, who, during the course of his disease, developed cutaneous T-cell lymphoma (CTCL), which was shown to be of the helper/inducer subtype. The neoplastic lymphoid cells in the skin infiltrate differed morphologically and immunologically from those in the peripheral blood. The occurrence of CTCL during this patient's clinical course represents a second neoplasm arising from a different cell line, rather than a tissue manifestation of the patient's CLL. To our knowledge, this is the first report in which the occurrence of CTCL is documented in a patient with immunologically known B-cell CLL. In addition to establishing the presence of B-cell CLL and CTCL of the helper/inducer T-cell type in the same patient, this case report demonstrates the usefulness and necessity of evaluating lymphoproliferative disorders by means of a multidisciplinary approach.


2006 ◽  
Vol 12 (4) ◽  
pp. 187-192
Author(s):  
F. Scamardella ◽  
M. Maconi ◽  
L. Albertazzi ◽  
B. Gamberi ◽  
L. Gugliotta ◽  
...  

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