Immunophenotypes and Gene Rearrangements of the T-Cell Receptor in Two Patients with a Large Granular Lymphocyte Disorder.

Abstract:

:Large granular lymphocyte disorder (LGLD) is a lymphoproliferative disease, characterized by moderate lymphocytosis with an excess of large granular lymphocytes, neutropenia, anemia, and a variable, but mostly chronic clinical course. We describe two patients with LGLD. One patient presented with symptomatic corticoster-oid-responsive hemolytic anemia, while the other had a chronic course not requiring therapy. The majority of lymphocytes from both patients were CD8 + T lymphocytes. However, the cells from the two patients differed in the molecular pattern of the T cell receptor (TCR), and this may explain the difference in their clinical course.

journal_name

Leuk Lymphoma

journal_title

Leukemia & lymphoma

authors

Peller S,Kaufman S,Rotter V

doi

10.3109/10428199109064883

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

83-7

issue

1

eissn

1042-8194

issn

1029-2403

journal_volume

6

pub_type

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