Chronic granulocytic leukaemia presenting with an extramedullary T lymphoblastic crisis.

Abstract:

:A 33-year-old man presented with hepatosplenomegaly and lymphadenopathy. Bone marrow findings were consistent with Philadelphia-positive accelerated-phase chronic granulocytic leukaemia (CGL). Lymph node histology and immunhistochemistry were diagnostic of T lymphoblastic lymphoma. Molecular studies on lymph node DNA identified rearrangement within the major breakpoint cluster region (M-bcr), indicating a common clonal origin of CGL and the T lymphoblastic lymphoma. We report the second case where extramedullary T lymphoblastic crisis was the presenting feature of CGL.

journal_name

Br J Haematol

authors

Jacob A,Rowlands DC,Patton N,Holmes JA

doi

10.1111/j.1365-2141.1994.tb05050.x

subject

Has Abstract

pub_date

1994-10-01 00:00:00

pages

435-6

issue

2

eissn

0007-1048

issn

1365-2141

journal_volume

88

pub_type

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