N. Ichikawa et al., AGGRESSIVE GRANULAR LYMPHOCYTE LEUKEMIA OF NATURAL-KILLER-CELL TYPE IN AN ELDERLY PATIENT, Internal medicine, 32(11), 1993, pp. 882-885
A 75-year-old man was admitted to our hospital because of intermittent
fever. His peripheral blood picture showed granular lymphocyte (GL) p
roliferation. The GLs were immunologically and functionally phenotyped
as natural killer cells. Chromosomal analysis of peripheral lymphocyt
es with interleukin-2 stimulation revealed an inversion of chromosome
9 with an unusual breakpoint, showing abnormal monoclonal proliferatio
n of the GLs. Progressive increase of GL count and hepatosplenomegaly
necessitated the start of combined chemotherapy. His condition was com
plicated by icterus and renal failure, and he died finally of respirat
ory failure. Autopsy revealed disseminated intravascular coagulation a
nd infiltration of GLs in the bone marrow, spleen, and liver.