Reprinted from the Journal of the American Medical Association
June 30, 1975 Volume 232
Copyright 1975, American Medical Association

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Acute Myelogenous Leukemia Following
Fallout Radiation Exposure

ACUTE myelogenous leukemia developed in a 19-year-old Marshallese
man who had been exposed to radioactive fallout at 1 year of age. He was
one of 64 people on Rongelap Island
accidentally exposed in 1954 following the testing of an atomic device on
Bikini atoll 100 miles away. The acute
effects of exposure on this population
were hematological depression from
total body exposure to gamma radia-

arms, and legs, with spotty epilation of the
scalp. By six weeks, his leukocyte count
had dropped to 3,900/cu mm with depression of both neutrophil and lymphocyte
count, while his platelet count had reached
a low of 140,000/cu mm at 30 days. There
was gradual return of these blood elements
to near normal levels, He had remained
healthy with only the usual childhood dis-

and epilation from deposit of fallout
on the skin. There were no deaths,
and recovery occurred within a year.
Internal absorption of radionuclides
from inhalation and consumption of
contaminated food and water produced no acute effects, but absorption
of radioactive iodine resulted in later
development of thyroid lesions in one
third of the population; three of these
lesions were malignant. The highest
incidence was in children exposed at
less than 10 years of age, some of
whom had growth retardation.’

on a regimen of supplementary levothy-

eases until age 18, when benign adenomas

of the thyroid gland were detected and
surgically removed. He remained euthyroid with normal growth and development
roxine sodium treatment.
In September 1972, an annual examination showed his leukocyte count to be
2,000/eu mm. There were no other note-

worthy findings, and he appeared to be a
healthy, husky 19-year-old. Bone marrow
Fig 1.—Promyelocytes with Auer rods
(x 2,000).

Report of a Case
The man in this case report experienced
nausea, vomiting, and itching of the skin
during the first two days following exposure. By two weeks, transient beta-ray

burns developed on the skin over the neck,

From the Medical Research Center, Brookhaven National Laboratory, Upton, Long Island,
NY.
Reprint requests to Brookhaven National Laboratory, Upton, NY 11973 (Dr. Conard).

S5 ps Jung,30, 1975 @ Vol 232, No 13

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Brookhaven National Laboratory
Upten, L. L, New York

Robert A. Conard, MD

tion of 175 rads and beta-ray burns

he Medical Research Conter

examinations at Brookhaven National
Laboratory revealed acute myelogenous
leukemia (promyelocytic type with numerous Auer bodies) (Fig 1). Extensive antileukemic therapy was then begun at the
National Cancer Institute, but since compatible platelet transfusions were not
available to combat severe thrombocytopenia that developed, death from extensive
pulmonary bleeding intervened before a
remission could be achieved.
Comment

Retrospective examination of the
hematologic data obtained at frequent intervals since exposure is
noteworthy. Comparison of this patient’s peripheral blood leukocyte
counts (case 54) with the mean levels
of eight other boys exposed at less
than 5 years of age and eight unexposed Marshallese boys in the same
age rangeis plotted in Fig 2. The leukemia case showed greater depression of neutrophil count both during
the immediate postexposure period
and during subsequent years. Plots of
individual cases in the comparison
groups showed none with similarly

low levels. The platelets showed lesser
comparative depression, and the lymphocytes and erythrocytic elements
showed verylittle difference in the
leukemia case when compared with
the other groups. Other hematologic
data were generally normal (neutrophilic alkaline phosphatase level,
basophil counts, serum protein conAcute Myelogenous Leukemia—Conard

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