BACKGROUND: Abnormalities of the long arm of chromosome 3 (3q) involving ba
nds 3q21 and/or 3q26 occur in 2-6% of myeloid malignancies. Trilineage myel
odysplasia, especially in the megakaryocytic line, is a characteristic feat
ure. Additional abnormalities of chromosomes 5 and 7 are usually present. T
he response to treatment and prognosis are poor.
PATIENTS AND METHODS: The main clinical, cytologic (bone marrow aspirate an
d biopsy) and cytogenetic characteristics as well as the response to the tr
eatment in 10 patients with 34 abnormalities diagnosed in a single hospital
in a period of 8 years are referred.
RESULTS: Eight patients had acute non-lymphoblastic leukemia, being de nova
in five of them. The median value of hemoglobin was 87 g/l (range: 51-148)
, white blood cells count 5.8 x 10(9)/l (1.2-47.1) and platelet count 34 x
10(9)/l (5-182), The morphological findings in the study of the bone marrow
were: dyserythropoietic features (7 patients), dysgranulopoietic abnormali
ties (5 patients) and small-sized megakaryocytes with hypolobulated nuclei
(8 patients). Fibrosis was observed in the 4 cases in which a bone marrow b
iopsy was performed. In addition to the 3q alteration, abnormalities of chr
omosomes 7 (4 patients), 5q (2 patients) and +8 (2 patients) were present.
Four patients received intensive chemotherapy and in two of them a complete
remission was achieved, but relapse occurred at 3 and 5 months, respective
ly. All patients have died, the median survival being 7 months.
CONCLUSIONS: 34 abnormalities define a subtype of myeloid malignancies with
characteristic clinical and morphological features. The response to therap
y and survival are poor.