Gd. Sher et al., MYELODYSPLASTIC SYNDROME WITH PROLONGED RETICULOCYTE SURVIVAL MIMICKING HEMOLYTIC-DISEASE, American journal of clinical pathology, 101(2), 1994, pp. 149-153
A patient with myelodysplastic syndrome (refractory anemia) with marke
d and persistent reticulocytosis is presented. A referring diagnosis o
f hemolytic disease had been made. However, the Cr-51 red cell surviva
l was normal (T-1/2 24 days). Reticulocyte morphology, red cell creati
ne content, and in vitro reticulocyte survival studies have suggested
that the reticulocytosis arose as a consequence of delayed maturation
of the reticulocytes. Two patients with myelodysplastic syndrome and d
elayed reticulocyte maturation have previously been described; in both
patients, however, red cell survival was also shortened. Anemia with
reticulocytosis, mimicking hemolytic disease, may be an unusual presen
tation of myelodysplastic syndrome.