Refractory thrombocytopenia (RTC) is a counter-concept to refractory anemia
, which is characterized by isolated thrombocytopenia associated with clona
l chromosomal abnormality. The diagnosis of RTC is difficult to establish b
ased on morphologic features alone. And steroid therapy for RTC is often in
effective. We examined 3 patients with RTC to identify its characteristics
and measured serum thrombopoietin levels. The mean platelet count was 5.1 x
10(4)/mu l and the mean age was 64 years. None of our patients had clinica
l nor laboratory evidence of liver dysfunction, renal disease or disseminat
ed intravascular coagulation. All patients were negative for antiplatelet a
ntibody, PA-IgG and anticardiolipin-beta 2GPI antibody. Leukocyte alkaline
phosphatase level was low in two patients, Clonal chromosomal abnormalities
of different types were detected in all patients. Bone marrow smears showe
d micromegakaryocytes. But there were no apparent morphological abnormaliti
es of erythroid and granuloid series. Thrombopoietin levels, as determined
by enzyme-linked immunosorbent assay, varied from <0.2 to 1.40 fmol/ml. We
could not find the screening tool of RTC. In conclusion, there is a need to
identify RTC from isolated thrombocytopenia because the patients with RTC
don't have good prognosis as patients with isolated thrombocytopenia. Cytog
enetic analysis is necessary to establish the diagnosis of RIG. We recommen
d that a patient above 50 years of age presenting with isolated thrombocyto
penia and a low leukocyte alkaline phosphatase score should be suspected of
having RTC. Am. J. Hematol. 62:103-105 1999. (C) 1999 Wiley-Liss, Inc.