I. Lorand-metze et al., Magnetic resonance imaging of femoral marrow cellularity in hypocellular haemopoietic disorders, CLIN RADIOL, 56(2), 2001, pp. 107-110
AIM: Magnetic resonance imaging (MRI) of the femora was used to investigate
the marrow cellularity during the evolution of non-transplanted aplastic a
naemia (AA) and hypocellular myelodysplastic syndrome (h-MDS) in order to i
nvestigate the relationship between this cellularity and disease progressio
n.
METHODS: Magnetic resonance imaging was performed in adult patients with pa
ncytopaenia and hypocellular bone marrow. Coronal T1 weighted and STIR imag
es were obtained, and analysed semiquantitatively. These data were compared
with diagnosis, peripheral blood counts and bone marrow histology at diagn
osis and at the time of the MRI examination.
RESULTS: Patients were examined 2-84 months after diagnosis (median, 16 mon
ths). In AA, 11/13 patients showed a fatty, faint or nodular pattern. In h-
MDS, the majority of the patients (10/14) had a scattered or uniform signal
pattern. In AA, a significant correlation was found between the degree of
femoral cellularity and disease duration. Only three cases had diffuse high
signal on STIR: among them, one had paroxysmal nocturnal haemoglobinuria a
nd the other developed acute leukaemia 3 months after MRI examination. Four
patients have died: three with h-MDS presenting a scattered (two cases) or
a uniform (one case) MRI signal and one with AA (with a nodular pattern).
CONCLUSION: In AA, femoral haemopoiesis is usually not pronounced, and if p
resent, does not contribute to the improvement of blood counts. In h-MDS, p
atients with discrete femoral haemopoiesis had an improvement in their bloo
d counts with disease duration, similar to that found in AA. Conversely, in
patients with pronounced femoral cellularity, blood counts remained stable
or had deteriorated since diagnosis. This favours the hypothesis that, as
is observed in MDS with a hypercellular marrow, scattered or uniform marrow
patterns in femoral MRI are signs of more aggressive disease. Lorand-Metze
, I. et al. (2001) Clinical Radiology 56, 107-110. (C) 2001 The Royal Colle
ge of Radiologists.