As. Devriese et al., PITFALLS IN THE DIAGNOSIS OF HYPEREOSINOPHILIC SYNDROME - A REPORT OF2 CASES, Journal of internal medicine, 241(2), 1997, pp. 165-170
The idiopathic hypereosinophilic syndrome is empirically defined as th
e presence of prolonged eosinophilia without identifiable underlying c
ause, and with evidence of end-organ dysfunction. Virtually any organ
system may be involved, most frequently the heart, the central and per
ipheral nervous system, the lungs and the skin. We report two cases wh
ere the diagnosis of hypereosinophilic syndrome was proposed although
the classic criteria were not met. In the first case total peripheral
eosinophil counts were relatively low, but pathological evidence clear
ly showed infiltration of eosinophils in the damaged tissues. An hypot
hesis to explain this discrepancy is formulated. The second case did n
ot fulfil the first feature either, although the clinical presentation
and disease course corresponded well with other cases reported in the
literature. The delay in diagnosis was caused by early institution of
corticosteroids, clearing all evidence of eosinophil involvement in t
he observed tissue damage.