The authors report a case of recurrent strongyloidiasis in a former French
soldier of the Indochina colonial war (1946-54). Strongyloidiasis was assoc
iated with inaugural renal failure (acute steroid-resistant interstitial-ty
pe), requiring permanent hemodialysis. Despite antiparasitic treatment, rel
apse with digestive and pulmonary symptoms occured 10 years later, followin
g chronic eosinophilia. This observation emphasises that in dialysed subjec
ts, eosinophilia should always stimulate a search for parasitic etiologies
before incriminating dialysis-material allergy. Strongyloidiasis is a self
perpetuating helminthiasis whose distribution area is far greater than the
intertropical zone. It can be completely asymptomatic, appear as late diges
tive complications and be responsible for bacteraemic peaks with septic vis
ceral localizations. It causes a chronic oscillating eosinophilia. Diagnosi
s is usually performed by iterative stool examinations by Baermann techniqu
e in order to detect Strongyloides stercoralis rhabditoid larvae. In dialys
ed patients with unexplained eosinophilia awaiting renal transplant, the op
tions of systematic thiabendazole (50 mg/kg) or ivermectine (0.2 mg/kg) sin
gle-dose to overcame the risk of disseminated strongyloidiasis induced by i
mmunosupressive post-transplantation therapy could be debated.