Purpose: Hydatid disease, a cyclo-zoonotic parasitic infestation cause
d by the larval stage of the cestode Echinococcus granulosus, is preva
lent worldwide. We reviewed the clinical findings of a large series of
renal hydatidosis treated in an endemic area with special emphasis on
diagnostic pitfalls. Materials and Methods: A retrospective 15-year r
eview in a rural area of central Spain (600,000 population), with a gl
obal incidence of hydatidosis of 10 new cases per 100,000 population p
er year, revealed 34 with renal echinococcosis treated surgically (3 t
o 4% of officially confirmed cases of hydatidosis). Clinical, radiolog
ical and laboratory data were analyzed. Results: Renal hydatid disease
mimicked other diseases. The combination of clinical history, imaging
studies, and serological and urine investigation yielded a reliable p
retreatment diagnosis in only 50% of cases and a presumptive diagnosis
in 71%. Among imaging studies computerized tomography was the most va
luable diagnostic examination. Moderate eosinophilia was found in half
of the cases, while a third had scoleces in the urine. A diagnostic a
nd therapeutic algorithm is presented. Conclusions: Preoperative diagn
osis of renal hydatid disease is difficult even in an endemic zone. Im
aging studies are suggestive but usually inconclusive, and the differe
ntial diagnosis with a renal tumor or complicated cyst may not be made
without surgery. Renal sparing surgery is possible in a significant p
roportion of cases, particularly when preoperative diagnosis has been
considered. Significant surgical morbidity can be expected, and the ri
sk of anaphylaxis and hydatid seeding, although low, should not be ove
rlooked.