Purpose: Skeletal manifestation of alveolar (E. multilocularis) or cystic (
E. granulosus) echinococcosis is seldom, with an incidence of less than 2%
of all cases. By reporting on a rare case of bony manifestation of E. granu
losus, we intend to emphasize current standards in surgical and drug manage
ment of the disease. Typical radiographic and blood-chemistry findings are
highlighted on a 62-year-old Arabiqu female suffering from a cystic echinoc
occosis with skeletal manifestation in the left ileum and lower lumbar spin
e. Results: Radiographically typical are fine zones of osteolysis which, at
a later stage, show confluence. Due to the rigid structure of cortical bon
e, cysts tend to grow slowly, and seldom exceed 2cm in diameter. Only after
having broken through the cortical bone, may a massive increase in size be
observed. By means of serological tests, it is postoperatively possible to
evaluate how successful radical surgery with removal of larvae was. Furthe
rmore, serological tests can be used as a screening method, offering a diag
nostic tool that can also utilized in detecting a recurrence. Conclusion: T
he surgical aim in the treatment of osseous echinococcosis should be in acc
ordance to curative tumor surgery. Even after radical removal of the parasi
tes, the WHO suggests an adjuvant chemotherapy with mebendazole or albendaz
ole for at least two years after surgery. In cases where only a palliative
treatment is possible, the antihelminthic drug administration can be contin
uous.