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Clin Orthop Relat Res. 2013 Jul;471(7):2078-82. doi: 10.1007/s11999-012-2780-y. Epub 2013 Jan 5.

Severe metal-induced osteolysis many years after unipolar hip endoprosthesis.

Author information

1
Division of Orthopaedic Surgery, McGill University, Montreal, QC, Canada.

Abstract

BACKGROUND:

Modularity of the femoral head-neck junction provides increased intraoperative flexibility to the surgeon. Complications of this modularity include damage to the trunnion, with subsequent bone and/or soft tissue loss from adverse reactions to metal debris.

CASE DESCRIPTION:

We describe two cases of severe metal-induced osteolysis and soft tissue damage requiring revision 10 and 13 years following implantation of a unipolar endoprosthesis. Damage to the trunnion resulted in severe acetabular and trochanteric osteolysis and soft tissue loss requiring complex revision surgery.

LITERATURE REVIEW:

Several reports have shown the trunnion, the head-neck interface, and the neck-stem couple as the causes of this early failure secondary to metal ion release from mechanical fretting corrosion or from crevice corrosion at these modular interfaces. These reports have been in association with a total hip prosthesis rather than a unipolar endoprosthesis. Revision of a unipolar endoprosthesis is most commonly attributable to stem loosening or acetabular erosion from the large femoral head articulating on the host acetabular cartilage and not owing to failure of the trunnion.

PURPOSES AND CLINICAL RELEVANCE:

Trunnion damage resulting in a severe reaction to metal debris with acetabular osteolysis, erosion of the greater trochanter, and loss of the abductor mechanism can occur years after implantation of a cementless unipolar endoprosthesis. This raises questions regarding long-term safety of the modular interface of a contemporary cementless stem and a large-diameter unipolar head. We recommend long-term followup of patients with a unipolar endoprosthesis as early recognition and treatment are required to avoid a potentially complex revision.

PMID:
23292889
PMCID:
PMC3676628
DOI:
10.1007/s11999-012-2780-y
[Indexed for MEDLINE]
Free PMC Article
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