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Fig 1.

Experimental model.

Tumor endoprostheses were embedded in water. Specifications and materials are indicated on the left. Central slices of coronal STIR and coronal T1-w MR pulse sequences are presented for each technique (standard; VAT, view-angle tilting; VAT&SEMAC, view-angle tilting and slice-encoding metal artifact correction).

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Table 1.

MR pulse sequences, experimental.

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Table 2.

Exemplary clinically applied MR pulse sequences.

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Fig 2.

True diameters of orthopaedic tumor endoprostheses.

True diameters were measured at six standardized spots as indicated and confirmed on original sketches (continuous lines). Asterisks indicate three standardized spots that were used for comparisons of different implant materials; broken lines indicate diameters that were additionally measured for this purpose.

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Fig 3.

Reduction of slice-encoding steps (SES) for slice-encoding metal artifact correction (SEMAC).

SES were reduced from 10 to 0 and assessed quantitatively and qualitatively. No SEMAC is equivalent to 0 SES. Acquisition time for all SES values is shown in the images. For qualitative evaluation, artifact diameters (mm) were measured on all MR images. VAT, view-angle tilting. SEMAC; slice-encoding metal artifact correction.

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Fig 4.

Quantitative results for coronal MR pulse sequences (STIR and T1-w sequences).

Diameter measurements were performed at six standardized levels on all MR images and compared to true diameters of the tumor endoprostheses. Study groups were a standard group (Standard) without application of VAT (view-angle tilting) or SEMAC (slice-encoding metal artifact correction) but otherwise identical pulse sequences, a group where VAT was applied (VAT; no SEMAC) and a group where both techniques, VAT and SEMAC, were applied (VAT&SEMAC). Mean values ±SEM are presented. True diameters were significantly smaller than artifact diameters in all groups (P<0.05).

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Table 3.

Quantitative measurements, experimental.

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Table 4.

Qualitative evaluation, experimental.

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Fig 5.

Coronal STIR images of one tumor endoprosthesis are presented for all groups (standard group; VAT (view-angle tilting) group; VAT&SEMAC (view-angle tilting and slice-encoding metal artifact correction) group).

Exemplarily, “A” indicates the interface between the collar of the stem and the stem of the prosthesis where the qualitative parameter “geometric distortion” was evaluated. “B” indicates the true position of the polyethylene component, which is interposed between the distal femoral component and the proximal tibial component of the endoprosthesis. “C” indicates the signal loss and signal pile-up artifacts at the edges of the prosthesis.

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Fig 6.

Example of the large size of the field of view.

A Large field of view is needed for postoperative follow-up MR imaging in tumor patients. MR imaging was performed in a young, female patient (15 years old) after resection of an osteosarcoma at the left distal femur and implantation of a combined femoral and tibial replacement. Pulse sequences presented include a coronal STIR sequence and a coronal T1-w sequence without and with contrast application and a subtraction image, all using view-angle tilting and slice-encoding metal artifact correction with 6 slice encoding steps.

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Fig 7.

Tumor recurrence.

Hip endoprosthesis with tumor recurrence of a chondrosarcoma in a 45 year old male patient. (A) a.p. radiograph; (B) Coronal contrast enhanced T1-w image with conventional artifact reducing MR techniques; (C) Coronal contrast enhanced T1-w image with VAT&SEMAC techniques.

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Table 5.

Initial diagnoses of the analyzed patient cohort.

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Fig 8.

Infection.

Posttraumatic pseudarthrosis at the left distal tibia with infection and intramedullary abscess formation in a 27 year old male patient with remaining cerclage fixation. (A) a.p. radiograph; (B) conventional coronal STIR image; (C) VAT&SEMAC coronal STIR image; (D) conventional coronal contrast enhanced T1-w image; (E) VAT&SEMAC contrast enhanced coronal T1-w image.

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Table 6.

Quantitative measurements, clinical.

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Table 7.

Qualitative evaluation, clinical.

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