The first generation hip resurfacing arthroplasty (HRA) developed in the 1970s used a cobalt-chromium or titanium alloy femoral component bearing against a polyethylene metal-backed acetabular component. These HRAs generated large volumes of polyethylene wear debris [18] and were highly susceptible to osteolysis and, because of this, they were largely abandoned. The reintroduction of metal-on-metal (M-M) bearings in THAs [36] has encouraged their use in HRA as well [1, 28]. One design, the Birmingham Hip Resurfacing (BHR), has been in wide use in the United Kingdom, Europe, and Australia for a decade [34] and received FDA approval for use in the United States in 2006. A dozen or more HRA designs are available in Europe; some of these are undergoing clinical trials and are pending FDA approval for use in the United States. Targeted to young and active patients, HRAs are expected to account for an increasing number of hip arthroplasties in the future [5]. Thus, it is important to understand the limitations and complications associated with these devices before their widespread use.
Femoral neck fractures and aseptic loosening account for the majority of HRA failures [6, 12] whereas, unlike their historical metal-polyethylene predecessors, osteolysis is not a common cause of failure in modern M-M HRAs [2, 19, 34]. This is consistent with their ability to operate with very low wear if factors such as surface smoothness and diametric clearance (the difference between the diameters of the femoral head and acetabular cup) are optimized [17, 32]. However, it is becoming evident that socket placement outside of a recommended range (30° to 50° abduction and 15° to 25° of anteversion) [9, 10, 23] can lead to a greater amount of metal release, particularly in small-diameter components [10, 22, 29]. Under such conditions, large quantities of particulate cobalt-chromium debris and associated corrosion products can lead to a variety of adverse reactions, including osteolysis [6, 9], periprosthetic soft tissue masses [9, 13, 14] and extensive necrosis [4, 29].
Recent reports from one large-volume resurfacing surgery center described “pseudotumors” forming in the hips of some female patients with M-M HRAs [30] which led the authors to speculate that a preoperative sensitization to metal may be a factor. This complication was estimated to occur in 1% of patients undergoing HRA within 5 years, but the incidence could be higher with longer followup and in patients with bilateral implants [25]. Subsequent studies by this group reported higher metal wear in patients with pseudotumors compared to patients without pseudotumors [20]. Pseudotumor-like, enlarged, fluid-filled bursae in HRAs with malpositioned acetabular components had been previously reported by our group [6, 9] and others [8]. However, pseudotumor-like reactions have also been reported in M-M HRAs without evidence of high wear or metal hypersensitivity [27] as well as in non-M-M bearing hips [16, 24]. The histology of pseudotumors includes features consistent with metal wear reactions (eg, macrophages with particles [9, 30]) as well as metal hypersensitivity (eg, lymphocytic aggregates, granulomas [26, 31]) although both may occur together or extensive necrosis may prevent detailed histological characterization [31].
The aim of this study was to compare the histopathologic features (synovial lining integrity, inflammatory cell infiltrates including lymphocytes, macrophages, plasma cells, giant cells, as well as tissue organization, necrosis and metal wear particles) in pseudotumor-like tissues from M-M hips revised for suspected high wear with pseudotumor-like tissues from M-M hips revised for unexplained pain and suspected metal hypersensitivity.
We selected from archived M-M hip retrievals 32 specimens that were submitted with an unusual soft tissue reaction described by the revising surgeons as an aseptic “soft tissue mass,” “enlarged bursa,” or a “cyst” which could be considered as “pseudotumor-like.” Twenty-seven of the 32 cases were hip resurfacings (four articular surface replacements (ASR, DePuy International, Leeds, UK), 20 Birmingham Hip Resurfacings (BHR, Smith and Nephew, Memphis, TN), two Conserve Plus hip resurfacings (Wright Medical Technology, Memphis, TN), and one McMinn resurfacing (Corin, Cirencester, UK). The remaining five cases were conventional total hip arthroplasties (one Biomet M2 THA, Biomet, Warsaw, IN), one big femoral head THA (Wright Medical Technology), and three Metasul bearing total hips (Zimmer, Warsaw, IN). There were 23 females and nine males with average ages of 54 years (range, 18–68 years) and 62 years (range, 48–82 years), respectively. As documented by the revising surgeons, the reasons for revision were acetabular malposition (steep abduction angle, excessive or insufficient anteversion, n = 15), unexplained pain (i.e., in the absence of infection, radiographic loosening or malposition, and where metal sensitivity was suspected, n = 9), and aseptic loosening (n = 5).
We calculated the wear depth of 24 of the 32 explanted components including HRAs that had not been sectioned and were still intact by digitizing 300 to 400 points on the bearing surface with a coordinate measurement machine (BMT 504; Mitotoyo, Aurora, IL). The remainder had been sectioned without prior wear measurements for a separate study. The resolution of this equipment was approximately 4 μm, so wear depths at or below this level were considered “undetectable.” Acetabular cup abduction angles were measured by the revising surgeons on AP radiographs in 28 of the 32 cases using standard radiographic techniques [33] (four cases had poor-quality radiographs deemed unsuitable for this analysis). This involved measuring the angle between a line connecting the ischial spines and another line drawn tangent to the opening of the cup, representing the large diameter of the ellipse. This method is widely used in clinical practice for postoperative measurement of cup position [35].
|
Points |
Synovial lining |
|---|---|
|
0 |
Intact synovial lining |
|
1 |
Focal loss of synovial surface, fibrin attachment may occur |
|
2 |
Moderate to marked loss of synovial surface, fibrin attachment |
|
3 |
Complete loss of synovium, abundant attached fibrin and /or necrosis of lining tissue |
|
Points |
Inflammatory infiltrate |
|---|---|
|
0 |
Minimal inflammatory cell infiltrates |
|
1 |
Predominantly macrophages, occasional lymphocytes may occur |
|
2 |
Mix of macrophages and lymphocytes, either diffuse and/or small (< 50% of hpf) perivascular aggregates |
|
3 |
Mix of macrophages and lymphocytes, large (> 50% hpf) perivascular aggregates may occur |
|
4 |
Predominantly lymphocytes, mostly in multiple, large (> 50% hpf) perivascular aggregates, follicles may be present |
|
Points |
Tissue organization |
|---|---|
|
0 |
Normal tissue arrangement |
|
1 |
Mostly normal tissue arrangement, small areas of synovial hyperplasia, focal necrosis may occur |
|
2 |
Marked loss of normal arrangement, appearance of distinct cellular and acellular zones, thick fibrous layers may occur |
|
3 |
Perivascular lymphocytic aggregates mostly located distally, thick acellular areas may occur |
|
Sum |
|
|
Low = 0–4 |
|
|
Moderate = 5–8 |
|
|
High = 9–10 |
The independent variable considered in this study was whether the patients were revised with suspected high wear or with suspected metal hypersensitivity. The dependent variables were the histologic features related to the intensity of the inflammatory reaction: ALVAL score, lymphocytes, macrophages, plasma cells, giant cells, necrosis, and metal particles. Univariate analysis was used to determine the mean, median, SD, and distribution for each variable as necessary. The Mann-Whitney test was used to compare the femoral wear and wear rate of patients with suspected high wear with those suspected to have metal hypersensitivity. Likewise, histologic ratings for ALVAL were compared in these two groups. The Mann-Whitney test was determined to be appropriate because the dependent variables were not normally distributed.
|
Variable (p value) |
Suspected wear related |
Suspected metal sensitivity |
||
|---|---|---|---|---|
|
Average |
SD |
Average |
SD |
|
|
ALVAL score (p < 0.001) |
3.6 |
2.5 |
8.5 |
1.4 |
|
Macrophages (p < 0.001) |
2.7 |
0.5 |
1.7 |
0.5 |
|
Lymphocytes (p = 0.001) |
1.4 |
0.6 |
2.5 |
0.7 |
|
Metal particles (p = 0.008) |
1.5 |
0.7 |
0.7 |
0.5 |
|
Necrosis (p = 0.29) |
1.0 |
0.7 |
1.4 |
0.7 |
|
Tidemark (p = 0.03) |
0.2 |
0.4 |
0.7 |
0.5 |
|
Layering organization (p = 0.024) |
0.28 |
0.5 |
0.8 |
0.4 |
The average femoral wear rate for the components from patients revised for suspected high wear was 19.9 microns per year (standard deviation 18.1, range 3.1–76.2 microns per year) and was higher (p = 0.003) than that for components from patients revised for pain and suspected metal sensitivity (average 3.7, SD 2.2, range 1.5–6.7 microns per year).
Pseudotumors, masses and enlarged bursae have been reported in hips with M-M bearings associated with pain and swelling. The cause of these reactions is unclear but several authors have suggested it is a reaction to high wear [20, 30] or to metal hypersensitivity [15, 26, 30]. This study was conducted to compare the histology of pseudotumor-like tissues from hips suspected to have high wear with those from patients with pain and suspected metal sensitivity and our results support the formation of pseudotumors from both wear and hypersensitivity reactions.
We acknowledge several major limitations. First, we did not provide any specific morphologic criteria for the tissue specimens we studied because we were confident experienced orthopaedic surgeons would recognize an unusual, adverse reaction. For this reason, we have used the term “pseudotumor-like” and we are confident that the submitted specimens, even though labeled as masses, cysts or enlarged bursae, were comparable to the cystic or solid pseudotumors described by Pandit et al. [30]. Similar histological features were noted in pseudotumor and pseudocapsule tissues in our analysis (results not shown), a finding also reported by Mahendra et al. [26]. Thus, even if some of our samples were actually misclassified thickened capsules, the results of our analysis remain valid. Second, we cannot prove a presumptive diagnosis of metal sensitivity. Unlike component wear or serum ion levels, which can be measured with a known degree of accuracy, there are currently no definitive blood tests or histopathologic criteria to diagnose metal hypersensitivity. However, we devised a working postulate to diagnose hypersensitivity: early onset of pain, the absence of other reasons for pain (such as loosening, impingement, infection, or high wear), and the resolution of symptoms after the removal of the cobalt-chromium components. Other clinical reports have noted similar features in patients suspected to have a metal hypersensitivity reaction [7, 37]. We recognize that it is possible for metal hypersensitivity to coexist with any of these other causes of pain and we also recognize that there is variability in the clinical presentation that will confound this working definition. Third, we observed a range of intra- and interobserver statistics for light microscopic tissue features. This is to be expected given that we were using a semiquantitative scoring system and that the importance of histologic features is subject to individual interpretation. The histologic rating is meant to be used in conjunction with the case history, radiographic findings, and retrieval findings and when so used, the interpretation of histologic features is more likely to predict their cause.
Our semiquantitative analyses demonstrated substantial differences in the histological features of pseudotumor-like tissues from patients with high wear compared with those tissues from patients suspected to have metal hypersensitivity. The tissues from both groups contained macrophages and lymphocytes in variable amounts and distributions but applying the ALVAL rating allowed clear patterns to emerge. In particular, there was generally less disruption of the synovial surface, and greater preservation of the normal tissue architecture in the high wear group. In contrast, the most extensive damage to the tissues and the densest lymphocyte aggregates occurred in patients suspected to have a metal hypersensitivity reaction and typically this occurred in the absence of high wear. The variability we noted is consistent with other histologic reports; Pandit et al. [30] noted scattered, focally heavy macrophage and lymphocytic infiltrates, including lymphoid aggregates, in formal biopsy samples of pseudotumors from 10 hip resurfacings revised for pain and/or pseudotumor formation. Metal particles were present but not prominent in the tissues. Similar findings were reported in two female patients with masses causing femoral neuropathy around unilateral hip resurfacings [15]. Wear measurements were not provided for the implants associated with these pseudotumors and it is not clear if the patients had risk factors for high wear such as small component size and implant malposition.
One recent study by Langton et al. [21] analyzed tissues from 17 patients with M-M hips following revision for an adverse response to metal debris including pseudotumor formation. They reported substantially higher component wear and blood ion levels in these patients compared with those revised for other reasons. Their histological examination noted ALVAL features such as synovial ulceration and perivascular lymphocytes which ranged from absent to moderate. The lack of lymphocytes in some of their cases and the absence of high levels of lymphocytic infiltrates in this group of patients with high wear is consistent with our observations. We suggest that using the ALVAL score will promote more standardized reporting of the histological features of tissues removed from M-M hips.
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