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AJR 2002; 179:657-663
© American Roentgen Ray Society


Original Report

Rapidly Destructive Osteoarthritis of the Hip: MR Imaging Findings

Nathalie Boutry1, Christelle Paul1, Xavier Leroy2, David Fredoux1, Henri Migaud3 and Anne Cotten1

1 Department of Radiology, Hôpital Roger Salengro, Blvd. du Professeur Leclercq, CHRU de Lille, 59037 Lille Cedex, France.
2 Department of Pathology, Hôpital Roger Salengro, CHRU de Lille, 59037 Lille Cedex, France.
3 Department of Orthopaedics, Hôpital Roger Salengro, CHRU de Lille, 59037 Lille Cedex, France.

Received September 24, 2001; accepted after revision March 13, 2002.

 
Address correspondence to N. Boutry.


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The aim of our study was to describe the MR imaging findings in patients with rapidly destructive osteoarthritis of the hip.

CONCLUSION. The key MR imaging features of rapidly destructive hip osteoarthritis include joint effusion (100%), bone marrow edemalike pattern in the femoral head and neck (100%) or acetabulum (83%) or both, femoral head flattening (92%), and cystlike subchondral defects (83%). Additional findings are low-signal-intensity lines (33%) in the femoral epiphysis, bandlike areas of low signal intensity in the upper pole of the femoral head (8%), and focal signal abnormalities in the adjacent soft tissues (33%) on short tau inversion recovery MR images, fat-suppressed T2-weighted MR images, and fat-suppressed gadolinium-enhanced T1-weighted MR images.


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Rapidly destructive osteoarthritis of the hip is a unique hip disorder characterized by rapid chondrolysis (> 2 mm in 1 year or 50% joint-space narrowing in 1 year) and no evidence of other forms of rapidly destructive arthropathy [1]. Clinical history and follow-up radiographs are sufficient for making the diagnosis in most cases. However, less typical features could cause diagnostic problems. MR imaging may offer an alternative noninvasive technique for evaluating this condition. Little information is available on MR imaging findings in patients with rapidly destructive hip osteoarthritis [2, 3]; to our knowledge, no other series has described the MR imaging findings of this disorder.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
We retrospectively reviewed MR images of 12 patients in whom rapidly destructive hip osteoarthritis was diagnosed. These cases occurred over an 8-year period. Patients were included in this study if they satisfied the accepted diagnostic criteria for rapidly destructive hip osteoarthritis [1], which were based on results of history, conventional radiography, and the clinical course of the disease. In seven patients, histopathologic confirmation was available. Specifically, before MR imaging, all patients presented with rapid progression of hip pain. In all patients, analyses of initial and follow-up radiographs showed rapid joint destruction within 1 year. Patients were excluded if they had a history of other conditions that might result in destructive hip arthropathy, including septic arthritis, inflammatory arthritis, osteonecrosis with secondary osteoarthritis, pyrophosphate-associated arthropathy, and neuropathic osteoarthropathy.

The 12 patients who satisfied these criteria comprised four men and eight women. The mean age at presentation was 74 years, ranging from 47-81 years. All patients had hip pain (five, on the right; seven, on the left) with a duration of symptoms ranging between 3 months and 1 year (mean, 7 months) before MR imaging. One of the 12 patients had bilateral disease; MR imaging of only one hip was performed in this patient. The major complaints of the patients were pain (n = 11) and restricted movement (n = 5).

Before MR imaging, the possibility of rapidly destructive hip osteoarthritis was suspected in seven patients. However, clinical findings simulated those of other diseases such as osteonecrosis (n = 6), spontaneous fracture (n = 3), septic arthritis (n = 2), and transient osteoporosis (n = 1), and for this reason, MR imaging was performed in all patients. The time between the first radiography and MR imaging ranged from 2 to 12 months (mean, 6 months). Synovial fluid analysis was available in two patients who had been suspected of having septic arthritis; the results of bacteriologic studies in these patients were negative.Go,Go



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Fig. 1A. Rapidly destructive hip osteoarthritis in 68-year-old woman with right-sided hip pain. Anteroposterior radiograph obtained at onset of symptoms shows moderate superolateral joint-space narrowing and small subchondral cystic lesion in acetabulum.

 


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Fig. 1B. Rapidly destructive hip osteoarthritis in 68-year-old woman with right-sided hip pain. Anteroposterior radiograph obtained 6 months after A shows superior loss of joint space, flattening of femoral head, and heterogeneous bone aspect.

 

Follow-up radiographs and clinical reports were available for review in all patients. Anteroposterior views of the pelvis and anteroposterior and lateral views of the symptomatic hips depicted progressive joint destruction in all patients. In 11 patients, radiographs showed narrowing of the superolateral joint space, whereas the superomedial part of the joint was involved in one patient. Additional findings included varying degrees of subchondral sclerosis, subchondral cyst formation, bone destruction, and mild osteophytosis. Furthermore, anteroposterior views of the knees had been obtained in all patients; these showed no chondrocalcinosis. None of our patients had a history of polyarthritis. However, four patients showed characteristic changes of osteoarthritis in the contralateral hip (n = 2) and the knees (n = 2). In one patient, clinical reports mentioned degenerative changes in the spine. All patients underwent total hip replacement resulting in relief of symptoms. At no time did any of them receive antibiotics. Resected femoral head specimens were available in seven patients.Go,Go



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Fig. 2A. Rapidly destructive hip osteoarthritis in 57-year-old man with right-sided hip pain. Anteroposterior radiograph obtained at onset of symptoms shows moderate joint-space narrowing and subchondral sclerosis.

 


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Fig. 2B. Rapidly destructive hip osteoarthritis in 57-year-old man with right-sided hip pain. Anteroposterior radiograph obtained 3 months after A reveals superior joint-space narrowing. Mild subchondral bone sclerosis is seen with no osteophytes.

 

Field strength for the MR imaging ranged from 0.5 to 1.5 T. All protocols included T1-weighted MR imaging of the symptomatic hips, both in the coronal and sagittal planes. All patients received IV gadolinium contrast material. Fat-suppressed gadolinium-enhanced T1-weighted MR images were obtained in 11 patients. Short tau inversion recovery images or fat-suppressed T2-weighted images of the involved hips were obtained in coronal (n = 8) and sagittal (n = 6) planes.

The MR imaging studies were retrospectively reviewed by two experienced musculoskeletal radiologists. Consensus agreement was achieved. Data recorded from MR imaging studies included the presence or absence of a joint effusion, synovitis, and signal intensity changes in bone marrow and soft tissues. Effusion was assumed when areas of high signal intensity were found in the joint space on T2-weighted MR images. The amount of joint fluid was graded from 0 to 3 according to the staging system described by Mitchell et al. [4]: 0, none; 1, minimal; 2, enough fluid to surround the femoral neck; and 3, sufficient fluid to distend the joint capsule. Synovitis was diagnosed by comparing unenhanced and contrast-enhanced T1-weighted MR images for linear or curvilinear enhancement in the site of the normal synovium. Synovial membrane hypertrophy was subjectively graded with a 3-point scale: 0, absent; 1, moderate; 2, frank synovitis. Other MR imaging findings were recorded, including information regarding the additional subchondral findings.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
All 12 patients (100%) had hip joint effusion (grade 2 fluid [n = 2]; grade 3 fluid [n = 10]). In two patients (17%), three intraarticular loose bodies were shown on MR imaging. All 12 patients had evidence of synovitis on MR images (moderate [n = 3]; frank [n = 9]) (Figs. 1C and 1D).



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Fig. 1C. Rapidly destructive hip osteoarthritis in 68-year-old woman with right-sided hip pain. Coronal (C) and sagittal (D) fat-suppressed gadolinium-enhanced T1-weighted MR images (TR/TE, 720/20) obtained 6 months after onset of symptoms show frank synovitis (curved arrow). Note presence of cystlike subchondral defects (straight arrows) at weight-bearing surfaces of femoral head and acetabulum.

 


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Fig. 1D. Rapidly destructive hip osteoarthritis in 68-year-old woman with right-sided hip pain. Coronal (C) and sagittal (D) fat-suppressed gadolinium-enhanced T1-weighted MR images (TR/TE, 720/20) obtained 6 months after onset of symptoms show frank synovitis (curved arrow). Note presence of cystlike subchondral defects (straight arrows) at weight-bearing surfaces of femoral head and acetabulum.

 

MR imaging of the bone marrow edema pattern, an ill-defined marrow area of low signal intensity on T1-weighted MR images and of high signal intensity on short tau inversion recovery images or on fat-suppressed T2-weighted images, was identified in the femoral head in 12 patients (100%) and in the acetabulum in 10 patients (83%) (Figs. 2C and 2D). In all 12 patients, diffuse signal abnormalities were found in the marrow of the femoral head and neck, with frequent (10 patients) abnormal findings extending into the intertrochanteric area (Fig. 3D). An edemalike abnormality on MR imaging, however, was more prominent at the weight-bearing areas (nine patients).



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Fig. 2C. Rapidly destructive hip osteoarthritis in 57-year-old man with right-sided hip pain. Coronal T1-weighted MR image (TR/TE, 552/14) obtained 4 months after onset of symptoms shows ill-defined low-signal-intensity area in femoral head and, to lesser degree, in acetabulum.

 


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Fig. 2D. Rapidly destructive hip osteoarthritis in 57-year-old man with right-sided hip pain. Sagittal short tau inversion recovery MR image (5216/60; inversion time, 150 msec) obtained 4 months after onset of symptoms shows ill-defined high-signal-intensity area in femoral head.

 


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Fig. 3D. Rapidly destructive hip osteoarthritis in 72-year-old woman with left-sided hip pain. Coronal short tau inversion recovery MR image (5216/60; inversion time, 150 msec) obtained 5 months after onset of symptoms reveals markedly increased signal intensity in femoral head and neck and grade 3 amount of fluid in joint. Note low-signal-intensity line (arrows) in upper pole of femoral head.

 

Findings in 11 patients (92%) showed evidence of femoral head flattening (severe in two patients) at the weight-bearing surfaces associated with superolateral subluxation in eight patients (67%). MR imaging revealed small marginal osteophytes along the femoral neck and the anterolateral aspect of the acetabulum in 10 patients (83%) and in two patients (17%), respectively.

Miscellaneous subchondral changes were also observed on MR images. Findings in one patient (8%) showed evidence of a low-signal-intensity subchondral area on T1-weighted, T2-weighted, and contrast-enhanced T1-weighted MR images. This abnormality was located at the superior pole of the femoral head (Figs. 4C and 4D). In four patients (33%), the femoral head exhibited thin lines of low signal intensity on both T1- and T2-weighted MR images (Figs. 3D and 3E). These lesions coursed parallel to the articular surface and were suggestive of subchondral fractures. In 10 patients (83%), cystic defects were depicted in areas adjacent to the subchondral bone plate (Figs. 1C and 1D). Typically, these cysts were located at the weight-bearing surfaces of femoral head and acetabulum; they ranged from 2 to 15 mm in diameter and exhibited high signal intensity on T2-weighted or gadolinium-enhanced T1-weighted MR images.Go,Go,Go



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Fig. 4C. Rapidly destructive hip osteoarthritis in 73-year-old-woman with right-sided hip pain. Sagittal short tau inversion recovery MR image (TR/TE, 5216/60; inversion time, 150 msec) (C) and sagittal fat-suppressed gadolinium-enhanced T1-weighted MR image (612/14) (D) obtained 7 months after onset of symptoms show increased signal intensity in femoral head and acetabulum with low-signal-intensity subchondral area (arrowheads) in upper pole of femoral head.

 


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Fig. 4D. Rapidly destructive hip osteoarthritis in 73-year-old-woman with right-sided hip pain. Sagittal short tau inversion recovery MR image (TR/TE, 5216/60; inversion time, 150 msec) (C) and sagittal fat-suppressed gadolinium-enhanced T1-weighted MR image (612/14) (D) obtained 7 months after onset of symptoms show increased signal intensity in femoral head and acetabulum with low-signal-intensity subchondral area (arrowheads) in upper pole of femoral head.

 


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Fig. 3E. Rapidly destructive hip osteoarthritis in 72-year-old woman with left-sided hip pain. Sagittal fat-suppressed gadolinium-enhanced T1-weighted MR image (729/14) obtained 5 months after onset of symptoms shows increased signal intensity in subchondral areas of femoral head and acetabulum. Note low-signal-intensity line (arrows) in upper pole of femoral head.

 


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Fig. 3A. Rapidly destructive hip osteoarthritis in 72-year-old woman with left-sided hip pain. Anteroposterior radiograph obtained at onset of symptoms shows no significant joint-space narrowing and small lateral acetabular osteophyte.

 


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Fig. 3B. Rapidly destructive hip osteoarthritis in 72-year-old woman with left-sided hip pain. Anteroposterior radiograph obtained 6 months after A shows superior joint-space loss and small osteophytes on lateral aspect of femoral head and acetabulum.

 


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Fig. 3C. Rapidly destructive hip osteoarthritis in 72-year-old woman with left-sided hip pain. Sagittal T1-weighted MR image (TR/TE, 480/14) obtained 5 months after onset of symptoms shows abnormally low signal intensity in superior parts of both femoral head and acetabulum. Note joint-space narrowing.

 

In four patients (33%), short tau inversion recovery, fat-suppressed T2-weighted, or fat-suppressed gadolinium-enhanced T1-weighted MR images showed signal abnormalities in the adjacent soft tissues (Fig. 5C).



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Fig. 5C. Rapidly destructive hip osteoarthritis in 73-year-old-woman. Coronal fat-suppressed gadolinium-enhanced T1-weighted MR image (TR/TE, 720/18) obtained 4 months after onset of symptoms shows high-intensity signal in femoral neck and acetabulum. Note focal signal abnormalities (arrows) of soft tissues.

 

Resected femoral head specimens were available in seven patients. No evidence of primary osteonecrosis, inflammatory arthritis, or crystal deposition was observed in these specimens. The pathologist made the diagnosis of osteoarthritic changes in all patients. On microscopic examination, all specimens exhibited severe degenerative changes in the cartilage and subchondral bone sclerosis. Hypervascularity was a frequent finding (n = 6) in the subchondral bone (Fig. 1E). Abnormal trabeculae, either thickened (n = 3) or thinned (n = 4), were commonly observed in the subarticular region. Subchondral defects were identified in three patients; the defects contained fibroconnective tissue (n = 2) or mucoid degeneration (n = 1). All sections of the femoral head showed normal fatty bone marrow with spotty remnants of hematopoietic marrow. In three of the four patients with findings of epiphyseal lines on MR imaging, histologic examination revealed trabecular fractures in the vicinity of the articular surface. Small marginal osteophytes were identified in three cases. Less striking histologic findings included foci of fibrosis, interstitial edema and hemorrhage in the marrow spaces, focal marrow fat necrosis, and areas of reactive bone formation and bone resorption. Sections of the synovium were available in six patients; four of these showed reactive changes.



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Fig. 1E. Rapidly destructive hip osteoarthritis in 68-year-old woman with right-sided hip pain. On moderate microscopic examination, photomicrograph of histologic section shows prominent hypervascularity in subchondral bone. Note presence of numerous capillaries (arrowheads) and thinned trabeculae (arrows). (H and E, x40)

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Lequesne [1] and Postel and Kerboull [5] were the first to coin the term "rapid destructive hip osteoarthritis" in 1970. Over the next 30 years, subsequent series and reports [2, 3, 6,7,8,9] emphasized the clinical, radiographic, and pathologic findings of this unusual condition.

Typically, patients with rapidly destructive hip osteoarthritis present with rapid destruction of the hip joint within months of the onset of symptoms. In all cases, a rapid clinical course of hip pain is the consistent common clinical symptom. The patients are predominantly women, and the average age at onset (60-70 years) is greater than that of most patients with ordinary osteoarthritis.Go,Go



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Fig. 4A. Rapidly destructive hip osteoarthritis in 73-year-old-woman with right-sided hip pain. Anteroposterior radiograph obtained at onset of symptoms shows moderate superior and lateral joint-space loss.

 


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Fig. 4B. Rapidly destructive hip osteoarthritis in 73-year-old-woman with right-sided hip pain. Anteroposterior radiograph obtained 7 months after A shows major loss of joint space, moderate subchondral sclerosis, and no significant osteophytosis.

 

Initially, conventional radiographs show either no abnormality or mild osteoarthritic changes. Follow-up radiographs, obtained within a few months, show severe progressive joint destruction with focal joint-space narrowing and extensive subchondral bone loss in the femoral head or acetabulum or both. Other characteristic subchondral changes include flattening of the femoral head in a hatchetlike deformity, occasional subluxation, mild bone sclerosis, and a few osteophytes [2, 8, 9]. However, rapid chondrolysis with progressive loss of joint space is the first manifestation of the disease. In 1970, Lequesne [1] proposed a standardized definition of rapid chondrolysis: chondrolysis greater than 2 mm in 1 year or 50% joint-space narrowing in 1 year.

The histologic findings of rapidly destructive hip osteoarthritis are those of osteoarthritis, with severe degenerative changes in articular cartilage [2, 8, 9]. However, absent or minimal osteophyte formation is commonly observed.

In our series, the clinical, radiologic, and pathologic features of rapidly destructive hip osteoarthritis are consistent with previous reports. Eight (67%) of 12 patients were elderly women, and one of 12 patients had bilateral disease. All patients presented with hip pain and rapid progression of symptoms. In all patients, sequential radiographs showed rapid joint destruction with joint-space narrowing and paucity of osteophytes or subchondral bone loss, or both. Radiographically, the differential diagnosis included septic arthritis, inflammatory arthritis, osteonecrosis with secondary osteoarthritis, pyrophosphate-associated destructive arthropathy, or neuropathic osteoarthropathy. However, clinical history, laboratory findings, and successful surgical outcome did not support any of these entities. Furthermore, none of our patients exhibited chondrocalcinosis (pelvis, knees) radiographically or histopathologically. Moreover, pathologic confirmation of osteoarthritis was available in seven cases.

Despite the widespread application of MR imaging as the modality of choice for evaluation of painful hip, we could find only two reports describing the MR appearances of rapidly destructive hip osteoarthritis in the literature in English [2, 3]. Therefore, to our knowledge, our study of 12 patients is the largest series to date. A nonspecific joint effusion was seen in all patients in our series. In nine patients (75%), MR imaging features were consistent with the presence of prominent synovitis in the hip joint (Figs. 1C and 1D). Pathologic examination revealed findings compatible with secondary reactive synovitis in 67% (4/6) of patients. Bock et al. [2] and Rosenberg et al. [8] reported similar histologic findings.

In our study, we commonly observed MR imaging findings consistent with bone marrow edemalike pattern in the femoral head or acetabulum, as reported by Yamamoto and Bullough [3]. Conversely, in the report by Bock et al. [2], findings of conventional T2-weighted MR images of the hip in two patients showed a normal-appearing bone marrow. However, short tau inversion recovery and other fat-suppression techniques used in our study improve the sensitivity of MR imaging in the detection of bone edema.

In four cases (33%), evidence of subchondral fractures was shown on MR imaging (Figs. 3D and 3E), and this was confirmed histopathologically in three cases. Although their reports included only two cases, Yamamoto and Bullough [3] also described the presence of epiphyseal low-signal-intensity lines on MR images. Furthermore, these authors suggested that rapidly destructive hip osteoarthritis may result from a subchondral insufficiency fracture, perhaps related to osteopenia. However, none of their patients underwent measurement of bone mineral density. Because of the retrospective nature of our study, the bone mineral density in our patients was not measured.Go,Go



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Fig. 5A. Rapidly destructive hip osteoarthritis in 73-year-old-woman. Anteroposterior radiograph obtained at onset of symptoms shows moderate superolateral joint-space narrowing with small osteophytes along lateral aspect of acetabulum.

 


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Fig. 5B. Rapidly destructive hip osteoarthritis in 73-year-old-woman. Anteroposterior radiograph obtained 4 months after A shows rapid chondrolysis.

 

In one patient (8%), a bandlike subchondral area showed low signal intensity on images obtained with each of the three sequences (T1-weighted, T2-weighted, and contrast-enhanced T1-weighted MR images) (Figs. 4C and 4D). Zanetti et al. [10] reported that subchondral areas of low signal intensity on both T1- and T2-weighted MR images were composed mainly of abnormal tissue (40% necrotic remodeled trabeculae, 12% bone marrow fibrosis, and 9% bone marrow necrosis) and of smaller proportions of several histologic abnormalities. In our series, the patient with the bandlike subchondral area did not undergo biopsy.

In 10 (83%) of 12 patients, cystlike subchondral defects were more commonly seen at the weight-bearing areas (Figs. 1C and 1D). Pathologic examination showed evidence of mucoid degeneration or granulation tissue that may correspond to regions of high signal intensity on T2-weighted and gadolinium-enhanced T1-weighted MR images.

In 33% of patients, focal signal abnormalities were detected in the adjacent soft tissues (Fig. 5C). The significance of these findings is uncertain. Such signal intensity alterations are not necessarily synonymous with septic arthritis. However, the radiologist should be aware of this potentially misleading MR imaging feature of rapid destructive hip osteoarthritis.

The histologic features observed in our series—nonspecific severe degenerative changes with few marginal osteophytes and no evidence of primary osteonecrosis, pannus formation, and crystal deposition—are similar to those observed by previous authors [1, 2, 7, 8]. Yamamoto and Bullough [3] also described the presence of granulomatous lesions in the bone marrow and suggested that such foci of fragmented bone and articular cartilage debris were characteristic findings in rapidly destructive hip osteoarthritis. In our series, histology did not show evidence of these findings. This type of lesion, however, has been reported to be especially prominent in the advanced stages of rapidly destructive hip osteoarthritis [3].

The precise pathogenesis of rapidly destructive hip osteoarthritis remains unclear. Direct drug toxicity and the analgesic effect of non-steroidal antiinflammatory drugs, especially indomethacin, were first incriminated in the development of rapidly destructive hip osteoarthritis (analgesic hip), but their contributory effect was subsequently challenged in the literature [5]. Some investigators [2, 6, 9] implicated intraarticular deposition of hydroxyapatite crystal as a cause for rapidly destructive hip osteoarthritis. However, apatite deposition in rapidly destructive hip osteoarthritis is a nonspecific and rare finding, and its presence in synovial fluid as a primary or secondary factor in joint damage is still debated. Komiya et al. [11] found that bone resorptive factors such as proteolytic enzymes and cytokines in joint fluid could play a role in rapid chondrolysis. Recently, a proposed cause for rapidly destructive hip osteoarthritis involved subchondral insufficiency fracture of the femoral head [3]. In this regard, the presence of hypointense fracture lines in our study (four cases with histologic confirmation in three) is noteworthy. However, if the concept of subchondral fracture can explain joint destruction, the mechanism of rapid chondrolysis in rapidly destructive hip osteoarthritis remains uncertain. Many factors that may contribute to the disease should probably be considered.

Our study has two major limitations. First, it is a retrospective study with an inherent selection bias. We believe our results merit reporting, however, because the MR imaging findings of this uncommon condition have not been published widely. A second shortcoming is that the pathologic examination was available in only seven patients. In our series as in others [1, 2, 8], we based our diagnoses on accepted clinical and radiologic criteria that were correlated with histologic findings by past investigators [2, 8].

In summary, the diagnosis of rapidly destructive hip osteoarthritis generally is based on a quick progression of hip pain and on radiographs showing rapid chondrolysis. However, various causes of hip joint destruction must be included in the differential diagnosis, especially in the initial phase of rapidly destructive hip osteoarthritis; MR imaging can be valuable in the evaluation of such disorders. Therefore, radiologists should be aware of MR imaging findings in patients with rapidly destructive hip osteoarthritis that can overlap other diagnostic entities. The key MR imaging features include an extensive bone marrow edemalike pattern in the femoral head and neck, femoral head flattening, and cystlike subchondral defects. Additional findings include epiphyseal low-signal-intensity lines, bandlike areas of low signal intensity in the subchondral bone of the femoral head, and focal signal abnormalities in the adjacent soft tissues on short tau inversion recovery, fat-suppressed T2-weighted, or fat-suppressed gadolinium-enhanced T1-weighted MR images.


Acknowledgments
 
We thank Marnix van Holsbeeck of Henry Ford Hospital, Detroit, MI, for reviewing this manuscript.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Lequesne M. Rapid destructive coxarthritis [in French]. Rhumatologie 1970;2:51 -63
  2. Bock GW, Garcia A, Weisman MH, et al. Rapidly destructive hip disease: clinical and imaging abnormalities. Radiology 1993;186:461 -466[Abstract/Free Full Text]
  3. Yamamoto T, Bullough PG. The role of subchondral insufficiency fracture in rapid destruction of the hip joint. Arthritis Rheum 2000;43:2423 -2427[Medline]
  4. Mitchell DG, Rao V, Dalinka M, et al. MRI of joint fluid in the normal and ischemic hip. AJR 1986;246:1215 -1218
  5. Postel M, Kerboull M. Total prosthetic replacement in rapidly destructive arthrosis of the hip joint. Clin Orthop 1970;72:138 -144[Medline]
  6. Doherty M, Holt M, MacMillan P, Watt I, Dieppe P. A reappraisal of "analgesic hip." Ann Rheum Dis 1986;45:272 -276[Abstract/Free Full Text]
  7. Depuyt F, Van Holsbeeck M. Rapidly destructive coxarthrosis: case study and review of the literature [in Dutch]. J Belge Radiol 1990;73:207 -210[Medline]
  8. Rosenberg ZS, Shankman S, Steiner GC, Kastenbaum DK, Norman A, Lazansky MG. Rapid destructive osteoarthritis: clinical, radiographic, and pathologic features. Radiology 1992;182:213 -216[Abstract/Free Full Text]
  9. Lawrance JAL, Athanasou NA. Rapidly destructive hip disease. Skeletal Radiol 1995;24:639 -641[Medline]
  10. Zanetti M, Bruder E, Romero J, Hodler J. Bone marrow edema pattern in osteoarthritic knees: correlation between MR imaging and histologic findings. Radiology 2000;215:835 -840[Abstract/Free Full Text]
  11. Komiya S, Inoue A, Sasaguri Y, Minamitani K, Morimatsu M. Rapidly destructive arthropathy of the hip: studies on bone resorptive factors in joint fluid with a theory of pathogenesis. Clin Orthop 1992;284:273 -282

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