Journal List > J Korean Med Sci > v.33(52) > 1109514

Lee, Kim, Chung, Lee, and Koo: Causes of Chronic Hip Pain Undiagnosed or Misdiagnosed by Primary Physicians in Young Adult Patients: a Retrospective Descriptive Study

Abstract

Background

Hip pain is a common musculoskeletal complaint in general practice. Although comprehensive diagnostic approach on hip pain is mandatory for adequate treatment, un- or mis-diagnosis is not rare in primary care. The aim of this study was to analyze descriptively un- or mis-diagnosed hip pain cases referred from primary care to a tertiary hospital, especially in young adults ≤ 50 years old.

Methods

We retrospectively analyzed a consecutive cohort of 150 patients (≤ 50 years old) with chronic hip pain (≥ 6 weeks), which was not diagnosed or misdiagnosed based on the information provided on the referral form.

Results

Overall an average 32 cases/month were referred due to hip pain without a diagnosis or with an incorrect diagnosis. Among them, 150 patients were enrolled in this study and 146 (97.3%) could be allocated to a specific disease by using data from routine clinical practice. Four common final diagnoses were femoroacetabular impingement (FAI) syndrome (55.3%), hip dysplasia (HD, 13.3%), referred pain from the lumbar spine (9.3%), and spondyloarthritis (SpA, 7.3%). In patients with FAI syndrome, 37 (44.0%) had pincer-type FAI and 33 (39.8%) had combined-type. Although the pain site or gender was not tightly clustered, the distribution of final diagnosis was significantly different according to hip pain location or gender. Especially, SpA or HD was not observed in younger women subgroup or elder men subgroup, respectively, when stratified by the mean age of participants.

Conclusion

Most (> 80%) young patients with hip pain, a difficult issue to diagnosis for many primary physicians, had FAI syndrome, HD, spine lesions, and SpA. This study could give a chance to feedback information about cases with un- or mis-diagnosed hip pain, and it suggests that primary physicians need to be familiar with the diagnostic approach for these 4 diseases.

Graphical Abstract

jkms-33-e339-abf001

INTRODUCTION

Although the prevalence of hip pain is different according to various definitions and tends to be lower than that of knee pain,12 hip pain is a common musculoskeletal complaint in general practice. An accurate diagnosis of hip pain is mandatory for providing adequate treatment and to retard the disease progression to end-stage degenerative stage of the hip. The etiology or diagnostic approach for hip pain have been extensively reviewed by many experts.345
Because the hip joint is structurally complex and too deeply buried to access in physical examination, hip pain remains still a difficult issue to evaluate for most primary care clinicians.6 Additionally, the recent development of the concept of femoroacetabular impingement (FAI) syndrome as well as a long list of the causes of hip pain could pose a diagnostic challenge in daily clinical care.35 To date, diagnostic algorithm for hip pathologies has been focused mainly in the pediatric or elderly population.6 However, diagnostic approach has received less attention and has not been established yet in young and middle-aged adults without childhood-specific hip disorders or prevalent osteoarthritis (OA). Based on such background, primary physicians could not be familiar with the diagnosis of hip pain in young and middle-aged adults.
An analysis of cases with un- or mis-diagnosed hip pain would give a chance to feedback information to the referred physicians and could improve their ability to diagnose and manage hip pain. Therefore, the purpose of this study was to analyze descriptively un- or mis-diagnosed hip pain cases referred from primary care to a tertiary hospital, especially in young adults ≤ 50 years old.

METHODS

From January 2013 to August 2016, a total of 2,680 patients were referred to our hip clinic by primary physicians. Among the referred patients with hip pain, we retrospectively enrolled adult patients (≥ 16-year-old) who were not diagnosed or misdiagnosed based on the information submitted on the referral form (n = 1,398; average 32 case/month). The exclusion criteria were as follows: 1) a history of hip surgery, 2) age > 50 years at the time of referral, and 3) pain duration < 6 weeks (Fig. 1). Finally, we identified 150 patients who met the inclusion and exclusion criteria. They included 66 (44.0%) men and 84 (56.0%) women. Clinical characteristics of study subjects are summarized in Table 1. Based on the referral form, a specific diagnosis was not made at the referral in 118 (78.7%) patients.
Fig. 1

Flow chart of patient enrollment.

jkms-33-e339-g001
Table 1

Clinical characteristics of study subjects (n = 150)

jkms-33-e339-i001
Characteristics Values
Gender (men/women) 66 (44.0)/84 (56.0)
Average age, yr 37.8 (16–50)
Average symptom duration, mon 18.5 (2–241)
Hip pain location
Anterior 65 (43.3)
Posterior 44 (29.3)
Lateral 18 (12.0)
Anterior & lateral 7 (4.7)
Anterior & posterior 16 (10.7)
Bilaterality of hip pain
Unilateral (right-side/left-sided) 57 (38.0)/50 (33.3)
Bilateral 52 (28.7)
Impression provided by primary physicians
Unspecified 118 (78.7)
Soft tissue lesionsa 15 (10.0)
Hip arthritis or synovitis 12 (8.0)
Lumbar disc herniation 3 (2.0)
Nerve entrapment syndromeb 2 (1.3)
Data are presented as mean (ranges) or number (%).
aIncluded bursitis, strain or sprain, and tendinitis; bMeralgia paresthetica.
In our hip clinic, referred patients are seen by two hip surgeons who have provided specialized orthopedic care for hip conditions for 26 and 10 years, respectively. At the first seeing of patient, we ask patients to locate the site of their pain by their index finger. After a through history and focused physical examination of hip joint and/or lumbar spine, we routinely check baseline hip (standing anterior-posterior [AP], Dunn, and translateral views) and lumbosacral radiographs (standing AP, lateral, and flexion/extension views) in all patients. We also check additional radiographs, acute phase reactants including erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), human leukocyte antigen (HLA)-B27, computed tomography (CT) or magnetic resonance imaging (MRI), if further investigations are necessary according to initial impressions. In case suspicious of an underlying rheumatic disorder, who has inflammatory peripheral arthralgia, inflammatory back pain, or extra-articular manifestations,7 the patient is consulted to rheumatology department and finally diagnosed in cooperation with rheumatologists.
In February and March 2018, the medical records and images were thoroughly reviewed by the 2 hip surgeons and 1 rheumatologist who has practiced for 18 years. We collected demographic and clinical data including symptom duration, pain location, and diagnosis of hip pain. Hip pains were classified into three locations; 1) anterior (inguinal or groin region) pain, 2) lateral (trochanteric region) pain, and 3) posterior (buttock, sacroiliac [SI] joint or ischial tuberosity region) pain. Reviewed images included hip and lumbosacral spine radiographs, CT, or MRI. The diagnosis of enrolled patients was made on the basis of clinical features, radiographs and/or laboratory tests by consensus. We tried to select the most explainable cause of their symptom as the final diagnosis, but seven patients had two diagnoses (Table 2).
Table 2

Final diagnosis of un- or mis-diagnosed cases with hip pain

jkms-33-e339-i002
Variables No. (%)
FAI 83 (55.3)a
HD 20 (13.3)a
Spine problems 14 (9.3)a
SpA 11 (7.3)
Ischiogluteal bursitis 5 (3.3)
Undetermined 4 (2.7)
Others
OA 3 (2.0)a
Snapping hip syndrome, extra-articular 3 (2.0)a
Proximal hamstring strain 3 (2.0)
ONFH 2 (1.3)
Calcifying tendinitis 2 (1.3)a
Synovial chondromatosis 2 (1.3)
Trochanteric bursitis 2 (1.3)a
Meralgia paresthetica 1 (0.7)
Insufficiency fracture 1 (0.7)
Osteoid osteoma 1 (0.7)
FAI = femoroacetabular impingement, HD = hip dysplasia, SpA = spondyloarthritis, OA = osteoarthritis, ONFH = osteonecrosis of the femoral head.
aIncluded patients with one or more diagnosis (2 patients with FAI and HD, 2 with FAI and spine problems, 1 with FAI with OA, 1 with FAI with calcifying tendinitis, and 1 with snapping hip syndrome with trochanteric bursitis).
A diagnosis of FAI syndrome was made by motion- or position-related pain in the hip or groin, positive provocative impingement test, and characteristic radiographic findings.8 The characteristic radiographic findings for FAI syndrome included an alpha angle > 55°, acetabular over-coverage (center edge [CE] angle > 39°), herniation pit, or retroverted acetabulum signs (cross over sign, ischial spine sign, or posterior wall sign).89 Additionally, an anterior pincer-type lesion was defined by the presence of retroverted acetabulum and a lateral pincer-type lesion was identified by measuring the lateral CE angle (> 39°).10 An anterior cam-type lesion was defined by alpha angle measurement (> 55°) and a lateral cam-type lesion was by a pistol grip deformity. Moreover, FAI syndrome was classified into pincer, cam, or combined-types according.
Hip dysplasia (HD) was defined as Wiberg's CE angle < 20°.11 The diagnosis of osteonecrosis of the femoral head (ONFH) was made according to Association Research Circulation Osseous (ARCO) classification system.12 Also, the diagnosis of spondyloarthritis (SpA) was made based on the Assessment of SpondyloArthritis international Society (ASAS) criteria.13

Statistical analysis

All continuous variables were described as means with ranges (minimum–maximum). For comparisons of the distribution of categorical variables the Pearson's χ2 or Fisher's exact test was employed. Independent t-test or one-way analysis of variance was used to analyze difference in the difference of continuous variables. Statistical analyses were performed using SPSS for Windows version 20 (IBM Corp., New York, NY, USA) and P < 0.05 was considered statistically significant.

Ethics statement

The study protocol was approved by the Institutional Review Board (Seoul National University Bundang Hospital, IRB No. B-1710/426-104) and the requirement to obtain written informed consent was waived due to the retrospective design of this study.

RESULTS

Anterior hip was the most common location of the hip pain (43.3%); and posterior hip was the second most common site (29.3%) (Table 1). The distribution of pain in the right and left hips was comparable (38.0% vs. 33.3%) and approximately a third of patients had bilateral hip pain (28.7%). The mean symptom duration was 13.8 (range, 2–96) months for FAI syndrome, 25.8 (2–120) months for HD, 24.3 (5–60) months for SpA, and 16.6 (2–48) months for ischiogluteal bursitis. Thirty-seven (25.7%) of the total patients reported a symptom duration of 24 months or more.
In this study, the most common final diagnosis was FAI syndrome (55.3%), which was followed by HD (13.3%), referred pain from the lumbar spine (9.3%), SpA (7.3%), and ischiogluteal bursitis (3.3%) (Table 2). Among 83 patients with FAI syndrome, HD (n = 2), lumbar spine problems (n = 2), OA (n = 1), and calcifying tendinitis (n = 1) were concurrently diagnosed in 6 patients.
The relationship between the hip pain location and major final diagnoses was shown in Fig. 2 using a heat map: the diagnosis was significantly related with the pain location (P < 0.001). Most patients with FAI syndrome or HD complained of anterior hip pain but those with spine problems, SpA, or ischiogluteal bursitis had posterior hip pain. But the pain sites were not tightly clustered and were variable in each disease, except for ischiogluteal bursitis.
Fig. 2

Heat map representing the frequency of hip pain location according to the final diagnosis.

FAI = femoroacetabular impingement, HD = hip dysplasia, SpA = spondyloarthritis.
aSpine problems included referred pain from spinal stenosis and herniated intervertebral disc in the lumbar spine.
jkms-33-e339-g002
Even when stratified into two age subgroups (16–37 and 38–50 years) according to the mean age of the study subjects, the frequency of FAI syndrome was the highest among the final diagnoses in both subgroups (52.9% in younger and 57.3% in elder subgroups). Younger subgroup tended to have higher prevalence of SpA (72.7% vs. 27.3%). When subgrouped by gender, the distribution of the diagnosis was significantly different (P < 0.001). Men patients were more likely to have SpA (90.9% vs. 9.1%) than women. However, HD (94.4% vs. 5.6%) was more prevalent in women. As a result, the women to men ratio was 17:1 for HD and 1:10 for SpA. The frequency of final diagnoses based on gender and age subgroups was summarized in Fig. 3. When study subjects were categorized into younger women or men and elder women or men subgroups, the prevalence of each final diagnosis was significantly different (P < 0.001). Interestingly, SpA or HD was not observed in younger women subgroup or elder men subgroup, respectively.
Fig. 3

The distribution of final diagnosis according to gender and age groups.

FAI = femoroacetabular impingement, HD = hip dysplasia, SpA = spondyloarthritis.
aSpine problems included referred pain from spinal stenosis and herniated intervertebral disc in the lumbar spine.
jkms-33-e339-g003
Of 83 patients with FAI syndrome, 37 (44.0%) had pincer-type and 33 (39.8%) had combined-type FAI (Table 3). Most patients with pincer FAI (27/37, 73.0%) showed anterior pincer-type lesions and 8 (61.5%) of 13 cam FAI had both anterior and lateral cam-type lesions. Moreover, the combination of anterior pincer-type and both anterior and lateral cam-type lesions was mainly observed in combined-type FAI. Pincer FAI was more frequently found in women (30/37, 65.2%) and combined-type FAI was more prevalent in men (23/33, 69.7%; P < 0.001).
Table 3

Distribution of FAI lesions (n = 83)

jkms-33-e339-i003
Variables Cam-type lesions, No. (%) Subtotal, No. (%)
Absence Anterior type Lateral type Both types
Pincer-type lesions
Absence 2 3 8 13 (15.7)
Anterior type 27 4a 3a 18a 52 (62.7)
Lateral type 7 1a 0a 5a 13 (15.7)
Both types 3 0a 1a 1a 5 (6.0)
Subtotal 37 (44.0) 7 (8.3) 7 (8.3) 32 (38.6) 83 (100)
FAI = femoroacetabular impingement.
aThe numbers on gray background correspond to those of subjects with combined type FAI.
SpA was found in 11 patients in this study: 10 (90.9%) patients were HLA-B27 positive and 4 (36.4%) had elevated CRP levels (> 0.05 mg/dL). Non-inflammatory spine problems included lumbar intervertebral disc herniation (n = 8) and spinal stenosis (n = 6). Primary hip OA was observed in only 3 (2.0%) patients. Two patients did not have any history of congenital hip disease, trauma or inflammatory arthropathy but one patient had underlying combined-type FAI syndrome. They all showed hip OA with Tonnis grade ≥ 2.14

DISCUSSION

The diagnostic accuracy and treatment modality of arthritic or non-arthritic hip disease in young patients have been rapidly evolving. This shift has been facilitated by the improvement of our understanding about the functional anatomy of the hip, and the advancement in MRI technology has broadened the differential diagnosis of hip pain. However, many of young adult patients with hip pain have nonspecific symptoms, vague findings in the physical examination, and normal imaging studies.15 Therefore, identifying the source and mechanism of the pain can be difficult.
The current study analyzed the causes of hip pain un- or mis-diagnosed by primary physicians. Various final diagnoses were established in 146 (97.3%) subjects by using data from routine clinical practice at a tertiary hospital. The most common diagnosis was FAI syndrome (55.3%), followed by HD (13.3%), spine problems (9.3%), SpA (7.3%), and ischiogluteal bursitis (3.3%). Ultimately, un- or misdiagnosed hip pain resulted from 4 diseases of FAI syndrome, HD, spine problem, and SpA in 80% of our cases.
Although the concept of FAI was introduced in the 1930s, increasing attention has been paid over ten years in accordance with the popularization of arthroscopic treatment.8 The FAI syndrome is characterized by decreased clearance and abnormal contact between the femoral head-neck junction and the acetabular rim.1617 As the hip flexes and rotates, the front of the ball hits the front of the socket causing a collision known as an “impingement.” Over time, repeated collisions of the ball with the front of the socket can tear the labrum and damage the adjacent cartilage, leading to prearthritic hip pain and secondary OA.1617 The reported prevalence of FAI syndrome is highly variable (1% to 75%) according to the different diagnostic criteria, study populations, and morphologic features of interest.181920 Even FAI-related morphologies can be commonly found in asymptomatic subjects.21 Despite of these findings, FAI-related morphologies significantly increases risk to develop hip OA and are related with hip pain associated with activity.212223 Our study showed that a majority of cases where primary clinicians missed a diagnosis had FAI syndrome. It suggests that more effort has to be made to impart the concept of FAI syndrome to primary physicians.
Among 3 types of FAI-related morphologies, cam or combined-type has been considered more clinically significant lesions in view of symptom or cartilage damage.2425 However, in our study, about 40% of patients with FAI syndrome showed radiographic findings of pincer morphology. Our patients were highly selected because they were composed of cases referred without a specific diagnosis, and the prevalence of 3 types of FAI syndrome might not be comparable to that previously reported. Additionally, all our patients with pincer lesion had symptom and physical examination findings compatible with FAI syndrome and also had no otherwise explainable cause for their symptom. Because the diagnosis of FAI syndrome should be made clinically, but not radiographically,826 primary physicians should be familiar with its clinical features to avoid a delayed diagnosis.
Hip pain in FAI syndrome is commonly located in the inguinal or groin area (anterior hip region) but can be described as pain in the posterior and/or lateral hip regions,1527 as shown in the current study. On physical examination, an important maneuver is the impingement test that is a sensitive screening test for patients with acetabular labral disease and impingement.815 If a patient reports groin pain when passively placing the hip in flexion, adduction, and internal rotation, the patient has a positive impingement test. A recent study suggested that either groin pain with a positive Flexion-Abduction-External Rotation (FABER) test or the combination of a positive impingement and a positive FABER test could serve as a sensitive test for FAI syndrome.28
In this study, the second most common diagnosis was HD, that is involved in 20% to 40% of patients with hip OA.293031 Generally, most HD cases are diagnosed through a screening at birth and during infancy. But some of patients could be diagnosed with HD in adolescence or early adulthood. Several population-based studies reported the prevalence of HD was 3.3% to 7.3% in adult population.323334 Even though adolescent or adult-diagnosed dysplasia and infantile-diagnosed dysplasia may be separate identities, both subsets are women-predominant diseases; 7:1 in adolescent or adult-diagnosed dysplasia and 49:1 in infantile-diagnosed dysplasia.35 In the present study, the women to men ratio was also as high as 17:1. Therefore, primary physicians always consider HD as a cause of hip pain even in women adults. In case of borderline dysplasia (20° ≤ CE angle < 25°), depth history taking, physical examination and thorough radiographic evaluation are essential to properly diagnosis.
It is well known that hip pain can be referred from the lumbar spine and spine problems were the third most common condition in our subjects. The subgroup complained of posterior hip pain alone (57.1%) or both anterior and posterior hip pain (21.4%). Birnbaum et al.36 showed the sensory innervation of the hip joint; the anterior, anteromedial, posteromedial, and posterolateral area of the joint capsule are innervated by the branches of obturator, femoral, sciatic, and superior gluteal nerves (i.e., sensory nerves from L2 to S1), respectively. Additionally, in the Rotterdam Study, de Schepper et al.37 found that the disk space narrowing at the L1/L2 or L2/L3 spine level was significantly associated with hip pain. On the contrary, Nakamura et al.3839 reported that some patients with OA secondary to HD (17%) or ONFH (8%) had referred pain to the low back. These findings suggest that primary physicians do not forget spine or hip lesions as a cause of patient's hip or lumbar pain, respectively.
SpA is a group of chronic inflammatory disease primarily affecting the axial skeleton and enthesis and its prevalence has been reported to be 0.4% to 1.3%.40 SpA has been traditionally considered a men-dominant disease, although the gender difference is much reduced in SpA defined by the ASAS criteria.40 In ankylosing spondylitis, the reported prevalence of hip disease ranges from 19% to 36% and is much higher in patients with a younger disease onset.41 The current study also showed that SpA patients were almost men patients (90.9%), especially younger subgroup (80.0%). A Korean multicenter study also showed that the men to women ratio was 6.1:1 and hip involvement is more prevalent in men patients with ankylosing spondylitis.42 Therefore, in men young patients with hip pain, SpA-focused laboratory evaluation including HLA-B27 or a SI joint radiograph could successfully lead to its diagnosis.
There are several limitations to address in this study. First, because our study was retrospective, important diagnostic clues for other uncommon causes could be lost. For example, abductor sprain or tendinopathy, piriformis syndrome, and adhesive capsulitis of hip were not encountered in our study. Differential diagnosis should also consider other hip pathologies in a real-world clinical setting. Nevertheless, it could not affect the overall context of our study since common diseases are more likely to be more often diagnosed than uncommon ones. Second, this study was performed at a single tertiary referral hospital and the prevalence of hip pathologies is different among nations or races.4344 Also, the limitations include the small sample size and the lack of independent data to replicate our results. Therefore, our results could not be generalized to all populations and more studies are warranted in other populations.
Conclusively, our study showed that top 4 diseases causing hip pain included FAI syndrome, HD, spine problems, and SpA in cases un- or mis-diagnosed by primary physicians. Additionally, meticulous history taking, and physical examinations were useful to determine the cause of hip pain in most cases. Primary care giver should add the diseases into the list of differential diagnosis when assessing patients with chronic hip pain.

Notes

Disclosure The authors have no potential conflicts of interest to disclose.

Author Contributions

  • Conceptualization: Lee YJ, Chung SW, Lee YK, Koo KH.

  • Data curation: Kim SH, Chung SW, Lee YK.

  • Formal analysis: Kim SH, Chung SW, Lee YK, Koo KH.

  • Investigation: Lee YK, Koo KH.

  • Methodology: Lee YJ, Kim SH, Lee YK, Koo KH.

  • Writing - original draft: Lee YJ, Chung SW, Lee YK, Koo KH.

  • Writing - review & editing: Lee YJ, Lee YK, Koo KH.

References

1. Thiem U, Lamsfuß R, Günther S, Schumacher J, Bäker C, Endres HG, et al. Prevalence of self-reported pain, joint complaints and knee or hip complaints in adults aged ≥ 40 years: a cross-sectional survey in Herne, Germany. PLoS One. 2013; 8(4):e60753.
crossref
2. Suka M, Yoshida K. The national burden of musculoskeletal pain in Japan: Projections to the year 2055. Clin J Pain. 2009; 25(4):313–319.
3. Battaglia PJ, D'Angelo K, Kettner NW. Posterior, lateral, and anterior hip pain due to musculoskeletal origin: a narrative literature review of history, physical examination, and diagnostic imaging. J Chiropr Med. 2016; 15(4):281–293.
crossref
4. Karrasch C, Lynch S. Practical approach to hip pain. Med Clin North Am. 2014; 98(4):737–754. xi
crossref
5. Skendzel JG, Weber AE, Ross JR, Larson CM, Leunig M, Kelly BT, et al. The approach to the evaluation and surgical treatment of mechanical hip pain in the young patient: AAOS exhibit selection. J Bone Joint Surg Am. 2013; 95(18):e133.
6. Poultsides LA, Bedi A, Kelly BT. An algorithmic approach to mechanical hip pain. HSS J. 2012; 8(3):213–224.
crossref
7. Ventura I, Reid P, Jan R. Approach to patients with suspected rheumatic disease. Prim Care. 2018; 45(2):169–180.
crossref
8. Griffin DR, Dickenson EJ, O'Donnell J, Agricola R, Awan T, Beck M, et al. The Warwick Agreement on femoroacetabular impingement syndrome (FAI syndrome): an international consensus statement. Br J Sports Med. 2016; 50(19):1169–1176.
crossref
9. Mineta K, Goto T, Wada K, Tamaki Y, Hamada D, Tonogai I, et al. CT-based morphological assessment of the hip joint in Japanese patients: association with radiographic predictors of femoroacetabular impingement. Bone Joint J. 2016; 98-B(9):1167–1174.
10. Tannast M, Siebenrock KA, Anderson SE. Femoroacetabular impingement: radiographic diagnosis--what the radiologist should know. AJR Am J Roentgenol. 2007; 188(6):1540–1552.
crossref
11. Wiberg G. Studies on dysplastic acetabula and congenital subluxation of the hip joint with special reference to the complication of osteoarthritis. Acta Chir Scand. 1939; 83:Suppl 58. 53–68.
12. Gardeniers J. A new international classification of osteonecrosis of the ARCO committee on terminology and classification. ARCO Newsl. 1992; 4(4):41–46.
13. Rudwaleit M, van der Heijde D, Landewé R, Akkoc N, Brandt J, Chou CT, et al. The Assessment of SpondyloArthritis International Society classification criteria for peripheral spondyloarthritis and for spondyloarthritis in general. Ann Rheum Dis. 2011; 70(1):25–31.
crossref
14. Tönnis D, Behrens K, Tscharani F. A modified technique of the triple pelvic osteotomy: early results. J Pediatr Orthop. 1981; 1(3):241–249.
crossref
15. Clohisy JC, Beaulé PE, O'Malley A, Safran MR, Schoenecker P. AOA symposium. Hip disease in the young adult: current concepts of etiology and surgical treatment. J Bone Joint Surg Am. 2008; 90(10):2267–2281.
16. Ganz R, Parvizi J, Beck M, Leunig M, Nötzli H, Siebenrock KA. Femoroacetabular impingement: a cause for osteoarthritis of the hip. Clin Orthop Relat Res. 2003; (417):112–120.
17. Lavigne M, Parvizi J, Beck M, Siebenrock KA, Ganz R, Leunig M. Anterior femoroacetabular impingement: part I. Techniques of joint preserving surgery. Clin Orthop Relat Res. 2004; 418:61–66.
18. Dickenson E, Wall PD, Robinson B, Fernandez M, Parsons H, Buchbinder R, et al. Prevalence of cam hip shape morphology: a systematic review. Osteoarthritis Cartilage. 2016; 24(6):949–961.
crossref
19. Mascarenhas VV, Rego P, Dantas P, Morais F, McWilliams J, Collado D, et al. Imaging prevalence of femoroacetabular impingement in symptomatic patients, athletes, and asymptomatic individuals: a systematic review. Eur J Radiol. 2016; 85(1):73–95.
crossref
20. van Klij P, Heerey J, Waarsing JH, Agricola R. The prevalence of cam and pincer morphology and its association with development of hip osteoarthritis. J Orthop Sports Phys Ther. 2018; 48(4):230–238.
crossref
21. Frank JM, Harris JD, Erickson BJ, Slikker W 3rd, Bush-Joseph CA, Salata MJ, et al. Prevalence of femoroacetabular impingement imaging findings in asymptomatic volunteers: a systematic review. Arthroscopy. 2015; 31(6):1199–1204.
crossref
22. Kowalczuk M, Yeung M, Simunovic N, Ayeni OR. Does femoroacetabular impingement contribute to the development of hip osteoarthritis? A systematic review. Sports Med Arthrosc Rev. 2015; 23(4):174–179.
crossref
23. Kopec JA, Cibere J, Li LC, Zhang C, Barber M, Qian H, et al. Relationship between physical activity and hip pain in persons with and without cam or pincer morphology: a population-based case-control study. Osteoarthritis Cartilage. 2017; 25(7):1055–1061.
crossref
24. Larson CM, Safran MR, Brcka DA, Vaughn ZD, Giveans MR, Stone RM. Predictors of clinically suspected intra-articular hip symptoms and prevalence of hip pathomorphologies presenting to sports medicine and hip preservation orthopaedic surgeons. Arthroscopy. 2018; 34(3):825–831.
crossref
25. Guo Y, Zhang H, Qian H, Wilson DR, Wong H, Barber M, et al. Association of femoroacetabular impingement and delayed gadolinium-enhanced magnetic resonance imaging of cartilage: a population-based study. Arthritis Care Res (Hoboken). 2017; 70(8):1160–1168.
crossref
26. Cunningham DJ, Paranjape CS, Harris JD, Nho SJ, Olson SA, Mather RC 3rd. Advanced imaging adds little value in the diagnosis of femoroacetabular impingement syndrome. J Bone Joint Surg Am. 2017; 99(24):e133.
crossref
27. Clohisy JC, Baca G, Beaulé PE, Kim YJ, Larson CM, Millis MB, et al. Descriptive epidemiology of femoroacetabular impingement: a North American cohort of patients undergoing surgery. Am J Sports Med. 2013; 41(6):1348–1356.
28. Tijssen M, van Cingel RE, de Visser E, Hölmich P, Nijhuis-van der Sanden MW. Hip joint pathology: relationship between patient history, physical tests, and arthroscopy findings in clinical practice. Scand J Med Sci Sports. 2017; 27(3):342–350.
crossref
29. Aronson J. Osteoarthritis of the young adult hip: etiology and treatment. Instr Course Lect. 1986; 35:119–128.
30. Harris WH. Etiology of osteoarthritis of the hip. Clin Orthop Relat Res. 1986; (213):20–33.
crossref
31. Solomon L. Patterns of osteoarthritis of the hip. J Bone Joint Surg Br. 1976; 58(2):176–183.
crossref
32. Engesæter IO, Laborie LB, Lehmann TG, Fevang JM, Lie SA, Engesæter LB, et al. Prevalence of radiographic findings associated with hip dysplasia in a population-based cohort of 2081 19-year-old Norwegians. Bone Joint J. 2013; 95-B(2):279–285.
crossref
33. Umer M, Thambyah A, Tan WT, Das De S. Acetabular morphometry for determining hip dysplasia in the Singaporean population. J Orthop Surg (Hong Kong). 2006; 14(1):27–31.
crossref
34. Jacobsen S, Sonne-Holm S, Søballe K, Gebuhr P, Lund B. Hip dysplasia and osteoarthrosis: a survey of 4151 subjects from the Osteoarthrosis Substudy of the Copenhagen City Heart Study. Acta Orthop. 2005; 76(2):149–158.
35. Lee CB, Mata-Fink A, Millis MB, Kim YJ. Demographic differences in adolescent-diagnosed and adult-diagnosed acetabular dysplasia compared with infantile developmental dysplasia of the hip. J Pediatr Orthop. 2013; 33(2):107–111.
crossref
36. Birnbaum K, Prescher A, Hessler S, Heller KD. The sensory innervation of the hip joint--an anatomical study. Surg Radiol Anat. 1997; 19(6):371–375.
37. de Schepper EI, Damen J, Bos PK, Hofman A, Koes BW, Bierma-Zeinstra SM. Disk degeneration of the upper lumbar disks is associated with hip pain. Eur Spine J. 2013; 22(4):721–726.
crossref
38. Nakamura J, Oinuma K, Ohtori S, Watanabe A, Shigemura T, Sasho T, et al. Distribution of hip pain in osteoarthritis patients secondary to developmental dysplasia of the hip. Mod Rheumatol. 2013; 23(1):119–124.
crossref
39. Nakamura J, Konno K, Orita S, Hagiwara S, Shigemura T, Nakajima T, et al. Distribution of hip pain in patients with idiopathic osteonecrosis of the femoral head. Mod Rheumatol. 2017; 27(3):503–507.
crossref
40. Bakland G, Nossent HC. Epidemiology of spondyloarthritis: a review. Curr Rheumatol Rep. 2013; 15(9):351.
crossref
41. Vander Cruyssen B, Vastesaeger N, Collantes-Estévez E. Hip disease in ankylosing spondylitis. Curr Opin Rheumatol. 2013; 25(4):448–454.
crossref
42. Jung YO, Kim I, Kim S, Suh CH, Park HJ, Park W, et al. Clinical and radiographic features of adult-onset ankylosing spondylitis in Korean patients: comparisons between males and females. J Korean Med Sci. 2010; 25(4):532–535.
crossref
43. Lavy CB, Msamati BC, Igbigbi PS. Racial and gender variations in adult hip morphology. Int Orthop. 2003; 27(6):331–333.
crossref
44. Dudda M, Kim YJ, Zhang Y, Nevitt MC, Xu L, Niu J, et al. Morphologic differences between the hips of Chinese women and white women: could they account for the ethnic difference in the prevalence of hip osteoarthritis? Arthritis Rheum. 2011; 63(10):2992–2999.
crossref
TOOLS
ORCID iDs

Yun Jong Lee
https://orcid.org/0000-0001-7615-8611

Sang-Hwan Kim
https://orcid.org/0000-0002-8009-9594

Sang Wan Chung
https://orcid.org/0000-0002-3449-696X

Young-Kyun Lee
https://orcid.org/0000-0001-6564-4294

Kyung-Hoi Koo
https://orcid.org/0000-0001-5251-2911

Similar articles