Introduction

The diagnosis of posterior tibial tendon (PTT) dysfunction is often made by history and physical findings alone [1, 2]. However, clinical findings may occasionally be confusing, making the diagnosis a challenge, especially in acute or subacute presentations [3, 4]. Early recognition of PTT dysfunction is critical in preventing irreversible deformity and disability [4]. Imaging of the symptomatic PTT has proven to be a valuable tool in diagnosis, as well as in surgical and treatment planning [5].

MR imaging has been established as the “gold standard” for detection of ankle tendon abnormalities [2, 3, 4, 5, 6, 9]. Several authors have reported on the high accuracy of MR imaging in detecting ankle tendon tears [6, 7, 9, 10]. Recently, numerous studies have documented the effectiveness of sonography (US) as an alternative diagnostic tool for investigating pathology of the PTT [3, 11, 12, 13, 14, 15]. The superficial location of the PTT makes it well suited for imaging by high-resolution US. The development of linear-array high-frequency transducers makes it possible to produce high-resolution images that can display inner tendon structure [6, 16, 7, 18].

The purpose of this preliminary study was to compare US and MR imaging of PTT pathology in patients with PTT dysfunction.

Patients and methods

This study was performed on 18 patients who were examined over a 3-year period, with clinical symptoms of PTT dysfunction. All 18 patients subsequently underwent US and MR imaging within the same day. Four patients who had bilateral symptoms had bilateral studies done. The results of the US examinations were not used for clinical management, but solely for the purposes of this study. All the subjects were women, whose ages ranged from 39 to 86 years, with a mean age of 61 years. All patients presented with symptoms and signs of PTT dysfunction, and a history of chronic ankle pain of greater than 6 weeks’ duration.

Patient histories and physical examinations were performed by the same orthopedic surgeon, who specializes in foot and ankle surgery. Classic clinical findings were utilized as a standard reference, using the staging system of PTT dysfunction of Johnson and Strom [19]. This type of examination has been considered to be an acceptable standard of reference in prior studies of the PTT [7, 20, 21, 22]. Clinically, 16 of the 22 tendons had stage II, III, or IV dysfunction, and were thus considered to have high clinical suspicion for either a partial or full-thickness tear. The other 6 tendons had stage I dysfunction.

US examinations were performed in real time by the same sonologist experienced in musculoskeletal US. All contralateral asymptomatic ankles were scanned for use as a comparison. Static images were all retrospectively interpreted in consensus by the original sonologist as well as a second experienced sonologist who specializes in musculoskeletal US. Although the sonologists were not masked to the symptomatic ankle, they were masked to the clinical staging and the results of the MR examinations. Each examination was performed using a 10 MHz linear-array transducer with a commercially available ultrasound unit (ATL Ultramark 9-HDI, Bothell, Wash.). During the examination, subjects were in the prone or lateral decubitus position. The PTT was imaged in two segments: above and behind the medial malleolus, starting approximately 8 cm superior to the medial malleolus; and between the medial malleolus and the insertion of the PTT on the tarsal navicular. Once the PTT was imaged longitudinally, sequential transverse images (perpendicular to the long axis of the tendon) were obtained. The adjacent flexor digitorum longus tendon was used as a visual comparison in this projection.

Diagnostic criteria on US were as follows. Complete PTT tear was defined as marked disruption of the fibrillary pattern of the tendon, such that tendon continuity was no longer maintained. Partial PTT tear was defined as a linear hypoechoic disruption of the fibrillary pattern not involving the entire tendon thickness. PTT tendinosis was defined as focal or diffuse tendon thickening accompanied by heterogeneous echotexture; hypoechoic foci in the PTT were called tendinosis rather than tear if they were rounded in shape rather than linear, and showed no overt disruption of the fibrillary pattern.

MR examinations were performed on only the symptomatic ankles. Four patients had bilateral studies. All examinations were retrospectively interpreted in consensus by two musculoskeletal radiologists who were masked to the clinical staging of the ankles along with the US findings. All MR imaging was performed using a 1.5 T scanner (Signa; GE Medical Systems, Milwaukee, Wis.) with an extremity coil around the ankle (field of view 14–18 cm). The protocol consisted of imaging in sagittal, axial, and coronal planes; the axial plane was defined as being parallel to the long axis of the foot. Two sets of axial images were obtained. One was intermediate-weighted to optimize the signal-to-noise ratio: proton density fast spin echo (FSE) using a TR/TE (effective) of 2500–3800/34–38 ms, an echo train length of 4, slice thickness 4 mm, skip 1 mm, and a matrix of 256×256 with 2 signals averaged. The other axial sequence consisted of a fat-suppressed T2-weighted FSE sequence that was acquired with a TR/TE (effective) of 3000–6000/60–90 ms, an echo train length of 8, slice thickness of 4 mm, skip 1 mm, and a matrix of 256×192 with 2–3 signals averaged. Coronal images were acquired using the same T2-weighted FSE technique. Sagittal spin echo T1-weighted images (TR/TE=400–700/8–14, slice thickness 3 mm, skip 1 mm, matrix 256×256, 2 signals averaged) and sagittal fast spin echo inversion recovery images (TR/TE/TI=2000–4000/40–60/150 ms, an echo train length of 8, slice thickness 4 mm, skip 1 mm, matrix 256×192, 3 signals averaged) were also acquired. Contrast was not used in any examination.

Diagnostic criteria for MR imaging were as follows. Complete PTT tear was defined as complete discontinuity of the tendon with a fluid gap. Partial PTT tear was defined as intratendinous signal approaching that of fluid on fluid-sensitive sequences. PTT tendinosis was defined as focal thickening or thinning of the tendon, or intratendinous signal less than that of fluid on fluid-sensitive sequences.

The results of the clinical, US, and MR examinations were compared. The study was completed according to the protocol approved by our Institutional Review Board. Informed consent was obtained from all subjects.

Results

Of the 22 ankle studies, US demonstrated tears of the posterior tibial tendon in 8 ankles (8 partial tears) compared with 12 tears (11 partial tears; 1 complete tear) diagnosed by MR imaging. Breakdown by clinical staging is as follows:

  • Of the 6 stage I ankles, neither US nor MR imaging diagnosed any tears.

  • Of the 11 stage II ankles, US diagnosed partial tears of the PTT in 6 ankles. MR imaging also diagnosed partial tears in the same 6 ankles (Fig. 1). In the remaining 5 stage II tendons, US diagnosed tendinosis of the PTT in 2 ankles and reported 3 normal tendons. However, MR imaging identified partial tears in the 2 ankles that were read as tendinosis by US (Fig. 2). The 3 tendons that were read as normal on US demonstrated tendinosis on MR imaging.

    Fig. 1A–C
    figure 1

    A 60-year-old woman with stage II PTT dysfunction, and partial PTT tear seen on sonography and MR imaging. A Axial and B longitudinal sonographic images of right PTT at the level of distal tibia (T) demonstrate linear hypoechoic partial tear (arrows). C Axial fast spin-echo fat-suppressed T2-weighted MR image (6000/72) of the right PTT shows partial disruption of the fibers of the tendon near its insertion, indicated by foci of fluid signal intensity (arrow)

    Fig. 2A–C
    figure 2

    A 73-year-old woman with stage II PTT dysfunction, and tendinosis seen on sonography and MR imaging. A Axial sonographic image of the left PTT at the level of distal tibia (T) demonstrates a rounded hypoechoic abnormality (arrowheads) occupying the majority of the tendon circumference. B Longitudinal sonographic image at the level of the distal tibia (T) shows that the superficial fibers of the PTT are diffusely hypoechoic (arrows) but otherwise intact, consistent with severe tendinosis C Axial fast spin-echo proton density-weighted (2200/20) MR image shows a thickened, tendinotic distal PTT (arrow)

  • Of the 5 stage III ankles, US diagnosed partial tears of the PTT in 2 ankles. MR imaging demonstrated partial tears in the same 2 ankles. Of the 3 remaining stage III ankles, US diagnosed tendinosis of the PTT in 1 ankle and reported 2 normal tendons. MR imaging also identified a partial tear in the ankle that was read as tendinosis by US, and diagnosed tendinosis in an ankle that was reported normal by US. In one of the stage III cases, MR imaging demonstrated a complete tear of the PTT where US only visualized a partial tear (Fig. 3).

    Fig. 3A–D
    figure 3

    An 83-year-old woman with stage III PTT dysfunction. Serial axial MR images demonstrated a complete PTT tear that was interpreted as partial on sonography. A Axial fast spin-echo fat-suppressed T2-weighted MR image (4800/72) of the left PTT superior to the ankle joint shows thickening of the PTT (arrow) near the myotendinous junction. B T2-weighted MR image (4800/72) at the level of the ankle joint shows fluid signal (arrow) in the normal location of the PTT, next to the flexor digitorum longus tendon (arrowhead). C T2-weighted MR image (4800/72) inferior to the ankle joint shows revisualization of a thickened PTT (arrow) anterior to the flexor digitorum longus tendon (arrowhead). D Corresponding longitudinal sonogram of the left PTT obtained at and just below the medial malleolus shows a thickened tendon (arrow) with peritendinous fluid (asterisk). Arrowhead demonstrates the tear that was interpreted as partial on ultrasonography but complete on MR imaging

Previous studies demonstrate that US and MR findings of partial tear and tendinosis are quite comparable and differentiating the two does not affect management [6, 17]. Therefore, the data were then categorized into three groups: normal, tendinosis/partial tear, and complete tear. Based on these categories, the findings of the MR and US examinations were concordant in 6 of 6 stage I tendons (100%), 8 of 11 stage II tendons (73%), and 3 of 5 stage III tendons (60%). Overall, the findings of the MR and US examinations were concordant in 17 of the 22 ankles (77%) (Table 1).

Table 1 Concordance between the US and MR imaging findings based on the clinical stage of PTT dysfunction

Discussion

Although diagnostic staging of PTT dysfunction remains primarily clinical, imaging studies in select patients are necessary for treatment planning [5]. PTT dysfunction refers to a broad spectrum of pathology that may produce similar signs and symptoms. These include tendon avulsion from its navicular insertion, intrasubstance tendon tear, partial tendon tear, and tenosynovitis without tear [5, 21, 23, 24]. There are other potential causes of acquired flatfoot in the adult that are not secondary to PTT dysfunction. These include tarsal coalition, inflammatory arthropathy, neuropathic arthropathy, tarsometatarsal osteoarthritis, neuromuscular disease, and traumatic ligamentous disruption of the mid-foot [20, 25, 26]. The various pathologies may at times be indistinguishable by clinical findings and plain radiographs, making the diagnosis a challenge [21, 23]. In addition, due to the natural progression of the disorder, early recognition of dysfunction is critical in preventing irreversible deformity and disability [4, 15, 25]. Therefore, imaging of the symptomatic PTT has proven to be a valuable tool in diagnosis, as well as in surgical planning [2, 5, 10, 18].

MR imaging has been established as the current imaging gold standard for detection of ankle tendon abnormalities [2, 6, 7, 8, 9]. In 1988, Rosenberg, et al. [10] reported an MR sensitivity of 95%, specificity of 100%, and an accuracy of 96% in detecting tears of the PTT. Numerous authors have since documented the benefits of MR imaging for preoperative planning for ankle tendon reconstructive surgery [2, 5, 7, 8, 9, 10]. MR imaging is useful in localizing the site and extent of rupture, which can aid in the operative approach [5]. However, MR imaging has its limitations. Khoury et al. reported that MR imaging characteristics of tendinosis and partial tear overlap [6]. Degenerative posterior tibial tendons are infrequently seen as MR signal abnormality, and most appear normal [17, 27]. Secondary signs, such as medial tubercle hypertrophy and the appearance of an accessory navicular bone, are often necessary to diagnose subtle partial tears with confidence [7, 28, 29]. A recent study by Rockett et al. could not duplicate the sensitivity and accuracy of MR imaging in detecting ankle tendon tears that was previously recorded by Rosenberg et al. [10, 13].

High-resolution US is another imaging option that can depict PTT pathology [3, 11, 12, 13, 14, 15, 16, 30, 31, 32]. The recent vast improvement in US technology and the development of high-frequency transducers has allowed for superior image resolution and quality. The individual fibrils of a superficial tendon such as the PTT can be visualized with a spatial resolution of less than 0.1 mm in vitro [17, 33], and US is thus far superior to MR imaging at evaluating inner tendon ultrastructure [11, 16, 17, 18, 33]. Several authors in recent years have confirmed that US evaluates PTT pathology with high accuracy [3, 11, 12, 13, 14, 15]. A review of the literature revealed three comparisons of US and MR imaging in evaluating the PTT. Rockett et al. examined 15 posterior tibial tendons with US and MR imaging, and compared the results with surgical findings. US was found to be more accurate than MR imaging, with 100% sensitivity, 90% specificity, and 94% accuracy. In comparison, MR imaging had 23% sensitivity, 100% specificity, and 66% accuracy [13]. These results were supported by those of Gerling et al., who showed that US and MR imaging performed at the same level in evaluating PTT tears; in that study, US demonstrated 69% sensitivity, 81% specificity, and 72% accuracy in comparison with a 73% sensitivity, 69% specificity, and 72% accuracy for MR imaging [34]. Premkumar et al. recently performed a comparative study of 44 posterior tibial tendons with US and MR imaging [35]. The sensitivity and specificity for diagnosing tendinopathy with US was 80% and 90% respectively when compared to MR imaging, and 90% and 80% when diagnosing peritendinitis. However, this study did not look specifically at PTT tears [35].

In an attempt to replicate the results of these recent studies, we performed a study that compared MR imaging and US for PTT evaluation. US compared favorably with MR imaging, the current imaging “gold standard.” Both examinations were consistent in identifying PTT pathology in 17 of 22 cases (77%), and were in agreement in all of the stage I ankles. In evaluating the stage II and III ankles, all discrepancies between US and MR imaging involved differentiating tendinosis from partial tears, and partial tears from complete tears. This result was not surprising, considering that previous studies have shown that the US and MR findings of partial tear and tendinosis overlap, and thus at times cannot be differentiated from each other [6, 17]. Moreover, the distinction between tendinosis and partial tear may not be of clinical significance since patients with partial tears, tendinosis, or tenosynovitis of the PTT are managed similarly. More importantly, these conditions need to be differentiated from complete tears, as treatment may be different. In our one case where MR imaging identified a complete tear that was reported as a partial tear on US, the management of the patient was not affected because the clinical findings were more consistent with partial tear.

This study was limited by the small sample size, so that the findings should be considered only as preliminary. Furthermore, there was no surgical proof since all of our patients were treated conservatively, and MR imaging is an imperfect gold standard. It is conceivable that in some cases when there were discrepant findings between US and MR imaging, US may actually have been correct. A true prospective study with surgical correlation and/or outcome analysis could better address this issue.

To summarize, in this study US compared favorably with MR imaging for imaging PTT pathology. There was complete agreement in all clinically stage I ankles. For clinical stages II and III, although MR imaging detected more tears, these tendons were all interpreted as abnormal on US, and clinical management was therefore not altered. US offers a more convenient and less expensive alternative to MR imaging for detecting PTT tears.