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AJR 2002; 178:1445-1449
© American Roentgen Ray Society


Original Report

Sonography of Ankle Ganglia with Pathologic Correlation in 10 Pediatric and Adult Patients

Robert Ortega1, David P. Fessell1, Jon A. Jacobson1, John Lin1,2, Marnix T. van Holsbeeck1 and Curtis W. Hayes1

1 Department of Radiology, University of Michigan Hospitals, 1500 E. Medical Center Dr., Ann Arbor, MI 48109-0326.
2 Valley Radiology, Ltd., 5322 W. Northern Ave., Glendale, AZ 85301.
3Department of Radiology, Henry Ford Hospital, 2799 W. Grand Blvd., Detroit, MI 48202.

Received June 26, 2001; accepted after revision December 12, 2001.

 
Presented at the annual meeting of the American Roentgen Ray Society, Washington, DC, May 2000.

Address correspondence to D. P. Fessell.


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. We describe the sonographic imaging characteristics of ankle ganglia with pathologic correlation in 10 patients.

CONCLUSION. Foot and ankle ganglia exhibit a spectrum of sonographic appearances from round and completely anechoic masses to hypoechoic, multilobulated, multiseptated masses with dependent debris. All the ganglionic cysts examined in our study showed posterior acoustic enhancement without solid nodules on sonography.


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Sonography is increasingly being used for assessment of foot and ankle abnormalities. Ganglionic cysts are the most common soft-tissue masses in the foot and ankle [1]. These cysts can be asymptomatic or associated with symptoms such as pain, weakness, swelling, osseous erosion, joint impairment, or tarsal tunnel syndrome [2]. Using sonography, radiologists can rapidly and efficiently diagnose a cystic ankle mass and distinguish it from a solid or complex mass that may require further evaluation. In addition, sonography can reveal the extent of a ganglionic cyst and its relationship to the surrounding structures and can show an origin from a specific joint or tendon sheath. This report illustrates the sonographic appearance of ankle ganglionic cysts with pathologic correlation in 10 patients. To our knowledge, this report is the first sonographic description of a series of ankle ganglionic cysts with pathologic correlation.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
A database search identified 1,234 consecutive reports of musculoskeletal sonographic examinations of the lower extremity (below the knee) between April 1995 and May 2000 from one institution, and another database search of a separate institution's records identified 361 additional consecutive reports of foot and ankle sonographic examinations between August 1996 and July 2000. These reports were individually assessed to determine whether surgery on the foot or ankle was subsequently performed. All cases in which a mass lesion was surgically resected were noted and correlated with the pathology report, which yielded 10 cases of pathologically proven ankle ganglia. Institutional review board approval was obtained for this study from both institutions.

Sonographic examinations were performed (model HDI 3000 or 5000, Advanced Technology Laboratories, Bothell, WA; or model 5200, Acoustic Imaging, Phoenix, AZ) using linear array transducers ranging from 7.5 to 12 MHz. Sonography was performed by one of seven radiologists experienced in musculoskeletal sonography.

Sonograms from the 10 cases were retrospectively evaluated by consensus of three radiologists for the following sonographic characteristics of the mass: echogenicity; posterior acoustic enhancement; and presence or absence of septations, lobulation, or a solid soft-tissue component. Hypoechoic was defined as less echogenic than surrounding muscle with diffuse low-level echoes within the lesion. Anechoic was defined as sonolucent except for linear septations. From the original sonography reports, the sonographic diagnosis was noted as well as any communication with a specific joint or tendon sheath. The original report was used because more information is available to the sonographer during real-time scanning than is contained in the static images available for retrospective review.

The size of each mass and thickness of any septations were retrospectively measured by one radiologist. Measurements were made using cursor measurements on the film or manual calipers. The use of Doppler evaluation was also noted from the sonograms and sonography reports. Operative reports were available in seven cases (70%), and the origin of any communicating neck found at surgery was noted. Interpretation of the original pathologic specimens was performed by one of nine pathologists. All 10 patients were female; patient age at surgery ranged from 12 to 60 years (mean, 39 years). The time between sonography and surgery ranged from 1 to 377 days (mean, 69 days).


Results
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Materials and Methods
Results
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The retrospective consensus interpretations of the sonographic characteristics of the 10 cases are summarized in Table 1. The sonographic and pathologic features are illustrated in Figures 1A,1B,2A,2B,3A,3B,4A,4B,5A,5B. The ganglionic cysts were anechoic in eight (80%) of the 10 cases (Figs. 1A,1B,2A,2B,3A,3B and 5A,5B) and hypoechoic in two (20%) (Fig. 4A,4B); all 10 showed posterior acoustic enhancement. The two ganglionic cysts that were characterized as hypoechoic were at the anechoic end of the hypoechoic spectrum. Five of the 10 masses had septations (Figs. 2A,2B, 3A,3B, and 5A,5B), and three of the 10 masses had lobulated borders (Figs. 2A,2B, 3A,3B, and 4A,4B). No solid nodules were definitely identified by the consensus review, and none were reported in the original sonography reports. One of the masses had an echogenic dependent component, consistent with dependent debris (Fig. 5A,5B). Color Doppler evaluation was performed in four of the 10 cases. No evidence of internal blood flow was noted in any of the masses. No Doppler waveforms were obtained. The size of the ganglionic cysts in the greatest dimension ranged from 0.6 to 4.0 cm. The maximal thickness of any septation was 2 mm. In six of the 10 patients, a history of pain associated with the mass was noted.


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TABLE 1 Sonographic Characteristics of Pathologically Proven Ankle Ganglia in 10 Patients

 


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Fig. 1A. 29-year-old woman with mass in anterolateral soft tissues of right ankle who presented with increasing pain of 3 months' duration. Longitudinal sonogram shows anechoic mass within subcutaneous tissue. No communication with joint or tendon sheath was identified. Posterior acoustic enhancement (arrowheads) can be seen. Reverberation artifact is visible at superficial border of cyst (small arrows). Large arrow = ganglion cyst.

 


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Fig. 1B. 29-year-old woman with mass in anterolateral soft tissues of right ankle who presented with increasing pain of 3 months' duration. Photomicrograph of ganglionic cyst shows dense fibrous wall (arrows) surrounding well-defined central cavity (asterisk). (H and E, x2)

 


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Fig. 2A. 48-year-old woman with mass in lateral soft tissues of ankle. Longitudinal sonogram shows anechoic mass (arrows) with septation (arrowhead).

 


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Fig. 2B. 48-year-old woman with mass in lateral soft tissues of ankle. Photomicrograph of mass shows portion of dense fibrous wall (arrowheads) with myxoid degeneration (arrows) that surrounds central cystic cavity (asterisk). (H and E, x10)

 


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Fig. 3A. 47-year-old woman with mass in medial soft tissues of right ankle who presented with progressive pain and swelling over 7 months. Longitudinal sonogram shows anechoic mass (arrows) superficial to posterior tibial tendon (small arrowheads) and flexor digitorum longus tendon (large arrowhead).

 


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Fig. 3B. 47-year-old woman with mass in medial soft tissues of right ankle who presented with progressive pain and swelling over 7 months. Transverse sonogram shows anechoic mass (arrows) with lobulation, extending between posterior tibial tendon (small arrowheads) and flexor digitorum longus tendon (large arrowhead).

 


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Fig. 4A. 42-year-old woman with mass on dorsal ankle. Longitudinal sonogram shows mass (arrows) judged to be hypoechoic relative to surrounding muscle by consensus review. Posterior acoustic enhancement is noted as increased hyperechogenicity of talar cortex (arrowheads). Two split screens were aligned for extended field of view in this image. tib = tibial cortex, talus = talar cortex.

 


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Fig. 4B. 42-year-old woman with mass on dorsal ankle. Transverse sonogram shows hypoechoic mass with communication (straight arrows) extending toward lateral subtalar joint (curved arrow) between talus (tal) and calcaneus (cal).

 


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Fig. 5A. 32-year-old woman with mass in anterolateral soft tissues of ankle. Longitudinal sonogram shows anechoic mass (between cursors) with multiple internal septations (arrows).

 


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Fig. 5B. 32-year-old woman with mass in anterolateral soft tissues of ankle. Transverse sonogram shows mass (large straight arrows) with prominent thick septation (small straight arrow). Echogenic component (curved arrow) can be seen along deep border, which is consistent with dependent debris. TRANSV = transverse, MED = medial aspect of mass.

 

The preoperative sonography reports provided the diagnosis of a "ganglion cyst" in seven of the 10 cases. In the remaining three cases, the findings were described as "compatible with a ganglion," "ganglion cyst versus synovial cyst," and "synovial cyst." Compared with the surgical findings, the sonography report correctly identified the source of a communicating neck to a joint in two cases and the absence of any neck in one case (Table 1). In two cases, sonography failed to detect a communication that was noted at surgery, and in two additional cases, sonography suggested the communication originated from a different joint or tendon sheath than was noted at surgery. In three cases, no surgical report was available.

Pathology reports were available in all cases. Pathologic findings showed thin-walled cysts containing mucoid material with adjacent mucinous degeneration, which is characteristic of ganglionic cysts. Neither evidence of a synovial lining or solid nodules nor findings of malignancy were noted in the pathology reports.


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Soft-tissue masses around the foot and ankle are frequently caused by a cystic mass. Ganglionic cysts are thought to result from focal myxomatous degeneration of collagenous tissue or from a communication with a joint or tendon sheath. Ganglionic cysts are typically contain a viscous, gelatinous fluid that is surrounded by a wall composed of a dense, fibrous connective tissue [1]. Lower extremity ganglionic cysts account for an estimated 15-20% of all ganglionic cysts [1]. Foot and ankle ganglionic cysts account for approximately 70% of all surgically treated lower extremity ganglionic cysts. Compared with wrist ganglia, ankle ganglia are more frequently symptomatic [3]; these ganglia may be symptomatic more often because of their larger average size relative to wrist ganglia. As noted in this report and prior studies, foot and ankle ganglia are typically 1-3 cm versus less than 1.5 cm for most wrist ganglia [4, 5].

Prior reports of sonography of ankle ganglia have included case reports, one of which included pathologic correlation [4]. In contrast, wrist ganglia have been studied extensively with sonography, including several reports with pathologic correlation [5,6,7,8]. Ganglia have been reported to be anechoic or hypoechoic in the wrist [6, 9], which is consistent with our findings for ankle ganglia. Reverberation artifact, which produces linear echoes at the superficial border of a ganglionic cyst (Fig. 1A,1B), should not be mistaken for internal echoes. Reverberation can be eliminated with the use of a standoff pad or copious amounts of coupling gel. Wrist ganglia have been described as typically well-defined, round, or oval cysts with smooth or lobulated borders [5, 7]. Lobulated borders were noted in three cases in our study (30%) and can be prominent (Figs. 3A,3B and 4A,4B). Visualization of a communication with a joint or tendon sheath increases the confidence for the diagnosis of a ganglionic cyst and aids surgical planning [8] (Fig. 4A,4B).

Ganglionic cysts typically show posterior acoustic enhancement, as did all the ganglia in this report. Small ganglionic cysts, however, may show little or no enhanced through-transmission. If a ganglionic cyst is located adjacent to cortical bone, posterior acoustic enhancement may not be visualized in the tissues deep in relation to the mass [6]. However, in such cases increased through-transmission can be noted as increased hyperechogenicity of the underlying cortex (Fig. 4A). Angulation of the transducer can also project the posterior enhancement away from the cortex, which aids visualization.

Septations within ganglionic cysts have not been commonly described in wrist ganglia [5,6,7,8]. However, septations are frequently observed in ankle ganglia, as evidenced by five ganglia (50%) in our study. Septations can be multiple and branching (Fig. 5A,5B). It has been suggested that if septations are noted within soft-tissue masses—especially multiple or thick septations, then suspicion for a malignant process should be increased [10].

In four of our cases, there was a discrepancy between the sonographic and surgical findings regarding the presence of a duct or its origin from a specific joint or tendon sheath (Table 1). These discrepancies were likely caused by one or more of the following factors: incomplete sonographic evaluation that did not detect a neck or duct that could have been visualized with sonography; the presence of an extremely thin or fibrosed duct that was imperceptible with sonography; or the presence of a duct that dissected deep in a region where multiple joints or tendon sheaths are present, thus causing confusion as to the exact source. Complete evaluation of the mass with careful attention to the detection of a joint or tendon communication can aid diagnosis. When a duct dissects deep in a region of multiple joints or tendons, caution in attributing the exact source is warranted. If the duct does not contain fluid, as may be the case with a fibrosed or scarred duct, then the likelihood of visualization with sonography is decreased.

The differential diagnosis of a ganglionic cyst includes anechoic or hypoechoic masses. Common anechoic or hypoechoic masses of the foot and ankle include abscesses, seromas, or hypoechoic lipomas. Clinical history and aspiration can aid in the diagnosis of an abscess. A seroma can be indistinguishable from a ganglionic cyst. A lipoma can be confirmed with MR imaging. A variety of benign and malignant masses can appear hypoechoic. Some solid masses with a homogenous cellular composition, such as neurofibromas and melanomas, can appear hypoechoic with increased through-transmission, simulating a debrisfilled cyst [11, 12].

In cases in which gray-scale imaging does not enable definitive diagnosis of a ganglionic cyst, Doppler assessment can aid evaluation. Doppler evaluation was used in four (40%) of 10 of the patients in this retrospective study and was helpful in detecting internal blood flow and defining adjacent vessels. Internal blood flow on Doppler evaluation or the presence of a nodular component raises suspicion for a malignant neoplasm. In such cases, MR imaging, biopsy, or resection can be used to further evaluate the cyst. A peripheral, dependent, linear, echogenic component was seen in one of the 10 cases and likely was caused by dependent debris. Dependent debris can obscure a nodule. Imaging the patient in a new position can shift the location of dependent debris and exclude this possibility.

There are several limitations to this retrospective report. The study is composed of a relatively small number of cases. The inclusion of only pathologically verified cases is a bias; however, pathologic proof is the strongest gold standard and is needed to establish the sonographic appearance with the highest accuracy. All 10 patients in this study were female. However, the appearance of wrist ganglia has not been shown to significantly differ for female versus male patients; moreover, a sex difference in the appearance of ankle ganglia would not be expected.

The sonographic characteristics of the ankle ganglia were determined by a consensus of three radiologists who were not blinded to the findings from the pathologic specimens, and interobserver variability was not calculated. Surgical reports were available in seven of the 10 cases, which limits the correlation between sonography and surgery for the origin of a communicating neck. Variability in the scanning technique of the sonographers and variability in the interpretation of the surgical specimens by the pathologists are also limitations.

This study does not attempt to determine the accuracy of sonography for the detection of ankle ganglia. It is unknown whether there were sonographic false-positive or false-negative cases during the time period included in this study.

In conclusion, foot and ankle ganglia exhibit a spectrum of sonographic appearances from round and completely anechoic masses to hypoechoic, multilobulated, multiseptated masses with dependent debris. All ganglionic cysts showed posterior acoustic enhancement without solid nodules.


References
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Rozbruch SR, Chang V, Bohne WH, Deland JT. Ganglion cysts of the lower extremity: an analysis of 54 cases and review of the literature. Orthopedics 1998;21:141 -148[Medline]
  2. Steiner E, Steinbach LS, Schnarkowski P, Tirman PFJ, Genant HK. Ganglia and cysts around joints. Radiol Clin North Am 1996;34:395 -425[Medline]
  3. Kliman EK, Frieberg A. Ganglion of the foot and ankle. Foot Ankle Int 1982;3:45 -46
  4. Wu KK. Ganglions of the foot. J Foot Ankle Surg 1993;32:343 -347[Medline]
  5. Osterwalder JJ, Widrig R, Stober R, Gachter A. Diagnostic validity of ultrasound in patients with persistent wrist pain and suspected occult ganglion. J Hand Surg Am 1997;22:1034 -1040[Medline]
  6. Hoglund M, Tordai P, Muren C. Diagnosis of ganglions in the hand and wrist by sonography. Acta Radiol 1994;35:35 -39[Medline]
  7. Paivansalo M, Jalovaara P. Ultrasound findings of ganglions of the wrist. Eur J Radiol 1991;13:178 -180[Medline]
  8. De Flavis L, Nessi R, Del Bo P, Calori G, Balconi G. High-resolution ultrasonography of wrist ganglia. J Clin Ultrasound 1987;15:17 -22[Medline]
  9. Cardinal E, Buckwalter KA, Braunstein EM, Mih AD. Occult dorsal carpal ganglion: comparison of US and MR imaging. Radiology 1994;193:259 -262[Abstract/Free Full Text]
  10. Ma LD, McCarthy EF, Bluemke DA, Frassica FJ. Differentiation of benign from malignant musculoskeletal lesions using MR imaging: pitfalls in MR evaluation of lesions with a cystic appearance. AJR 1998;170:1251 -1258[Free Full Text]
  11. Lin JL, Jacobson JA, Hayes CW. Sonographic target sign in neurofibromas. J Ultrasound Med 1999;18:513 -517[Medline]
  12. Nazarian LN, Alexander AA, Kurtz AB, et al. Superficial melanoma metastases: appearances on gray-scale and color Doppler sonography. AJR 1998;170:459 -463[Abstract/Free Full Text]

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