Results and discussion

Pathology in GI organs can be imaged with EUS using anatomical landmarks for orientation. In patients without gastric surgery, all landmarks can be located in at least 90% of cases. However, scanning all organs completely would take more than an hour. Thus, in any given examination, certain unrelated structures or areas need not be recorded, if the focus is a specific anatomical site.

Table 13.2 - Accuracy (%) of GI tumour staging and resectability with EUS and CT.
EUS CT
Oesophagus T stage8560
N stage8055
M stage7070
Resectability8055
GastricT stage8040
N stage7550
M stage7575
Resectability8070
PancreasT stage9050
N stage7550
M stage6565
Resectability8040
Biliary SystemT stage8545
N stage6050
M stage8585
Resectability8050
RectumT stage8570
N stage8055
M stage-75
Values are median estimates in % from references in text.

Table 13.2 shows the median accuracy of TNM staging and assessment of resectability for EUS compared to CT scan for various major GI neoplasms. 4 Errors in T stage occur because EUS cannot always distinguish between neoplastic tissue and benign inflammation or fibrosis. Because high frequency Sound waves have a penetration depth of only 2-4 cm from the probe, optimal focus of vessels or structures around a tumour larger than 5 cm may not always be achieved, and vessel or organ involvement may be missed.

Errors in N stage can occur for similar reasons. 4,29,52,55 A malignant node can appear to have benign characteristics because micrometastases have not yet caused parenchymal changes that can be seen sonographically. Criteria for lymph node boundaries and echogenicity appear to overlap less than those for size and shape (Table 13.3). Most metastatic lymph nodes are <10mm. By relying almost exclusively on size to evaluate N stage, CT has been insensitive for neoplastic regional lymph nodes. In contrast, because most lymph nodes >10 mm are usually neoplastic, specificity is good when CT is positive. Unlike CT scan, size resolution is not a limitation for EUS. Lymph nodes >3 mm can be found easily. However, even though EUS is superior to other imaging methods in differentiating malignant from inflammatory benign lyph nodes, criteria (Table 13.3) overlap and still require improvement.

In a prospective series of 1000 patients where EUS was performed in an office setting, the major complication rate was 0.2% (Snady H, unpublished observations, 1996). Two perforations occurred in patients with oesophageal tumours, one related to preEUS dilation of the tumour. Transient laryngospasm occurred in a third patient. In a worldwide retrospective survey of 42,105 patients,67 the "major complication rate was also reported to be low (0.05%). Two-thirds of upper GI EUS complications occurred in patients with oesophageal strictures. In 10 of 13 perforations, oesophageal dilation had been performed immediately prior to EUS. Mortality within 30 days of EUS occurred in only I of 42,105 patients surveyed, and was related to one such perforation. Therefore, aggressive dilation of all oesophageal stricture at the time of EUS is not recommended.

Table 13.3 - Criteria to differentiate malignant and inflammatory lymph nodes.
MalignantBenign
BoundriesSharpIndistinct
Echogenicity *Echo-poor
Homogeneous
Echo-rich
Non-homogeneous
ShapeRoundIrregular
Size>10mm<5mm
* Criteria are useful only for frequencies of 7.0MHz or greater.

EUS provides detailed images of the GI tract. Clinical applications continue to expand. Proper use of equipment and understanding sound wave properties will minimize errors of the method. Appreciation of how artifacts produce certain changes in tissues improves the operator's facility not only to distinguish the true image, but also to use the artifact to interpret pathology and make a diagnosis. Shadowing and enhancement artifacts are frequently useful in this regard. Section thickness and reverberation artifacts are generally more difficult to interpret and use constructively. The sonographer can be seriously misled by artifacts, which if properly recognized can be used to reveal and inform.

Improvements in correlations of sonographic findings to histology will continue to improve with further studies. Development of various agents to enhance or change sound wave characteristics of tissues and differentiate normal and pathological states will become valuable. Further human and animal studies will continue to establish and clarify parameters that will decrease interobserver variability.36-38,47 The role of EUS in selection of appropriate treatment will depend upon alternatives available for amelioration of symptoms and improvement of quality of life, survival and outcome.4,14 Utility of EUS will continue to increase with application of major advances in ultrasound technology.68


Acknowledgement

The author is grateful to Laurel Kiefer for editorial and graphic assistance.

References